Meiotic drivers are selfish genes that bias their transmission into gametes, defying Mendelian inheritance. Despite the significant impact of these genomic parasites on evolution and infertility, few meiotic drive loci have been identified or mechanistically characterized. Here, we demonstrate a complex landscape of meiotic drive genes on chromosome 3 of the fission yeasts Schizosaccharomyces kambucha and S. pombe. We identify S. kambucha wtf4 as one of these genes that acts to kill gametes (known as spores in yeast) that do not inherit the gene from heterozygotes. wtf4 utilizes dual, overlapping transcripts to encode both a gamete-killing poison and an antidote to the poison. To enact drive, all gametes are poisoned, whereas only those that inherit wtf4 are rescued by the antidote. Our work suggests that the wtf multigene family proliferated due to meiotic drive and highlights the power of selfish genes to shape genomes, even while imposing tremendous costs to fertility.https://doi.org/10.7554/eLife.26033.001
Animals, plants and fungi produce sex cells – known as gametes – when they are preparing to reproduce. These cells are made when cells containing two copies of every gene in the organism divide to produce new cells that each only have one copy of each gene. Therefore, a particular gene copy usually has a 50% chance of being carried by each gamete. There is a group of genes that selfishly increase their chances of being transmitted to the next generation by destroying the gametes that do not carry them. These “gamete killer” genes can lead to infertility and other health problems.
Fission yeast is a fungus that is widely used in research. Previous studies revealed that the yeast are likely to have several gamete killers, but the identities of these genes or how they work were not clear. Nuckolls, Bravo Núñez et al. sought to identify at least one gamete killer gene and understand how it works.
The experiments found that a gene called wtf4 acts as a gamete killer in fission yeast. This gene encodes two different proteins, one that acts as a poison and one that acts as an antidote. The antidote remains inside the gametes that contain the wtf4 gene, while the poison is released in the surrounding environment. The poison is capable of killing all of the gametes, but the antidote protects the gametes that contain the wtf4 gene. Further experiments show that wtf4 is just one member of a large family of genes that are also likely to play roles in selectively killing gametes.
A separate study by Hu et al. found that two other members of the wtf family also act as gamete killers in fission yeast. Together, these findings expand our understanding of the nature of gamete killers and how they can contribute to infertility. This may guide the search for gamete killers in humans and other organisms. In the future, gamete killers could potentