The amphipod crustacean Parhyale hawaiensis is a blossoming model system for studies of developmental mechanisms and more recently regeneration. We have sequenced the genome allowing annotation of all key signaling pathways, transcription factors, and non-coding RNAs that will enhance ongoing functional studies. Parhyale is a member of the Malacostraca clade, which includes crustacean food crop species. We analysed the immunity related genes of Parhyale as an important comparative system for these species, where immunity related aquaculture problems have increased as farming has intensified. We also find that Parhyale and other species within Multicrustacea contain the enzyme sets necessary to perform lignocellulose digestion ('wood eating'), suggesting this ability may predate the diversification of this lineage. Our data provide an essential resource for further development of Parhyale as an experimental model. The first malacostracan genome will underpin ongoing comparative work in food crop species and research investigating lignocellulose as an energy source.https://doi.org/10.7554/eLife.20062.001
The marine crustacean known as Parhyale hawaiensis is related to prawns, shrimps and crabs and is found at tropical coastlines around the world. This species has recently attracted scientific interest as a possible new model to study how animal embryos develop before birth and, because Parhyale can rapidly regrow lost limbs, how tissues and organs regenerate. Indeed, Parhyale has many characteristics that make it a good model organism, being small, fast-growing and easy to keep and care for in the laboratory.
Several research tools have already been developed to make it easier to study Parhyale. This includes the creation of a system for using the popular gene editing technology, CRISPR, in this animal. However, one critical resource that is available for most model organisms was missing; the complete sequence of all the genetic information of this crustacean, also known as its genome, was not available.
Kao, Lai, Stamataki et al. have now compiled the Parhyale genome – which is slightly larger than the human genome – and studied its genetics. Analysis revealed that Parhyale has genes that allow it to fully digest plant material. This is unusual because most animals that do this rely upon the help of bacteria. Kao, Lai, Stamataki et al. also identified genes that provide some of the first insights into the immune system of crustaceans, which protects these creatures from diseases.
Kao, Lai, Stamataki et al. have provided a resource and findings that could help to establish Parhyale as a popular model organism for studying several ideas in biology, including organ regeneration and embryonic development. Understanding how Parhyale digests plant matter, for example, could progress the biofuel industry towards efficient production of greener energy. Insights from its immune system could also be adapted to make farmed shrimp and prawns more resistant to infections, boosting seafood production.https://doi.org/10.7554/eLife.20062.002
Very few members of the Animal Kingdom hold the esteemed position of major model system for understanding living systems. Inventions in molecular and cellular biology increasingly facilitate the emergence of new experimental systems for developmental genetic studies. The morphological and ecological diversity of the phylum Arthropoda makes them an ideal group of animals for comparative studies encompassing embryology, adaptation of adult body plans and life history evolution (Akam, 2000; Budd and Telford, 2009; Peel et al., 2005; Scholtz and Wolff, 2013). While the most widely studied group are Hexapods, reflected by over a hundred sequencing projects available in the NCBI genome database, genomic data in the other three sub-phyla in Arthropoda are still relatively sparse.
Recent molecular and morphological studies have placed crustaceans along with hexapods into a pancrustacean clade (Figure 1A), revealing that crustaceans are paraphyletic (Mallatt et al., 2004; Cook et al., 2005; Regier et al., 2005; Ertas et al., 2009; Richter, 2002). Previously, the only available fully sequenced crustacean genome was that of the water flea Daphnia which is a member of the Branchiopoda (Colbourne et al., 2011). A growing number of transcriptomes for larger phylogenetic analyses have led to differing hypotheses of the relationships of the major pancrustacean groups (Figure 1B) (Meusemann et al., 2010; Regier et al., 2010; Oakley et al., 2013; von Reumont et al., 2012). The genome of the amphipod crustacean Parhyale hawaiensis addresses the paucity of high quality non-hexapod genomes among the pancrustacean group, and will help to resolve relationships within this group as more genomes and complete proteomes become available (Rivarola-Duarte et al., 2014; Kenny et al., 2014). Crucially, genome sequence data is also necessary to further advance research in Parhyale, currently the most tractable crustacean model system. This is particularly true for the application of powerful functional genomic approaches, such as genome editing (Cong et al., 2013; Serano et al., 2015; Martin et al., 2015; Mali et al., 2013; Jinek et al., 2012; Gilles and Averof, 2014).
Parhyale is a member of the diverse Malacostraca clade with thousands of extant species including economically and nutritionally important groups such as shrimps, crabs, crayfish and lobsters, as well as common garden animals like woodlice. They are found in all marine, fresh water, and higher humidity terrestrial environments. Apart from attracting research interest as an economically important food crop, this group of animals has been used to study developmental biology and the evolution of morphological diversity (for example with respect to Hox genes) (Martin et al., 2015; Averof and Patel, 1997; Liubicich et al., 2009; Pavlopoulos et al., 2009), stem cell biology (Konstantinides and Averof, 2014; Benton et al., 2014), innate immunity processes (Vazquez et al., 2009; Hauton, 2012) and recently the cellular mechanisms of regeneration (Konstantinides and Averof, 2014; Benton et al., 2014; Alwes et al., 2016). In addition, members of the Malacostraca, specifically both Amphipods and Isopods, are thought to be capable of 'wood eating' or lignocellulose digestion and to have microbiota-free digestive systems (King et al., 2010; Kern et al., 2013; Boyle and Mitchell, 1978; Zimmer et al., 2002).
The life history of Parhyale makes it a versatile model organism amenable to experimental manipulations (Figure 1C) (Wolff and Gerberding, 2015). Gravid females lay eggs every 2 weeks upon reaching sexual maturity and hundreds of eggs can be easily collected at all stages of embryogenesis. Embryogenesis takes about 10 days at 26°C and has been described in detail with an accurate staging system (Browne et al., 2005). Early embryos display an invariant cell lineage with each blastomere at the 8-cell stage contributing to a specific germ layer (Figure 1D) (Browne et al., 2005; Gerberding et al., 2002). Embryonic and post-embryonic stages are amenable to experimental manipulations and direct observation in vivo (Gerberding et al., 2002; Extavour, 2005; Rehm et al., 2009a, 2009b, 2009c, 2009d; Price et al., 2010; Alwes et al., 2011; Hannibal et al., 2012; Kontarakis and Pavlopoulos, 2014; Nast and Extavour, 2014; Chaw and Patel, 2012; Pavlopoulos and Averof, 2005). These can be combined with transgenic approaches (Pavlopoulos and Averof, 2005; Kontarakis et al., 2011; Kontarakis and Pavlopoulos, 2014; Pavlopoulos et al., 2009), RNA interference (RNAi) (Liubicich et al., 2009) and morpholino-mediated gene knockdown (Ozhan-Kizil et al., 2009), and transgene-based lineage tracing (Konstantinides and Averof, 2014). Most recently the utility of the clustered regularly interspaced short palindromic repeats (CRISPR)/CRISPR-associated (Cas) system for targeted genome editing has been elegantly demonstrated during the systematic study of Parhyale Hox genes (Martin et al., 2015; Serano et al., 2015). This arsenal of experimental tools (Table 1) has already established Parhyale as an attractive model system for biological research.
So far, work in Parhyale has been constrained by the lack of a reference genome and other standardized genome-wide resources. To address this limitation, we have sequenced, assembled and annotated the genome. At an estimated size of 3.6 Gb, this genome represents one of the largest animal genomes tackled to date. The large size has not been the only challenge of the Parhyale genome, that also exhibits some of the highest levels of sequence repetitiveness and polymorphism reported among published genomes. We provide information in our assembly regarding polymorphism to facilitate functional genomic approaches sensitive to levels of sequence similarity, particularly homology-dependent genome editing approaches. We analysed a number of key features of the genome as foundations for new areas of research in Parhyale, including innate immunity in crustaceans, lignocellulose digestion, non-coding RNA biology, and epigenetic control of the genome. Our data bring Parhyale to the forefront of developing model systems for a broad swathe of important bioscience research questions.
The Parhyale genome contains 23 pairs (2n=46) of chromosomes (Figure 2) and with an estimated size of 3.6 Gb, it is currently the second largest reported arthropod genome after the locust genome (Parchem et al., 2010; Wang et al., 2014). Sequencing was performed on genomic DNA isolated from a single adult male taken from a line derived from a single female and expanded after two rounds of sib-mating. We performed k-mer analyses of the trimmed reads to assess the impact of repeats and polymorphism on the assembly process. We analyzed k-mer frequencies (Figure 3A) and compared k-mer representation between our different sequencing libraries. We observed a 93% intersection of unique k-mers among sequencing libraries, indicating that the informational content was consistent between libraries (Source code 1). The k-mer analysis revealed a bimodal distribution of error-free k-mers (Figure 3A). The higher-frequency peak corresponded to k-mers present on both haplotypes (i.e. homozygous regions), while the lower-frequency peak had half the coverage and corresponded to k-mers present on one haplotype (i.e. heterozygous regions) (Simpson and Durbin, 2012). We concluded that the single sequenced adult Parhyale exhibits very high levels of heterozygosity, similar to the highly heterozygous oyster genome (see below).
In order to quantify global heterozygosity and repeat content of the genome we assessed the de-Bruijn graphs generated from the trimmed reads to observe the frequency of both variant and repeat branches (Simpson, 2014) (Figure 3B and C). We found that the frequency of the variant branches was 10x higher than that observed in the human genome and very similar to levels in the highly polymorphic genome of the oyster Crassostrea gigas (Zhang et al., 2012). We also observed a frequency of repeat branches approximately 4x higher than those observed in both the human and oyster genomes (Figure 3C), suggesting that the big size of the Parhyale genome can be in large part attributed to the expansion of repetitive sequences.
These metrics suggested that both contig assembly and scaffolding with mate-pair reads were likely to be challenging due to high heterozygosity and repeat content. After an initial contig assembly we remapped reads to assess coverage of each contig. We observed a major peak centered around 75x coverage and a smaller peak at 150x coverage. Contigs with lower 75x coverage represent regions of the genome that assembled into separate haplotypes and had half the frequency of mapped sequencing reads, reflecting high levels of heterozygosity. This resulted in independent assembly of haplotypes for much of the genome (Figure 3D).
One of the prime goals in sequencing the Parhyale genome was to achieve an assembly that could assist functional genetic and genomic approaches in this species. Different strategies have been employed to sequence highly heterozygous diploid genomes of non-model and wild-type samples (Kajitani et al., 2014). We aimed for an assembly representative of different haplotypes, allowing manipulations to be targeted to different allelic variants in the assembly. This could be particularly important for homology dependent strategies that are likely to be sensitive to polymorphism. However, the presence of alternative haplotypes could lead to poor scaffolding between contigs as many mate-pair reads may not map uniquely to one contig and distinguish between haplotypes in the assembly. To alleviate this problem we used a strategy to conservatively identify pairs of allelic contigs and proceeded to use only one in the scaffolding process. First, we estimated levels of similarity (identity and alignment length) between all assembled contigs to identify independently assembled allelic regions (Figure 3E). We then kept the longer contig of each pair for scaffolding using our mate-pair libraries (Figure 3F), after which we added back the shorter allelic contigs to produce the final genome assembly (Figure 4A).
RepeatModeler and RepeatMasker were used on the final assembly to find repetitive regions, which were subsequently classified into families of transposable elements or short tandem repeats (Source code 2). We found 1473 different repeat element sequences representing 57% of the assembly (Figure 4—source data 1). The Parhyale assembly comprises of 133,035 scaffolds (90% of assembly), 259,343 unplaced contigs (4% of assembly), and 584,392 shorter, potentially allelic contigs (6% of assembly), with a total length of 4.02 Gb (Table 2). The N50 length of the scaffolds is 81,190 bp. The final genome assembly was annotated with Augustus trained with high confidence gene models derived from assembled transcriptomes, gene homology, and ab initio predictions. This resulted in 28,155 final gene models (Figure 4B; Source code 3) across 14,805 genic scaffolds and 357 unplaced contigs with an N50 of 161,819, bp and an N90 of 52,952 bp.
Parhyale has a mean coding gene size (introns and ORFs) of 20 kb (median of 7.2 kb), which is longer than D. pulex (mean: 2 kb, median: 1.2 kb), while shorter than genes in Homo sapiens (mean: 52.9 kb, median: 18.5 kb). This difference in gene length was consistent across reciprocal blast pairs where ratios of gene lengths revealed Parhyale genes were longer than Caenorhabditis elegans, D. pulex, and Drosophila melanogaster and similar to H. sapiens. (Figure 5A). The mean intron size in Parhyale is 5.4 kb, similar to intron size in H. sapiens (5.9 kb) but dramatically longer than introns in D. pulex (0.3 kb), D. melanogaster (0.3 kb) and C. elegans (1 kb) (Figure 5B).
For downstream analyses of Parhyale protein coding content, a final proteome consisting of 28,666 proteins was generated by combining candidate coding sequences identified with TransDecoder (Haas et al., 2013) from mixed stage transcriptomes. Almost certainly the high number of predicted gene models and proteins is an overestimation due to fragmented genes, very different isoforms or unresolved alleles, that will be consolidated as annotation of the Parhyale genome improves. We also included additional high confidence gene predictions that were not found in the transcriptome (Figure 4C). The canonical proteome dataset was annotated with both Pfam, KEGG, and BLAST against Uniprot. Assembly quality was further evaluated by alignment to core eukaryotic genes defined by the Core Eukaryotic Genes Mapping Approach (CEGMA) database (Parra et al., 2007). We identified 244/248 CEGMA orthology groups from the assembled genome alone and 247/248 with a combination of genome and mapped transcriptome data (Figure 4—figure supplement 1). Additionally, 96% of over 280,000 identified transcripts, most of which are fragments that do not contain a large ORF, also mapped to the assembled genome. Together these data suggest that our assembly is close to complete with respect to protein coding genes and transcribed regions that are captured by deep RNA sequencing.
To estimate the level of heterozygosity in genes we first identified transcribed regions of the genome by mapping back transcripts to the assembly. Where these regions appeared in a single contig in the assembly, heterozygosity was calculated using information from mapped reads. Where these regions appeared in more than one contig, because haplotypes had assembled independently, heterozygosity was calculated using an alignment of the genomic sequences corresponding to mapped transcripts and information from mapped reads. This allowed us to calculate heterozygosity for each gene within the sequenced individual (Source code 4). We then calculated the genomic coverage of all transcribed regions in the genome and found, as expected, they fell broadly into two categories with higher and lower read coverage (Figure 6A; Source code 4). Genes that fell within the higher read coverage group had a lower mean heterozygosity (1.09% of bases displaying polymorphism), which is expected as more reads were successfully mapped. Genes that fell within the lower read coverage group had a higher heterozygosity (2.68%), as reads mapped independently to each haplotype (Figure 6B) (Simpson, 2014). Thus, we conclude that heterozygosity that influences read mapping and assembly of transcribed regions, and not just non-coding parts of the assembly.
The assembled Parhyale transcriptome was derived from various laboratory populations, hence we expected to see additional polymorphism beyond that detected in the two haplotypes of the individual male we sequenced. Analysing all genes using the transcriptome we found additional variations in transcribed regions not found in the genome of the sequenced individual. In addition to polymorphisms that agreed with heterozygosity in the genome sequence we observed that the rate of additional variations is not substantially different between genes from the higher (0.88%) versus lower coverage group genes (0.73%; Figure 6C). This analysis suggests that within captive laboratory populations of Parhyale there is considerable additional polymorphism distributed across genes, irrespective of whether or not they have relatively low or high heterozygosity in the individual male we sequenced. In addition the single male we have sequenced provides an accurate reflection of polymorphism of the wider laboratory population and the established Chicago-F strain does not by chance contain unusually divergent haplotypes. We also performed an assessment of polymorphism on previously cloned Parhyale developmental genes, and found some examples of startling levels of variation. (Figure 6—figure supplement 1 and source data 1). For example, we found that the cDNAs of the germ line determinants, nanos (78 SNPS, 34 non-synonymous substitutions and one 6 bp indel) and vasa (37 SNPs, 7 non-synonymous substitutions and a one 6 bp indel) can have more variability within laboratory Parhyale populations than might be observed for orthologs between closely related species (Figure 6—source data 1).
To further evaluate the extent of polymorphism across the genome, we mapped the genomic reads to a set of previously Sanger-sequenced BAC clones of the Parhyale Hox cluster from the same Chicago-F line from which we sequenced the genome of an adult male. (Serano et al., 2015). We detected SNPs at a rate of 1.3 to 2.5% among the BACs (Table 3) and also additional sequence differences between the BACs and genomic reads, confirming that additional polymorhism exists in the Chicago-F line beyond that detected between in the haplotypes of the individual male we sequenced.
Overlapping regions of the contiguous BACs gave us the opportunity to directly compare Chicago-F haplotypes and accurately observe polynucleotide polymorphisms, that are difficult to detect with short reads that do not map when polymorphisms are large, but are resolved by longer Sanger reads. (Figure 7A). Since the BAC clones were generated from a pool of Chicago-F animals, we expected each sequenced BAC to be representative of one haplotype. Overlapping regions between BAC clones could potentially represent one or two haplotypes. We found that the genomic reads supported the SNPs observed between the overlapping BAC regions. We found relatively few base positions with evidence supporting the existence of a third allele. This analysis revealed many insertion/deletion (indels) with some cases of indels larger than 100 base pairs (Figure 7B). The finding that polynucleotide polymorphisms are prevalent between the haplotypes of the Chicago-F is another reason, in addition to regions of high SNP heterozygosity in the genome sequence, for the extensive independent assembly of haplotypes. Taken togther these data mean that special attention will have to be given to those functional genomic approaches that are dependent on homology, such as CRISPR/Cas9 based knock in strategies.
Assessment of conservation of the proteome using BLAST against a selection of metazoan proteomes was congruent with broad phylogenetic expectations. These analyses included crustacean proteomes likely to be incomplete as they come from limited transcriptome datasets, but nonetheless highlighted genes likely to be specific to the Malacostraca (Figure 5C, Figure 5—source data 2). To better understand global gene content evolution we generated clusters of orthologous and paralogous gene families comparing the Parhyale proteome with other complete proteomes across the Metazoa using Orthofinder (Emms and Kelly, 2015) (Figure 5D; Figure 5—source data 3). Amongst proteins conserved in protostomes and deuterostomes we saw no evidence for widespread gene duplication in the lineage leading to Parhyale. We identified orthologous and paralogous protein groups across 16 species with 2900 and 2532 orthologous groups containing proteins found only in Panarthropoda and Arthropoda respectively. We identified 855 orthologous groups that were shared exclusively by Mandibulata, 772 shared by Pancrustacea and 135 shared by Crustacea. There were 9877 Parhyale proteins that could not be assigned to an orthologous group, potentially representing rapidly evolving or lineage specific proteins (Figure 5—source data 1). Amongst these proteins we found 609 proteins (2.1% of the proteome) that had paralogs within Parhyale, suggesting that younger and/or more divergent Parhyale genes have undergone some considerable level of gene duplication events.
Our analysis of shared orthologous groups was equivocal with regard to alternative hypotheses on the relationships among pancrustacean subgroups: 44 groups of orthologous proteins are shared among the multicrustacea clade (uniting the Malacostraca, Copepoda and Thecostraca), 37 groups are shared among the Allocarida (Branchiopoda and Hexapoda) and 49 groups are shared among the Vericrustacea (Branchiopoda and Multicrustacea.
To further analyse the evolution of the Parhyale proteome we examined protein families that appeared to be expanded (z-score >2), compared to other taxa (Figure 5—figure supplement 1, Source code 5). We conservatively identified 29 gene families that are expanded in Parhyale. Gene family expansions include the Sidestep (55 genes) and Lachesin (42) immunoglobulin superfamily proteins as well as nephrins (33 genes) and neurotrimins (44 genes), which are thought to be involved in immunity, neural cell adhesion, permeability barriers and axon guidance (Strigini et al., 2006; Garver et al., 2008; Siebert et al., 2009). Other Parhyale gene expansions include APN (aminopeptidase N) (38 genes) and cathepsin-like genes (30 genes), involved in proteolytic digestion (Deraison et al., 2004).
Components of all common metazoan cell-signalling pathways are largely conserved in Parhyale. At least 13 Wnt subfamilies were present in the cnidarian-bilaterian ancestor. Wnt3 has been lost in protostomes that retain 12 Wnt genes (Prud'homme et al., 2002; Cho et al., 2010-07; Janssen et al., 2010). Some sampled ecdysozoans have undergone significant Wnt gene loss, for example C. elegans has only 5 Wnt genes (Hilliard and Bargmann, 2006). At most 9 Wnt genes are present in any individual hexapod species (Bolognesi et al., 2008), with wnt2 and wnt4 potentially lost before the hexapod radiation (Hogvall et al., 2014). The Parhyale genome encodes 6 of the 13 Wnt subfamily genes; wnt1, wnt4, wnt5, wnt10, wnt11 and wnt16 (Figure 8). Wnt genes are known to have been ancestrally clustered (Holstein, 2012). We observed that wnt1 and wnt10 are linked in a single scaffold (phaw_30.0003199); given the loss of wnt6 and wnt9, this may be the remnant of the ancient wnt9-1-6-10 cluster conserved in some protostomes.
We could identify 2 Fibroblast Growth Factor (FGF) genes and only a single FGF receptor (FGFR) in the Parhyale genome, suggesting one FGFR has been lost in the malacostracan lineage (Figure 8——figure supplement 1). Within the Transforming Growth Factor beta (TGF-) signaling pathway we found 2 genes from the activin subfamily (an activin receptor and a myostatin), 7 genes from the Bone Morphogen Protein (BMP) subfamily and 2 genes from the inhibin subfamily. Of the BMP genes, Parhyale has a single decapentaplegic homologue (Figure 8—source data 2). Other components of the TGF- pathway were identified such as the neuroblastoma suppressor of tumorigenicity (NBL1/DAN), present in Aedes aegypti and Tribolium castaneum but absent in D. melanogaster and D. pulex, and TGFB-induced factor homeobox 1 (TGIF1) which is a Smad2-binding protein within the pathway present in arthropods but absent in nematodes (C. elegans and Brugia malayi;Figure 8—source data 2). We identified homologues of PITX2, a downstream target of the TGF- pathway involved in endoderm and mesoderm formation present in vertebrates and crustaceans (Parhyale and D. pulex) but not in insects and nematodes (Ryan et al., 1998). With the exception of SMAD7 and SMAD8/9, all other SMADs (SMAD1, SMAD2/3, SMAD4, SMAD6) are found in arthropods sampled, including Parhyale. Components of other pathways interacting with TGF- signaling like the JNK, Par6, ROCK1/RhoA, p38 and Akt pathways were also recovered and annotated in the Parhyale genome (Figure 8—source data 2). We identified major Notch signaling components including Notch, Delta, Deltex, Fringe and modulators of the Notch pathway such as Dvl and Numb. Members of the gamma-secretase complex (Nicastrin, Presenillin, and APH1) were also present as well as to other co-repressors of the Notch pathway such as Groucho and CtBP (Nagel et al., 2005).
A genome wide survey to annotate all potential transcription factors (TFs) discovered a total of 1143 proteins with DNA binding domains that belonged to all the major families previously identified. Importantly, we observed a large expansion of TFs containing the zinc-finger (ZF)-C2H2 domain, that was previously observed in a trancriptomic study of Parhyale (Zeng et al., 2011). Parhyale has 699 ZF-C2H2-containing genes (Chung et al., 2002–12], which is comparable to the number found in H. sapiens (Najafabadi et al., 2015), but significantly expanded compared to other arthropod species like D. melanogaster encoding 326 members (Figure 8—source data 1).
The Parhyale genome contains 126 homeobox-containing genes (Figure 9; Figure 8—source data 3), which is higher than the numbers reported for other arthropods (104 genes in D. melanogaster, 93 genes in the honey bee Apis melllifera, and 113 in the centipede Strigamia maritima) (Chipman et al., 2014). We identified a Parhyale specific expansion in the Ceramide Synthase (CERS) homeobox proteins, which include members with divergent homeodomains (Pewzner-Jung et al., 2006). H. sapiens have six CERS genes, but only five with homeodomains (Holland et al., 2007). We observed an expansion to 12 CERS genes in Parhyale, compared to 1–4 genes found in other arthropods (Zhong and Holland, 2011) (Figure 8—figure supplement 2). In phylogenetic analyses all 12 CERS genes in Parhyale clustered together with a CERS from another amphipod Echinogammarus veneris, suggesting that this is recent expansion in the amphipod lineage.
Parhyale contains a complement of 9 canonical Hox genes that exhibit both spatial and temporal colinearity in their expression along the anterior-posterior body axis (Serano et al., 2015). Chromosome walking experiments had shown that the Hox genes labial (lab) and proboscipedia (pb) are linked and that Deformed (Dfd), Sex combs reduced (Scr), Antennapedia (Antp) and Ultrabithorax (Ubx) are also contiguous in a cluster (Serano et al., 2015). Previous experiments in D. melanogaster had shown that the proximity of nascent transcripts in RNA fluorescent in situ hybridizations (FISH) coincide with the position of the corresponding genes in the genomic DNA (Kosman et al., 2004; Ronshaugen and Levine, 2004). Thus, we obtained additional information on Hox gene linkage by examining nascent Hox transcripts in cells where Hox genes are co-expressed. We first validated this methodology in Parhyale embryos by confirming with FISH, the known linkage of Dfd with Scr in the first maxillary segment where they are co-expressed (Figure 10A–A“). As a negative control, we detected no linkage between engrailed1 (en1) and Ubx or abd-A transcripts (Figure 10B - B“,C - C“). We then demonstrated the tightly coupled transcripts of lab with Dfd (co-expressed in the second antennal segment, Figure 10D - D“), Ubx and abd-A (co-expressed in the posterior thoracic segments, Figure 10E - E“), and abd-A with Abd-B (co-expressed in the anterior abdominal segments, (Figure 10F - F“). Collectively, all evidence supports the linkage of all analysed Hox genes into a single cluster as shown in (Figure 10G - G“). The relative orientation and distance between certain Hox genes still needs to be worked out. So far, we have not been able to confirm that Hox3 is also part of the cluster due to the difficulty in visualizing nascent transcripts for Hox3 together with pb or Dfd. Despite these caveats, Parhyale provides an excellent arthropod model system to understand these still enigmatic phenomena of Hox gene clustering and spatio-temporal colinearity, and compare the underlying mechanisms to other well-studied vertebrate and invertebrate models (Kmita and Duboule, 2003).
The ParaHox and NK gene clusters encode other ANTP class homeobox genes closely related to Hox genes (Brooke et al., 1998). In Parhyale, we found 2 caudal (Cdx) and 1 Gsx ParaHox genes. Compared to hexapods, we identified expansions in some NK-like genes, including 5 Bar homeobox genes (BarH1/2), 2 developing brain homeobox genes (DBX) and 6 muscle segment homeobox genes (MSX/Drop). Evidence from several bilaterian genomes suggests that NK genes are clustered together (Pollard and Holland, 2000; Jagla et al., 2001; Luke et al., 2003; Castro and Holland, 2003]. In the current assembly of the Parhyale genome, we identified an NK2-3 gene and an NK3 gene on the same scaffold (phaw_30.0004720) and the tandem duplication of an NK2 gene on another scaffold (phaw_30.0004663). Within the ANTP class, we also observed 1 mesenchyme homeobox (Meox), 1 motor neuron homeobox (MNX/Exex) and 3 even-skipped homeobox (Evx) genes.
Lignocellulosic (plant) biomass is the most abundant raw material on our planet and holds great promise as a source for the production of bio-fuels (Himmel et al., 2007). Understanding how some animals and their symbionts achieve lignocellulose digestion is a promising research avenue for exploiting lignocellulose-rich material (Wilson, 2011; Cragg et al., 2015). Amongst Metazoans, research into the ability to depolymerize plant biomass into useful catabolites is largely restricted to terrestrial species such as ruminants, termites and beetles. These animals rely on mutualistic associations with microbial endosymbionts that provide cellulolytic enzymes known as glycosyl hydrolases (GHs) (Duan et al., 2009; Warnecke et al., 2007) (Figure 11). Much less studied is lignocellulose digestion in aquatic animals despite the fact that lignocellulose represents a major energy source in aquatic environments, particularly for benthic invertebrates (Distel et al., 2011). Recently, it has been suggested that the marine wood-boring Isopod Limnoria quadripunctata and the amphipod Chelura terebrans may have sterile microbe-free digestive systems and they produce all required enzymes for lignocellulose digestion (King et al., 2010; Green Etxabe, 2013; Kern et al., 2013). Significantly, these species have been shown to have endogenous GH7 family enzymes with cellobiohydrolase (beta-1,4-exoglucanase) activity, previously thought to be absent from animal genomes. From an evolutionary perspective, it is likely that GH7 coding genes were acquired by these species via horizontal gene transfer from a protist symbiont.
Parhyale is a detrivore that can be sustained on a diet of carrots (Figure 11C), suggesting that they too may be able to depolymerize lignocellulose for energy (Figure 11A and B). We searched for GH family genes in Parhyale using the classification system of the CAZy (Carbohydrate-Active enZYmes) database (Cantarel et al., 2009) and the annotation of protein domains in predicted genes with PFAM (Finn et al., 2006). We identified 73 GH genes with complete GH catalytic domains that were classified into 17 families (Figure 12—source data 1) including 3 members of the GH7 family. Phylogenetic analysis of Parhyale GH7s show high sequence similarity to the known GH7 genes in L. quadripunctata and the amphipod C. terebrans (Kern et al., 2013) (Figure 12A; Figure 12—figure supplement 1). GH7 family genes were also identified in the transcriptomes of three more species spanning the multicrustacea clade: Echinogammarus veneris (amphipod), Eucyclops serrulatus (copepod) and Calanus finmarchicus (copepod). As previously reported, we also discovered a closely related GH7 gene in the branchiopod Daphnia (Figure 12A) (Cragg et al., 2015). This finding supports the grouping of Branchiopoda with Multicrustacea (rather than with Hexapoda) and the acquisition of a GH7 gene by a vericrustacean ancestor. Alternatively, this suggests an even earlier acquisition of a GH7 gene by a crustacean ancestor with subsequent loss of the GH7 family gene in the lineage leading to insects.
GH families 5, 9, 10, and 45 encode beta-1,4-endoglucanases which are also required for lignocellulose digestion and are commonly found across Metazoa. We found 3 GH9 family genes with complete catalytic domains in the Parhyale genome as well as in the other three multicrustacean species (Figure 12B). These GH9 enzymes exhibited a high sequence similarity to their homologues in the isopod Limnoria and in a number of termites. Beta-glucosidases are the third class of enzyme required for digestion of lignocellulose. They have been classified into a number of GH families: 1, 3, 5, 9 and 30, with GH1 representing the largest group (Cantarel et al., 2009). In Parhyale, we found 7 beta-glucosidases from the GH30 family and 3 from the GH9 family, but none from the GH1 family.
Understanding lignocellulose digestion in animals using complex mutualistic interactions with microbes has proven to be a difficult task. The study of 'wood-eating' in Parhyale can offer new insights into lignocellulose digestion in the absence of gut microbes, and the unique opportunity to apply molecular genetic approaches to understand the activity of glycosyl hydrolases in the digestive system. Lignocellulose digestion may also have implications for gut immunity in some crustaceans, since these reactions have been reported to take place in a sterile gut (Boyle and Mitchell, 1978; Zimmer et al., 2002).
Immunity research in Malacostracans has attracted interest due to the rapid rise in aquaculture related problems (Vazquez et al., 2009; Stentiford et al., 2012; Hauton, 2012). Malacostracan food crops represent a huge global industry (>$40 Billion at point of first sale), and reliance on this crop as a source of animal protein is likely to increase in line with human population growth (Stentiford et al., 2012). Here we provide an overview of immune-related genes in Parhyale that were identified by mapping proteins to the ImmunoDB database (Waterhouse et al., 2007). The ability of the innate immune system to identify pathogen-derived molecules is mediated by pattern recognition receptors (PRRs) (Janeway and Medzhitov, 2002). Several groups of invertebrate PRRs have been characterized, i.e. thioester-containing proteins (TEP), Toll-like receptors (TLR), peptidoglycan recognition proteins (PGRP), C-type lectins, galectins, fibrinogen-related proteins (FREP), gram-negative binding proteins (GNBP), Down Syndrome Cell Adhesion Molecules (Dscam) and lipopolysaccharides and beta-1, 3-glucan binding proteins (LGBP).
The functions of PGRPs have been described in detail in insects like D. melanogaster (Werner et al., 2003) and the PGRP family has also been reported in Vertebrates, Molluscs and Echinoderms (Liu et al., 2001; Rehman et al., 2001). Surprisingly, we found no PGRP genes in the Parhyale genome. PGRPs were also not found in other sequence datasets from Branchiopoda, Copepoda and Malacostraca (Figure 13A), raising the possibility of their close phylogenetic relationship (like the GH7 genes). In the absence of PGRPs, the freshwater crayfish Pacifastacus leniusculus relies on a Lysine-type peptidoglycan and serine proteinases, SPH1 and SPH2 that forms a complex with LGBP during immune response (Liu et al., 2011). In Parhyale, we found one LGBP gene and two serine proteinases with high sequence identity to SPH1/2 in Pacifastacus. The D. pulex genome has also an expanded set of Gram-negative binding proteins (proteins similar to LGBP) suggesting a compensatory mechanism for the lost PGRPs (McTaggart et al., 2009). Interestingly, we found a putative PGRP in the Remipede Speleonectes tulumensis (Figure 13A) providing further support for sister group relationship of Remipedia and Hexapoda (von Reumont et al., 2012).
Innate immunity in insects is transduced by three major signaling pathways: the Immune Deficiency (Imd), Toll and Janus kinase/signal transducer and activator of transcription (JAK/STAT) pathways (Dostert et al., 2005; Tanji et al., 2007). We found 16 members of the Toll family in Parhyale including 10 Toll-like receptors (TLRs) (Figure 13B). Some TLRs have been also implicated in embryonic tissue morphogenesis in Parhyale and other arthropods (Benton et al., 2016). Additionally, we identified 7 Imd and 25 JAK/STAT pathway members including two negative regulators: suppressor of cytokine signaling (SOCS), and protein inhibitor of activated STAT (PIAS) (Arbouzova and Zeidler, 2006) (Figure 13—source data 1).
The blood of arthropods (hemolymph) contains hemocyanin which is a copper-binding protein involved in the transport of oxygen, and circulating blood cells called hemocytes for the phagocytosis of pathogens. Phagocytosis by hemocytes is facilitated by the evolutionarily conserved gene family, the thioester-containing proteins (TEPs) (Levashina et al., 2001). Previously sequenced Pancrustacean species contained between 2 to 52 TEPs. We find 5 TEPs in the Parhyale genome. Arthropod hemocyanins themselves are structurally related to phenoloxidases (PO; (Decker and Jaenicke, 2004) and can be converted into POs by conformational changes under specific conditions (Lee et al., 2004). POs are involved in several biological processes (like the melanization immune response, wound healing and cuticle sclerotization) and we identified 7 PO genes in Parhyale. Interestingly, hemocyanins and PO activity have been shown to be highly abundant together with glycosyl hydrolases in the digestive system of Isopods and Amphipods, raising a potential mechanistic link between gut sterility and degradation of lignocellulose (King et al., 2010; Zimmer et al., 2002).
Another well-studied transmembrane protein essential for neuronal wiring and adaptive immune responses in insects is the immunoglobulin (Ig)-superfamily receptor Down syndrome cell adhesion molecule (Dscam) (Schmucker et al., 2000; Watson et al., 2005). Alternative splicing of Dscam transcripts can result in thousands of different isoforms that have a common architecture but have sequence variations encoded by blocks of alternative spliced exons. The D. melanogaster Dscam locus encodes 12 alternative forms of exon 4 (encoding the N-terminal half of Ig2), 48 alternative forms of exon 6 (encoding the N-terminal half of Ig3), 33 alternative forms of exon 9 (encoding Ig7), and 2 alternative forms of exon 17 (encoding transmembrane domains) resulting in a total of 38,016 possible combinations. The Dscam locus in Parhyale (and in other crustaceans analysed) has a similar organization to insects; tandem arrays of multiple exons encode the N-terminal halves of Ig2 (exon 4 array with at least 13 variants) and Ig3 (exon 6 array with at least 20 variants) and the entire Ig7 domain (exon 14 array with at least 13 variants) resulting in at least 3380 possible combinations (Figure 13C–E). The alternative splicing of hypervariable exons in Parhyale was confirmed by sequencing of cDNA clones amplified with Dscam-specific primers. Almost the entire Dscam gene is represented in a single genomic scaffold and exhibits high amino-acid sequence conservation with other crustacean Dscams (Figure 13——figure supplement 1). The number of Dscam isoforms predicted in Parhyale is similar to that predicted for Daphnia species (Brites et al., 2008). It remains an open question whether the higher number of isoforms observed in insects coincides with the evolution of additional Dscam functions compared to crustaceans.
From a functional genomics perspective, the Parhyale immune system appears to be a good representative of the malacostrocan or even multicrustacean clade that can be studied in detail with existing tools and resources.
Non-coding RNAs are a central, but still a relatively poorly understood part of eukaryotic genomes. In animal genomes, different classes of small RNAs are key for genome surveillance, host defense against viruses and parasitic elements in the genome, and regulation of gene expression through transcriptional, post-transcriptional and epigenetic control mechanisms (Castel and Martienssen, 2013; Aravin et al., 2001; Caplen et al., 2001; Brennecke et al., 2007; Gu et al., 2009; Lee et al., 2012; He and Hannon, 2004; Thomson et al., 2006; Filipowicz et al., 2008). The nature of these non-coding RNAs, as well as the proteins involved in their biogenesis and function, can vary between animals. For example, some nematodes have Piwi-interacting short RNAs (piRNAs), while others have replaced these by alternate small RNA based mechanisms to compensate for their loss (Sarkies et al., 2015).
As a first step, we surveyed the Parhyale genome for known conserved protein components of the small interfering RNA (siRNA/RNAi) and the piRNA pathways (Table 4). We found key components of all major small RNA pathways, including 4 argonaute family members, 2 PIWI family members, and orthologs of D. melanogaster Dicer-1 and Dicer-2, drosha and loquacious, (Figure 14—figure supplement 1). Among Argonaute genes, Parhyale has 1 AGO-1 ortholog and 3 AGO-2 orthologs, which is presumably a malacostraca-specific expansion. While Parhyale only has 2 PIWI family members, other crustacean lineages have clearly undergone independent expansions of this protein family. Unlike in C. elegans, many mammals, fish and insects (but not D. melanogaster), we did not find any evidence in the Parhyale genome for the SID-1 (systemic RNA interference defective) transmembrane protein that is essential for systemic RNAi (Dong and Friedrich, 2005;Honeybee Genome Sequencing Consortium, 2006; Xu and Han, 2008). Species without a SID-1 ortholog can silence genes only in a cell-autonomous manner (Roignant et al., 2003). This feature has important implications for future design of RNAi experiments in Parhyale.
We also assessed the miRNA and putative long non-coding RNAs (lncRNA) content of Parhyale using both MiRPara and Rfam (Wu et al., 2011; Nawrocki et al., 2015). We annotated 1405 homologues of known non-coding RNAs using Rfam. This includes 980 predicted tRNAs, 45 rRNA of the large ribosomal subunit, 10 rRNA of the small ribosomal subunit, 175 snRNA components of the major spliceosome (U1, U2, U4, U5 and U6), 5 snRNA components of the minor spliceosome (U11, U12, U4atac and U6atac), 43 ribozymes, 38 snoRNAs, 71 conserved cis-regulatory element derived RNAs and 42 highly conserved miRNA genes (Source code 6). Parhyale long non-coding RNAs (lncRNAs) were identified from the transcriptome using a series of filters to remove coding transcripts producing a list of 220,284 putative lncRNAs (32,223 of which are multi-exonic). Only one Parhyale lncRNA has clear homology to another annotated lncRNA, the sphinx lncRNA from D. melanogaster (Wang et al., 2002).
We then performed a more exhaustive search for miRNAs using MiRPara (Source code 6) and a previously published Parhyale small RNA read dataset (Blythe et al., 2012). We identified 1403 potential miRNA precursors represented by 100 or more reads. Combining MiRPara and Rfam results, we annotated 31 out of the 34 miRNA families found in all Bilateria, 12 miRNAs specific to Protostomia, 4 miRNAs specific to Arthropoda and 5 miRNAs previously found to be specific to Mandibulata (Figure 14). We did not identify mir-125, mir-283 and mir-1993 in the Parhyale genome. The absence of mir-1993 is consistent with reports that this miRNA was lost during Arthropod evolution (Wheeler et al., 2009). While we did not identify mir-125, we observed that mir-100 and let-7 occurred in a cluster on the same scaffold (Figure 14—figure supplement 2), where mir-125 is also present in other animals. The absence of mir-125 has been also reported for the centipede genome (Chipman et al., 2014). mir-100 is one of the most primitive miRNAs shared by Bilateria and Cnidaria (Grimson et al., 2008; Wheeler et al., 2009). The distance between mir-100 and let-7 genes within the cluster can vary substantially between different species. Both genes in Parhyale are localized within a 9.3kb region (Figure 14—figure supplement 2) as compared to 3.8kb in the mosquito Anopheles gambiae and 100bp in the beetle Tribolium (Behura, 2007). Similar to D. melanogaster and the polychaete Platynereis dumerilii, we found that Parhyale mir-100 and let-7 are co-transcribed as a single, polycistronic lncRNA. We also found another cluster with miR-71 and mir-2 family members which is conserved across many invertebrates (Marco et al., 2014) (Figure 14—figure supplement 2).
Conserved linkages have also been observed between miRNAs and Hox genes in Bilateria (Enright et al., 2003a; Tanzer et al., 2005; Lemons and McGinnis, 2006; Stark et al., 2008; Shippy et al., 2008). For example, the phylogenetically conserved mir-10 is present within both vertebrate and invertebrate Hox clusters between Hoxb4/Dfd and Hoxb5/Scr (Enright et al., 2003b). In the Parhyale genome and Hox BAC sequences, we found that mir-10 is also located between Dfd and Src on BAC clone PA179-K23 and scaffold phaw_30.0001203 (Figure 14——figure supplement 2). However, we could not detect mir-iab-4 near the Ubx and AbdA genes in Parhyale, the location where it is found in other arthropods/insects (Cumberledge et al., 1990).
Preliminary evidence regarding the presence of PIWI proteins and other piRNA pathway proteins also suggests that the piRNA pathway is likely active in Parhyale, although piRNAs themselves await to be surveyed. The opportunity to study these piRNA, miRNA and siRNA pathways in a genetically tractable crustacean system will shed further light into the regulation and evolution of these pathways and their contribution to morphological diversity.
Methylation of cytosine residues (m5C) in CpG dinucleotides in animal genomes is regulated by a conserved multi-family group of DNA methyltransferases (DNMTs) with diverse roles in the epigenetic control of gene expression, genome stability and chromosome dynamics (Zemach et al., 2010; Law and Jacobsen, 2010; Jones, 2012). The phylogenetic distribution of DNMTs in Metazoa suggests that the bilaterian ancestor had at least one member of the Dnmt1 and Dnmt3 families (involved in de novo methylation and maintenance of DNA methylation) and the Dnmt2 family (involved in tRNA methylation), as well as additional RNA methyltransferases (Jones and Liang, 2009; Jeltsch et al., 2016). Many animal groups have lost some of these DNA methyltransferases, for example DNMT1 and 3 are absent from D. melanogaster and flatworms (Goll et al., 2006; Jaber-Hijazi et al., 2013), while DNMT2 is absent from nematodes C. elegans and C. briggsae. The Parhyale genome encodes members of all 3 families DNMT1, DNMT3 and DNMT2, as well as 2 orthologs of conserved methyl-CpG-binding proteins and a single orthologue of Tet2, an enzyme involved in DNA demethylation (Hackett et al., 2013) (Figure 15A and Figure 15—source data 1).
We used genome wide bisulfite sequencing to confirm the presence and also assess the distribution of CpG dinucleotide methylation. Our results indicated that 20–30% of Parhyale DNA is methylated at CpG dinucleotides (Figure 15B). The Parhyale methylation pattern is similar to that observed in vertebrates, with high levels of methylation detected in transposable elements and other repetitive elements, in promoters and gene bodies (Figure 15C). A particular class of rolling-circle transposons are very highly methylated in the genome, potentially implicating methylation in silencing these elements. For comparison, about 1% or less of CpG-associated cytosines are methylated in insects like Drosophila, Apis, Bombyx and Tribolium. (Feng et al., 2010; Jeltsch, 2010; Zemach et al., 2010). These data represent the first documentation of a crustacean methylome. Considering the utility of Parhyale for genetic and genomic research, we anticipate future investigations to shed light on the functional importance and spatiotemporal dynamics of epigenetic modifications during normal development and regeneration, as well as their relevance to equivalent processes in vertebrate systems.
Parhyale has already emerged as a powerful model for developmental genetic research where the expression and function of genes can be studied in the context of stereotyped cellular processes and with a single-cell resolution. Several experimental approaches and standardized resources have been established to study coding and non-coding sequences (Table 1). These functional studies will be enhanced by the availability of the assembled and annotated genome presented here. As a first application of these resources, we tested the efficiency of the CRISPR/Cas system for targeted genome editing in Parhyale (Mali et al., 2013; Jinek et al., 2012; Cong et al., 2013; Gilles and Averof, 2014; Martin et al., 2015; Serano et al., 2015). In these studies, we targeted the Distal-less patterning gene (called PhDll-e) (Liubicich et al., 2009) that has a widely-conserved and highly-specific role in animal limb development (Panganiban et al., 1997).
We first genotyped our wild-type laboratory culture and found two PhDll-e alleles with 23 SNPs and 1 indel in their coding sequences and untranslated regions. For PhDll-e knock-out, two sgRNAs targeting both alleles in their coding sequences downstream of the start codon and upstream of the DNA-binding homeodomain were injected individually into 1-cell-stage embryos (G0 generation) together with a transient source of Cas9 (Figure 16—figure supplement 1 A-B). Both sgRNAs gave rise to animals with truncated limbs (Figure 16A and B); the first sgRNA at a relatively low percentage around 9% and the second one at very high frequencies ranging between 53% and 76% (Figure 16—figure supplement 1). Genotyping experiments revealed that injected embryos carried PhDll-e alleles modified at the site targeted by each sgRNA (Figure 16—figure supplement 1B). The number of modified PhDll-e alleles recovered from G0s varied from two, in cases of early bi-allelic editing at the 1-cell-stage, to three or more, in cases of later-stage modifications by Cas9 (Figure 16—figure supplement 1C). We isolated indels of varying length that were either disrupting the open reading frame, likely producing loss-of-function alleles or were introducing in-frame mutations potentially representing functional alleles (Figure 16—figure supplement 1C–D). In one experiment with the most efficient sgRNA, we raised the injected animals to adulthood and set pairwise crosses between 17 fertile G0s (10 male and 7 female): 88% (15/17) of these founders gave rise to G1 offspring with truncated limbs, presumably by transmitting PhDll-e alleles modified by Cas9 in their germlines. We tested this by genotyping individual G1s from two of these crosses and found that embryos bearing truncated limbs were homozygous for loss-of-function alleles with out-of-frame deletions, while their wild-type siblings carried one loss-of-function allele and one functional allele with an in-frame deletion (Figure 16—figure supplement 1 D).
The non-homologous end joining (NHEJ) repair mechanism operating in the injected cells can be exploited not only for gene knock-out experiments described above, but also for CRISPR knock-in approaches where an exogenous DNA molecule is inserted into the targeted locus in a homology-independent manner. This homology-independent approach could be particularly useful for Parhyale that exhibits high levels of heterozygosity and polymorphisms in the targeted laboratory populations, especially in introns and intergenic regions. To this end, we co-injected into 1-cell-stage embryos the Cas9 protein together with the strongest sgRNA and a tagging plasmid. The plasmid was designed in such a way that upon its linearization by the same sgRNA and Cas9 and its integration into the PhDll-e locus in the appropriate orientation and open reading frame, it would restore the endogenous PhDll-e coding sequence in a bicistronic mRNA also expressing a nuclear fluorescent reporter. Among injected G0s, about 7% exhibited a nuclear fluorescence signal in the distal (telopodite and exopodite) parts of developing appendages (Figure 16C and Figure 16—figure supplement 1 E), which are the limb segments that were missing in the knock-out experiments (Figure 16B). Genotyping of one of these embryos demonstrated that the tagged PhDll-e locus was indeed encoding a functional PhDll-e protein with a small in-frame deletion around the targeted region (Figure 16—figure supplement 1 F).
These results, together with the other recent applications of the CRISPR/Cas system to study Hox genes in Parhyale (Martin et al., 2015; Serano et al., 2015), demonstrate that the ability to manipulate the fertilized eggs together with the slow tempo of early cleavages can result in very high targeting frequencies and low levels of mosaicism for both knock-out and knock-in approaches. Considering the usefulness of the genome-wide resources described in this report, we anticipate that the Parhyale embryo will prove an extremely powerful system for fast and reliable G0 screens of gene expression and function.
In this article we described the first complete genome of a malacostracan crustacean species, the genome of the marine amphipod Parhyale hawaiensis. At an estimated size of 3.6 Gb, it is among the largest genomes submitted to NCBI. The Parhyale genome reported here is that of a single adult male from a sib-bred line called Chicago-F. We find Parhyale has an abundance of repetitive sequence and high levels of heterozygosity in the individual sequenced. Combined with analysis of available transcriptome sequences and independently sequenced genomic BAC clones, we conclude high levels of heterozygosity are representative of high levels of single and polynucleotide polymorphisms in the broader laboratory population. Our comparative bioinformatics analyses suggest that the expansion of repetitive sequences and the increase in gene size due to an expansion of intron size have contributed to the large size of the genome. Despite these challenges, the Parhyale genome and associated transcriptomic resources reported here provide a useful assembly of most genic regions in the genome and a comprehensive description of the Parhyale transcriptome and proteome.
Parhyale has emerged since the early 2000’s as an attractive animal model for developmental genetic and molecular cell biology research. It fulfills several desirable biological and technical requirements as an experimental model, including a relatively short life-cycle, year-round breeding under standardized laboratory conditions, availability of thousands of eggs for experimentation on a daily basis, and amenability to various embryological, cellular, molecular genetic and genomic approaches. In addition, Parhyale has stereotyped cell lineages and cell behaviors, a direct mode of development, a remarkable appendage diversity and the capacity to regenerate limbs post-embryonically. These qualities can be utilized to address fundamental long-standing questions in developmental biology, like cell fate specification, nervous system development, organ morphogenesis and regeneration (Stamataki and Pavlopoulos, 2016). Research on these topics will benefit enormously from the standardized genome-wide resources reported here. Forward and reverse genetic analyses using both unbiased screens and candidate gene approaches have already been devised successfully in Parhyale (Table 1). The availability of coding and non-coding sequences for all identified signaling pathway components, transcription factors and various classes of non-coding RNAs will dramatically accelerate the study of the expression and function of genes implicated in the aforementioned processes.
Equally importantly, our analyses highlight additional areas where Parhyale could serve as a new experimental model to address other questions of broad biomedical interest. From a functional genomics perspective, the Parhyale immune system appears to be a good representative of the malacostracan or even the multicrustacean clade that can be studied in detail with existing tools and resources. Besides the evolutionary implications and the characterization of alternative strategies used by arthropods to defend against pathogens, a deeper mechanistic understanding of the Parhyale immune system will be relevant to aquaculture. Some of the greatest setbacks in the crustacean farming industry are caused by severe disease outbreaks. Parhyale is closely related to farmed crustaceans (primarily shrimps, prawns and crayfish) and the knowledge acquired from studying its innate immunity could help enhance the sustainability of this industry by preventing or controlling infectious diseases (Stentiford et al., 2012; Johnson et al., 2008; Lu et al., 2008; Rajesh Kumar et al., 2008; Rowley and Pope, 2012).
An immune-related problem that will be also interesting to explore in Parhyale concerns the possibility of a sterile digestive tract similar to that proposed for limnoriid Isopods (King et al., 2010). Parhyale, like limnoriid Isopods, encodes and expresses all enzymes required for lignocellulose digestion, suggesting that it is able to ’digest wood' by itself without symbiotic microbial partners. Of course, a lot of work still needs to be invested in the characterization of the cellulolytic system in Parhyale before any comparisons can be made with other well-established symbiotic digestion systems of lignocellulose. Nevertheless, the possibility of an experimentally tractable animal model that serves as a living bioreactor to convert lignocellulose into simpler metabolites, suggests that future research in Parhyale may also have a strong biotechnological potential, especially for the production of biofuels from the most abundant and cheapest raw material, plant biomass.
Although more high-quality genomes with a broader phylogenetic coverage are still needed for meaningful evolutionary comparisons, our observations from analysing the Parhyale genome and other crustacean data sets also contribute to the ongoing debate on the relationships between crustacean groups. While the analysis of shared orthologous groups did not provide clear support for either the Allotriocarida hypothesis (uniting Branchiopoda with Hexapoda) or the Vericrustacea hypothesis (uniting Branchiopoda with Malacostraca), we noted the presence of GH7 genes and the absence of PGRP genes in branchiopod and multicrustacean genomes supporting the Vericrustacea hypothesis. It still remains to be proven how reliable these two characters will be to distinguish between these alternative phylogenetic affinities.
Finally, Parhyale was introduced recently as a new model for limb regeneration (Konstantinides and Averof, 2014). In some respects, including the segmented body plan, the presence of a blood system and the contribution of lineage-committed adult stem cells to newly formed tissues, regeneration in Parhyale may resemble the process in vertebrates more than other established invertebrate models (e.g. planarians, hydra). Regenerative research in Parhyale has been founded on transgenic approaches to label specific populations of cells and will be further assisted by the resources presented here. Likewise, we expect that the new genomic information and CRISPR-based genome editing methodologies together with all other facets of Parhyale biology will open other new research avenues not yet imagined.
Raw genomic reads are deposited at NCBI with the project accession: PRJNA306836. All supplemental data including IPython notebook can be downloaded from this figshare link: https://figshare.com/articles/supplemental_data_for_Parhyale_hawaniensis_genome/3498104 Alternatively, the IPython notebooks and associated scripts can also be viewed at the following github repository: https://github.com/damiankao/phaw_genome
About 10 g of genomic DNA were isolated from a single adult male from the Chicago-F isofemale line established in 2001 (Parchem et al., 2010). The animal was starved for one week and treated for 3 days with penicillin-streptomycin (100x, Gibco/Thermo Fisher Scientific), tetracycline hydrochloride (20 g/ml, Sigma-Aldrich) and amphotericin B (200x, Gibco/Thermo Fisher Scientific). It was then flash frozen in liquid nitrogen, homogenized manually with a pestle in a 1.5 ml microtube (Kimble Kontes) in 600 l of Lysis buffer (100 mM Tris-HCl pH 8, 100 mM NaCl, 50 mM EDTA, 0.5% SDS, 200 g/ml Proteinase K, 20 g/ml RNAse A). The lysate was incubated for 3 hr at 37°C, followed by phenol/chloroform extractions and ethanol precipitation. The condensed genomic DNA was fished out with a Pasteur pipette, washed in 70% ethanol, air-dried, resuspended in nuclease-free water and analysed on a Qubit fluorometer (Thermo Fisher Scientific) and on a Bioanalyzer (Agilent Technologies). All genome libraries were prepared from this sample: 1 g of genomic DNA was used to generate the shotgun libraries using the TruSeq DNA Sample Prep kit (Illumina) combined with size-selection on a LabChip XT fractionation system (Caliper Life Sciences Inc) to yield 2 shotgun libraries with average fragment sizes 431 bp and 432 bp, respectively; 4 g of genomic DNA were used to generate 4 mate-pair libraries with average fragment sizes 5.5 kb, 7.3 kb, 9.3 kb and 13.8 kb using the Nextera Mate Pair Sample Preparation kit (Illumina) combined with agarose size selection. All libraries were sequenced on a HiSeq 2500 instrument (Illumina) using paired-end 150 nt reads.
For chromosome spreads, tissue was obtained from embryos at stages 14–18 (Browne et al., 2005). Eggs were taken from the mother and incubated for 1–2 hr in isotonic colchicine solution (0.05% colchicine, artificial sea water). After colchicine incubation, the embryonic tissue was dissected from the egg and placed in hypotonic solution (0.075 M KCl) for 25 min. For tissue fixation, we replaced the hypotonic solution with freshly prepared ice-chilled Carnoy’s fixative (six parts ethanol, three parts methanol and one part anhydrous acetic acid) for 25 min. The fixed tissue was minced with a pair of fine tungsten needles in Carnoy’s solution and the resulting cell suspension was dropped with a siliconized Pasteur pipette from a height of about 5 cm onto a carefully cleaned ice-chilled microscopic slide. After partial evaporation of the Carnoy’s fixative the slides were briefly exposed a few times to hot water vapors to rehydrate the tissue. The slides were then dried on a 75°C metal block in a water bath. Finally, the slides with prepared chromosomes were aged overnight at 60°C. After DNA staining either with Hoechst (H33342, Molecular Probes) or with DAPI (Invitrogen), chromosomes were counted on a Zeiss Axioplan II Imaging equipped with C-Apochromat 63x/1.2 NA objective and a PCO pixelfly camera. FIJI was used to improve image quality (contrast and brightness) and FIJI plugin 'Cell Counter’ was used to determine the number of chromosomes.
The Parhyale raw data and assembled data are available on the NCBI website. Genome assembly was done with Abyss (Simpson et al., 2009) at two different k-mer settings (70, 120) and merged with GAM-NGS. Scaffolding was performed with SSPACE (Boetzer et al., 2011). We chose cut-offs of >95% overlap length and >95% identity when removing shorter allelic contigs before scaffolding as these gave better scaffolding results as assessed by assembly metrics. Transcriptome assembly was performed with Trinity (Haas et al., 2013). The completeness of the genome and transcriptome was assessed by blasting against CEGMA genes (Parra et al., 2007) and visualized by plotting the orthologue hit ratio versus e-value. K-mer analysis of variant and repetitive branching was performed with String Graph Assembler’s preqc module (Simpson, 2014). K-mer intersection analysis was performed using jellyfish2 (Marçais and Kingsford, 2011). Repetitive elements were annotated with RepeatModeler and RepeatMasker. An in-depth description of the assembly process and repeat masking is detailed in source code 1 and 2.
Parhyale transcriptome assembly was generated from Illumina reads collected from diverse embryonic stages (Stages 19, 20, 22, 23, 25, and 28), and adult thoracic limbs and regenerating thoracic limbs (3 and 6 days post amputation). For the embryonic samples, RNA was extracted using Trizol; PolyA+ libraries were prepared with the Truseq V1 kit (Illumina), starting with 0.6–3.5 μg of total mRNA, and sequenced on the Illumina Hiseq 2000 as paired-end 100 base reads, at the QB3 Vincent J. Coates Genomics Sequencing Laboratory. For the limb samples, RNA was extracted using Trizol; PolyA+ libraries were prepared with the Truseq V2 kit (Illumina), starting with 1 μg of total mRNA, and sequenced on the Illumina Hiseq 2500 as paired-end 100 base reads, at the IGBMC Microarray and Sequencing platform. 260 million reads from embryos and 180 million reads from limbs were used for the transcriptome assembly. Prior to the assembly we trimmed adapter and index sequences using cutadapt (Martin, 2011). We also removed spliced leader sequences: GAATTTTCACTGTTCCCTTTACCACGTTTTACTG, TTACCAATCACCCCTTTACCAAGCGTTTACTG, CCCTTTACCAACTCTTAACTG, CCCTTTACCAACTTTACTG using cutadapt with 0.2 error allowance to remove all potential variants (Douris et al., 2009). To assemble the transcriptome we used Trinity (version trinityrnaseq_r20140413) (Haas et al., 2013) with settings: -min_kmer_cov 2, -path_reinforcement_distance 50.
Gene prediction was done with a combination of Evidence Modeler (Haas et al., 2008) and Augustus (Stanke and Waack, 2003). The transcriptome was first mapped to the genome using GMAP (Wu and Watanabe, 2005). A secondary transcriptome reference assembly was performed with STAR/Cufflinks (Trapnell et al., 2010; Dobin et al., 2013). The transcriptome mapping and Cufflinks assembly was processed through the PASA pipeline (Haas et al., 2008) to consolidate the annotations. The PASA dataset, a set of Exonerate (Slater and Birney, 2005) mapped Uniprot proteins, and Ab inito GeneMark (Lukashin and Borodovsky, 1998) predictions were consolidated with Evidence Modeler to produce a set of gene annotations. A high confidence set of gene models from Evidence Modeler containing evidence from all three sources was used to train Augustus. Evidence from RepeatMasker (Smit et al., 2013, PASA and Exonerate were then used to generate Augustus gene predictions. A final list of genes for down-stream analysis was generated using both transcriptome and gene predictions (canonical proteome dataset). Detailed methods are described in Source code 3.
For variant analysis on the BAC clones, the short shot-gun library genomic reads were mapped to the BAC clones individually. GATK was then used to call variants. For variant analysis on the genic regions, transcript sequences used to generate the canonical proteome dataset were first aligned to the genome assembly. Genome alignments of less than 30 base pairs were discarded. The possible genome alignments were sorted based on number of mismatches with the top alignment having the least amount of mismatches. For each transcript, the top two genome aligments were used to call potential variants. Trascripts or parts of transcripts where there were more than five genomic mapping loci were discarded as potentially highly conserved domains or repetitive regions. Detailed methods of this process are described in Source code 4.
Parhyale genes (nucleotide sequences) were downloaded from GenBank. Each gene was used as a query for blastn against the Parhyale genome using the Geneious software (Kearse et al., 2012). In each case two reference contig hits were observed where both had E values of close to zero. A new sequence called geneX_snp was created and this sequence was annotated with the snps and/or indels present in the alternative genomic contigs. To determine the occurrence of synonymous and non-synonymous substitutions, the original query and the newly created sequence (with polymorphisms annotated) were in silico translated into protein sequences followed by pairwise alignment. Regions showing amino acid changes were annotated as non-synonymous substitutions. Five random genes from the catalogue were selected for PCR, cloning and Sanger sequencing to confirm genomic polymorphisms and assess further polymorphism in the lab popultaion. Primers for genomic PCR designed to capture and amplify exon regions are listed as the following: dachshund (PH1F = 5’- GGTGCGCTAAATTGAAGAAATTACG-3’ and PH1R = 5’- ACTCAGAGGGTAATAGTAACAGAA-3’), distalless exon 2 (PH2F = 5’-CACGGCCCGGCACTAACTATCTC-3’ and PH2R = 5’-GTAATATATCTTACAACAACGACTGAC-3’), distalless exon 3 (PH3F = 5’-GGTGAACGGGCCGGAGTCTC-3’ and PH3R = 5’-GCTGTGGGTGCTGTGGGT-3’), homothorax (PH4F = 5’-TCGGGGTGTAAAAAGGACTCTG-3’ and PH4R = 5’-AACATAGGAACTCACCTGGTGC-3’), orthodenticle (PH5F = 5’-TTTGCCACTAACACATATTTCGAAA-3’ and PH5R = 5’-TCCCAAGTAGATGATCCCTGGAT-3’) and prospero (PH6F = 5’-TACACTGCAACATCCGATGACTTA-3’ and PH6R = 5’-CGTGTTATGTTCTCTCGTGGCTTC-3’).
Evolutionary analyses and comparative genomics were performed with 16 species: D. melanogaster, A. gambiae, D. pulex, L. salmonis, S.maritima, S. mimosarum, M. martensii, I. scapularis, H. dujardini, C. elegans, B. malayi, T. spiralis, M. musculus, H. sapiens, and B. floridae. For orthologous group analyses, gene families were identified using OrthoFinder (Emms and Kelly, 2015). The canonical proteome was used as a query in BlastP against proteomes from 16 species to generate a distance matrix for OrthoFinder to normalize and then cluster with MCL. Detailed methods are described in Source code 5. For the comparative BLAST analysis, five additional transcriptome datasets were used from the following crustacean species: Litopenaeus vannamei, Echinogammarus veneris, Eucyclops serrulatus, Calanus finmarchicus, Speleonectes tulumensis.
Embryo fixation and in-situ hybridization was performed according to (Rehm et al., 2009). To enhance the nascent nuclear signal over mature cytoplasmic transcript, we used either early germband embryos (Stages 11 – 15) in which expression of lab, Dfd, and Scr are just starting (Serano et al., 2015), or probes that contain almost exclusively intron sequence (Ubx, abd-A, Abd-B, and en1). Lab, Dfd, and Scr probes are described in (Serano et al., 2015). Template for the intron-spanning probes were amplified using the following primers: en1-Intron1, AAGACACGACGAGCATCCTG and CTGTGTATGGCTACCCGTCC; Ubx-Intron1, GGTATGACAGCCGTCCAACA and AGAGTGCCAAGGATACCCGA; abd-A, CGATATACCCAGTCCGGTGC and TCATCAGCGAGGGCACAATT; Abd-B, GCTGCAGGATATCCACACGA and TGCAGTTGCCGCCATAGTAA.
A T7-adapter was appended to the 5’ end of each reverse primer to enable direct transcription from PCR product. Probes were labeled with either Digoxigenin (DIG) or Dinitrophenol (DNP) conjugated UTPs, and visualized using sheep -DIG (Roche) and donkey -Sheep AlexaFluor 555 (Thermo Fischer Scientific), or Rabbit -DNP (Thermo Fischer Scientific) and Donkey -Rabbit AlexaFluor 488 (Jackson ImmunoResearch), respectively. Preparations were imaged on an LSM 780 scanning laser confocal (Zeiss), and processed using Volocity software (Perkin-Elmer).
The identification of GH family genes was done by obtaining Pfam annotations (Finn et al., 2006) for the Parhyale canonical proteome. Pfam domains were classified into different GH families based on the CAZy database (Cantarel et al., 2009). For immune-related genes, best-reciprocal blast was performed with ImmunoDB genes (Waterhouse et al., 2007).
Multiple sequence alignments of protein sequences for gene families of FGF, FGFR, CERS, GH7, GH9, PGRP, Toll-like receptors, DICER, Piwi and Argonaute were performed using MUSCLE (Edgar, 2004). Phylogenetic tree construction was performed with RAxML (Stamatakis, 2014) using the WAG+G model from MUSCLE multiple alignments.
Libraries for DNA methylation analysis by bisulfite sequencing were constructed from 100ng of genomic DNA extracted from one Parhyale male individual, using the Illumina Truseq DNA methylation kit according to manufacturers instructions. Alignments to the Parhyale genome were generated using the core Bismark module from the program Bismark (Krueger and Andrews, 2011), having first artificially joined the Parhyale contigs to generate 10 pseudo-contigs as the program is limited as to the number of separate contigs it can analyse. We then generated genome-wide cytosine coverage maps using the bismark_methylation_extraction module with the parameter 'CX specified to generate annotations of CG, CHH and CHG sites. In order to analyse genome-wide methylation patterns only cytosines with more than a 10 read depth of coverage were selected. Overall methylation levels at CG, CHH and CHG sites were generated using a custom Perl script. To analyse which regions were methylated we mapped back from the joined contigs to the original contigs and assigned these to functional regions based on RepeatMasker (Smit et al., 2013) and transcript annotations of repeats and genes respectively. To generate overall plots of methylation levels in different features we averaged over all sites mapping to particular features, focusing on CG methylation and measuring the% methylation at each site as the number of reads showing methylation divided by the total number of reads covering the site. Meta gene plots over particular features were generated similarly except that sites mapping within a series of 100 bp wide bins from 1000 bp upstream of the feature start site and onward were collated.
For the identification of Dscam in the Parhyale, we used the Dscam protein sequence from crustaceans D. pulex (Brites et al., 2008 ) and L. vannamei (Chou et al., 2009-12) as queries to probe the assembled genome using tBlastN. A 300kb region on scaffold phaw_30.0003392 was found corresponding to the Parhyale Dscam extending from IG1 to FN6 exons. This sequence was annotated using transcriptome data together with manual searches for open reading frames to identify IG, FN exons and exon-intron boundaries (Figure 13—supplemental figure 1). Hypervariable regions of IG2, IG3 and IG7 were also annotated accordingly on the scaffold (Figure 13—supplemental figure 1). This region represents a bona fide Dscam paralog as it matches the canonical extracellular Dscam domain structure of nine IGs – four FNs – one IG and two FNs. Parhyale mRNA extractions were performed using the Zymo Research Direct-zol RNA MiniPrep kit according to manufacturer’s instructions. Total RNA extract was used for cDNA synthesis using the Qiagen QuantiTect Reverse Transcription Kit according to manufacturer’s instructions. To identify and confirm potential hypervariable regions from the Parhyale (Ph-Dscam) transcript, three regions of Ph-Dscam corresponding to IG2, IG3 and IG7 exons respectively were amplified using the following primer pairs. IG2 region:
DF1 = 5’-CCCTCGTGTTCCCGCCCTTCAAC-3’
DR1 = 5’-GCGATGTGCAGCTCTCCAGAGGG-3’
DF2 = 5’-TCTGGAGAGCTGCACATCGCTAAT-3’
DR2 = 5’-GTGGTCATTGCGTACGAAGCACTG-3’
DF3 = 5’-CGGATACCCCATCGACTCCATCG-3’
DR3 = 5’-GAAGCCGTCAGCCTTGCATTCAA-3’
PCR of each region was performed using Phusion High-fidelity polymerase from Thermo Fisher Scientific and thermal cycling was done as the following: 98C 30s, followed by 30 cycles of 98C 10s, 67C 30s, 72C 1m30s, and then 72C 5m. PCR products were cloned into pGEMT-Easy vector and a total of 81 clones were selected and Sanger sequenced and in silico translated in the correct reading frame using Geneious (R7; (Kearse et al., 2012) for multiple sequence alignment.
Parhyale non-protein-coding RNAs were identified using two independent approaches. Infernal 1.1.1 (Nawrocki and Eddy, 2013) was used with the RFAM 12.0 database (Nawrocki et al., 2015) to scan the genome to identify potential non-coding RNAs. Additionally, MiRPara (Wu et al., 2011) was used to scan the genome for potential miRNA precursors. These potential precursors were further filtered using small RNA read mapping and miRBase mapping (Griffiths-Jones et al., 2008). Putative lncRNAs were identified from the transcriptome by applying filtering criteria including removal of known and predicted coding RNAs. Detailed methods are available in Supplementary Data 11.
To genotype our wild-type population, extraction of total RNA and preparation of cDNA from embryos were carried out as previously described (Pavlopoulos et al., 2009). The PhDll-e cDNA was amplified with primers PhDlle_2For (5’-TTTGTCAGGGATCTGCCATT-3’) and PhDlle_1852Rev (5’-TAGCGGCTGACGGTTGTTAC-3’), purified with the DNA Clean and Concentrator kit (Zymo Research), cloned with the Zero Blunt TOPO PCR Cloning Kit (Thermo Fisher Scientific) and sequenced with primers M13 forward (5’- GTAAAACGACGGCCAG-3’) and M13 reverse (5’- CAGGAAACAGCTATGAC-3’).
Each template for sgRNA synthesis was prepared by annealing and PCR amplification of the sgRNA-specific forward primer Dll1: (18 nt PhDll-e-targeted sequence underlined)
or Dll2: (20 nt PhDll-e-targeted sequence underlined)
together with the universal reverse primer:
using the Phusion DNA polymerase (New England Biolabs).
Each PCR product was gel-purified with the Zymoclean DNA recovery kit (Zymo Research) and 150 ng of DNA were used as template in an in vitro transcription reaction with the Megashortscript T7 kit (Thermo Fisher Scientific). A 4-hr incubation at 37°C was followed by DNAse digestion, phenol/chloroform extraction, ethanol precipitation and storage in ethanol at −20° C according to the manufacturer’s instructions. Before microinjection, a small aliquot of the sgRNA was centrifuged, the pellet was washed with 70% ethanol, resuspended in nuclease-free water and quantified on a Nanodrop spectrophotometer (Thermo Scientific). The Cas9 was provided either as in vitro synthesized caped mRNA or as recombinant protein. Cas9 mRNA synthesis was carried out as previously described (Kontarakis and Pavlopoulos, 2014) using plasmid T7-Cas9 (a gift from David Stern and Justin Crocker) linearized with EcoRI digestion. The lyophilized Cas9 protein (PNA Bio Inc) was resuspended in nuclease-free water at a concentration of 1.25 g/l and small aliquots were stored at −80°C. For microinjections, we mixed 400 ng/l of Cas9 protein with 40–20040-200 ng/l sgRNA, incubated at 37°C for 5 min, transferred on ice, added the inert dye phenol red (5x from Sigma-Aldrich) and, for knock-in experiments, the tagging plasmid at a concentration of 10 ng/l. The injection mix was centrifuged for 20 min at 4°C and the cleared solution was microinjected into 1-cell-stage embryos as previously described (Kontarakis and Pavlopoulos, 2014).
In the knock-out experiments, embryos were scored for phenotypes under a bright-field stereomicroscope 7–8 days after injection (stage S25-S27) when organogenesis is almost complete and the limbs are clearly visible through the transparent egg shell. To image the cuticle, anaesthetized hatchlings were fixed in 2% paraformaldehyde in 1xPBS for 24 hr at room temperature. The samples were then washed in PTx (1xPBS containing 1% TritonX-100) and stained with 1 mg/ml Congo Red (Sigma-Aldrich) in PTx at room temperature with agitation for 24 hr. Stained samples were washed in PTx and mounted in 70% glycerol for imaging. Serial optical sections were obtained at 2 m intervals with the 562 nm laser line on a Zeiss 710 confocal microscope using the Plan-Apochromat 10x/0.45 NA objective. Images were processed with Fiji (http://fiji.sc) and Photoshop (Adobe Systems Inc).
This methodology enabled us to also extract genomic DNA for genotyping from the same imaged specimen. Each specimen was disrupted with a disposable pestle in a 1.5 ml microtube (Kimble Kontes) in 50 l of Squishing buffer (10 mM Tris-HCl pH 8, 1 mM EDTA, 25 mM NaCl, 200 g/ml Proteinase K). The lysate was incubated at 37°C for a minimum of 2 hr, followed by heat inactivation of the Proteinase K for 5 min at 95°C, centrifugation at full speed for 5 min and transferring of the cleared lysate to a new tube. To recover the sequences in the PhDll-e locus targeted by the Dll1 and Dll2 sgRNAs, 5 µl of the lysate were used as template in a 50 µl PCR reaction with the Phusion DNA polymerase (New England Biolabs) and primers 313For (5’-TGGTTTTAGCAACAGTGAAGTGA-3’) and 557Rev (5’-GACTGGGAGCGTGAGGGTA-3’). The amplified products were purified with the DNA Clean and Concentrator kit (Zymo Research), cloned with the Zero Blunt TOPO PCR Cloning Kit (Thermo Fisher Scientific) and sequenced with the M13 forward primer.
For the knock-in experiments, we constructed the tagging plasmid pCRISPR-NHEJ-KI-Dll-T2A-H2B-Ruby2 that contained the PhDll-e coding sequence fused in-frame with the T2A self-cleaving peptide, the Parhyale histone H2B and the Ruby 2 monomeric red fluorescent protein, followed by the PhDll-e 3’UTR and the pGEM-T Easy vector backbone (Promega). This tagging plasmid has a modular design with unique restriction sites for easy exchange of any desired part. More details are available upon request. Embryos co-injected with the Cas9 protein, the Dll2 sgRNA and the pCRISPR-NHEJ-KI-Dll-T2A-H2B-Ruby2 tagging plasmid were screened for nuclear fluorescence in the developing appendages under an Olympus MVX10 epi-fluorescence stereomicroscope. To image expression, live embryos at stage S22 were mounted in 0.5% SeaPlaque low-melting agarose (Lonza) in glass bottom microwell dishes (MatTek Corporation) and scanned as described above acquiring both the fluorescence and transmitted light on an inverted Zeiss 880 confocal microscope. To recover the chromosome-plasmid junctions, genomic DNA was extracted from transgenic siblings with fluorescent limbs and used as template in PCR reaction as described above with primer pair 313For and H2BRev (5’-TTACTTAGAAGAAGTGTACTTTG-3’) for the left junction and primer pair M13 forward and 557Rev for the right junction. Amplified products were purified and cloned as described above and sequenced with the M13 forward and M13 reverse primers.
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K VijayRaghavanReviewing Editor; Tata Institute for Fundamental Research, India
In the interests of transparency, eLife includes the editorial decision letter and accompanying author responses. A lightly edited version of the letter sent to the authors after peer review is shown, indicating the most substantive concerns; minor comments are not usually included.
Thank you for submitting your article "The genome of Parhyale hawaiensis: a model for animal development, regeneration, immunity and ligno-cellulose digestion" for consideration by eLife. Your article has been reviewed by three peer reviewers, including Heinrich Reichert (Reviewer #2), and the evaluation has been overseen by K VijayRaghavan as the Reviewing Editor and Senior Editor.
The reviewers have discussed the reviews with one another and the Reviewing Editor has drafted this decision to help you prepare a revised submission.
For long, our understanding of biology has advanced through studies in 'model' organisms that rode wave of the molecular revolution. Recent advances in imaging and genome editing hold a similar promise for other organisms that offer great potential for fundamental discoveries in cellular and developmental biology and an understanding of biology more representative of the diversity of life on Earth.
Within the last two decades, the crustacean Parhyale hawaiensis, has emerged as one such new model organism, particularly for studying limb development and postembryonic limb regeneration. This is due to favorable technical and biological features such as short life cycle, year round breeding in the lab and the production of large numbers of eggs for in vivo experimentation. However, in contrast to the other leading crustacean model, the water flea Daphnia, a complete genome sequence and corresponding annotation are lacking in Parhyale, and this lack is currently a major stumbling block for rapid experimental progress in this malacostracan system. In this light, its genome, described in this paper, has been an eagerly awaited resource.
In this paper, the authors have sequenced, analysed and annotated the genome of Parhyale hawaiensis, which belongs to the malacostracan clade of pancrustaceans. Significantly, it is among the first few non-hexapod genomes to be sequenced, which, given the vast diversity of the arthropods needs to be explored further. Important features of this genome include:
• Its large size. At 3.6GB, is also among the largest genomes to be sequenced.
• Presence of repetitive sequences (including transposable elements), which contributes to the large genome size.
• High levels of heterozygosity.
• Presence of enzymes for lignocellulose digestion.
• Presence of a wide repertoire of genes related to innate immunity.
• Presence of non-coding RNAs and pathways that process them.
• Significant levels of methylation, especially at the sites of transposable elements suggesting epigenetic silencing of regions of the genome.
Importantly, the Parhyale hawaiensis genome will be an invaluable resource for functional genomic studies in a crustacean species that has otherwise already been established as a model laboratory organism. The authors demonstrate the power of this by using the CRISPR/Cas9 technology to knock-out the function of, as well as knock-in a tag into the distalless gene, which is involved in limb development.
The high level of heterozygosity in the genome is particularly striking. Does the use of an isogenised line affect the assessment of this heterozygosity? Does the high heterozygosity in turn affect the methods of sequencing/assembly, and if so, do special techniques have to be employed for these processes? For example, the authors show that regions of high coverage show low heterozygosity whereas regions of low coverage show high levels of heterozygosity. However, data from transcriptome analysis finds no such differences heterozygosity between these groups. While the authors see this as an attribute of read coverage in divergent regions, could the inverse be true? Could the assessment of heterozygosity be exaggerated due to lower coverage? We are sure the authors have considered these possibilities, and it might be helpful if they were discussed in the paper for the broad audience of eLife readership.
While the Introduction seems to suggest that this genome will help solve the disputed phylogeny of the pan crustaceans, in fact the phylogeny is still ambiguous, we presume because high quality genome data does not exist for other members. (In the Discussion, however, the authors favour one hypothesis.) It might be valuable if the authors instead stated explicitly that this data is not sufficient to sort out the phylogeny and more genomes need to be sequenced to work it out.
This paper is written from a functional genomics perspective and in general we think the authors shy away from making definitive statements/discussing their findings from an evolutionary perspective. For example, the authors do perform a comparative analysis with proteomes. However, when they discuss individual protein families, they don't comment on the evolutionary ramifications, except for a few cases (GH7 and PGRPs). While we understand that often no evolutionary conclusions might be possible, leaving the matter unaddressed makes the writing feel like it's very much on the backfoot and leaves the reader expecting a discussion that never came!https://doi.org/10.7554/eLife.20062.056
[…] Specific comments:
The high level of heterozygosity in the genome is particularly striking. Does the use of an isogenised line affect the assessment of this heterozygosity?
In this study, we sequenced a single adult male specimen from a line (called Chicago-F) derived from a single female after two rounds of sib mating. Specifically, F1 offspring from a single female were interbred, and from this collection of siblings a single gravid female was removed and its F2 offspring in turn interbred. A single F2 gravid female was then selected and from this single brood the Chicago-F line was established.
We have added the following text to clarify this:
“Sequencing was performed on genomic DNA isolated from a single adult male taken from a line derived from a single female and expanded after two rounds sib-mating”.
This level of inbreeding will not greatly reduce levels of starting heterozygosity, but equally the sequence of one individual alone tell us a little about population level polymorphism. Our primary goal was the de novo assembly of the very complex Parhyale genome, rather than the assessment of population genetic parameters. Nevertheless, in order to get a better view of polymorphism levels in our laboratory populations, we also analysed genomic data in comparison to previously sequenced BAC clones from the same Chicago-F strain, and transcriptomic data and targeted Sanger sequencing from the broader lab population. These analyses are described in the section “High levels of heterozygosity and polymorphism in the Parhyale genome”.
Does the high heterozygosity in turn affect the methods of sequencing/assembly, and if so, do special techniques have to be employed for these processes?
In order to clarify our approach we have added text and the following citation:
“Different strategies have been employed to sequence highly heterozygous diploid genomes of non-model and wild-type samples (Kajitani R. et al., Efficient de novo assembly of highly heterozygous genomes from whole-genome shotgun short reads, Genome Research 24:1384–1395).”
We have also slightly rewritten the description of our assembly process to be more accessible in the current version:
“We aimed for an assembly representative of different haplotypes, allowing manipulations to be targeted to different allelic variants in the assembly. […] We then kept the longer contig of each pair for scaffolding using our mate-pair libraries (Figure 3F), after which we added back the shorter allelic contigs to produce the final genome assembly (Figure 4A).”
For example, the authors show that regions of high coverage show low heterozygosity whereas regions of low coverage show high levels of heterozygosity. However, data from transcriptome analysis finds no such differences heterozygosity between these groups. While the authors see this as an attribute of read coverage in divergent regions, could the inverse be true? Could the assessment of heterozygosity be exaggerated due to lower coverage? We are sure the authors have considered these possibilities, and it might be helpful if they were discussed in the paper for the broad audience of eLife readership.
To clarify, regions of the genome with higher heterozygosity between alleles assemble as separate contigs and regions with lower heterozygosity between alleles as a single contig. The actual distribution of heterozygosity is a continuous variable but the nature of both the assembly and mapping algorithms separates regions of higher and lower heterozygosity. Genome wide heterozygosity is considered in two places in our work, during k-mer analysis before assembly and during our scaffolding process. To make things clearer, in addition to the edits above, we have edited the text as follows:
“The k-mer analysis revealed a bimodal distribution of error-free k-mers (Figure 3A). The higher-frequency peak corresponded to k-mers present on both haplotypes (i.e. homozygous regions), while the lower-frequency peak had half the coverage and corresponded to k-mers present on one haplotype (i.e. heterozygous regions) (Simpson and Durbin, 2011). We concluded that the single sequenced adult Parhyale exhibits very high levels of heterozygosity, similar to the highly heterozygous oyster genome (see below)."
We then turn our attention from the whole assembly to gene loci (transcribed regions) identified on the assembled contigs. In remapping genomic reads to these regions we found that, not surprisingly, genes with lower heterozygosity had higher number of mapped reads (150x). This is because reads from both haplotypes in the sequenced individual can map to these genes. Conversely for genes with higher heterozygosity only reads from the same haplotype map, and hence they have approximately half the coverage (75x). This of course is very similar to the assembly process and k-mer analysis presented earlier. To clarify our method and explain our findings we have rewritten the text as follows:
“To estimate the level of heterozygosity in genes we first identified transcribed regions of the genome by mapping back transcripts in the assembly. […] Thus, we conclude that heterozygosity influences read mapping and assembly of transcribed regions, and not just non-coding parts of the assembly”
Similarly we have rewritten the text concerning analysis of polymorphism in transcribed regions amongst the wider laboratory population so it explains our findings with greater clarity:
“The assembled Parhyale transcriptome was derived from various laboratory populations, hence we expected to see additional polymorphisms beyond those detected in the two haplotypes of the individual male we sequenced. […] For example, we found that the cDNAs of the germ line determinants, nanos (78 SNPS, 34 non-synonymous substitutions and one 6bp indel) and vasa (37 SNPs, 7 non-synonymous substitutions and one 6bp indel) can have more variability within laboratory Parhyale populations than might be observed for orthologs between closely related species.”
While the Introduction seems to suggest that this genome will help solve the disputed phylogeny of the pan crustaceans, in fact the phylogeny is still ambiguous, we presume because high quality genome data does not exist for other members. (In the Discussion, however, the authors favour one hypothesis.) It might be valuable if the authors instead stated explicitly that this data is not sufficient to sort out the phylogeny and more genomes need to be sequenced to work it out.
This paper is written from a functional genomics perspective and in general we think the authors shy away from making definitive statements/discussing their findings from an evolutionary perspective. For example, the authors do perform a comparative analysis with proteomes. However, when they discuss individual protein families, they don't comment on the evolutionary ramifications, except for a few cases (GH7 and PGRPs). While we understand that often no evolutionary conclusions might be possible, leaving the matter unaddressed makes the writing feel like it's very much on the backfoot and leaves the reader expecting a discussion that never came!
We agree that the paucity of high-quality assembled genomes from the non-hexapod pancrustacean lineages does not allow any final conclusions to be drawn regarding their phylogenetic relationships. Although, we present certain similarities between Branchiopoda and Malacostraca in terms of gene gain/loss, currently we do not favour either the Allotriocarida or Vericrustacea hypothesis. Therefore, we have modified the text in the Introduction as follows:
“The genome of the amphipod crustacean Parhyale hawaiensis addresses the paucity of high quality non-hexapod genomes among the pancrustacean group, and will help to resolve relationships within this group as more genomes and complete proteomes become available (Rivarola-Duarte et al., 2014, Kenny et al., 2014).”
From the immunity Results section we have deleted the lines:
“Interestingly, the loss of PGRPs and presence of GH7 genes in Branchiopoda, similar to the presence of GH7 genes, supports their close relationship with the Multicrustacea rather than the Hexapoda.”
In the Discussion we have modified text as follows:
“Although more high-quality genomes with a broader phylogenetic coverage are still needed for meaningful evolutionary comparisons, our observations from analysing the Parhyale genome and other crustacean data sets also contribute to the ongoing debate on the relationships between crustacean groups. […] It still remains to be proven how reliable these two characters will be to distinguish between these alternative phylogenetic affinities.”
We hope this is a more accurate reflection of our expectations and findings and improves the accessibility of the manuscript.https://doi.org/10.7554/eLife.20062.057
- Damian Kao
- Alvina G Lai
- Alessia Di Donfrancesco
- Natalia Pouchkina-Stancheva
- Aziz Aboobaker
- Damian Kao
- Alvina G Lai
- Alessia Di Donfrancesco
- Natalia Pouchkina-Stancheva
- Aziz Aboobaker
- Alvina G Lai
- Alvina G Lai
- Aziz Aboobaker
- Evangelia Stamataki
- Suyash Kumar
- Igor Siwanowicz
- Andy Le
- Andrew Lemire
- Michael B Eisen
- Silvana Rosic
- Peter Sarkies
- Nikolaos Konstantinides
- Marie Semon
- Marco Grillo
- Michalis Averof
- Erin Jarvis
- Heather Bruce
- Nipam H Patel
- Peter Sarkies
- Aziz Aboobaker
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
We are grateful to Serge Picard for sequencing the genome libraries, and Frantisek Marec and Peer Martin for useful advice on Parhyale karyotyping.
- K VijayRaghavan, Tata Institute for Fundamental Research, India
© 2016, Kao et al.
This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.
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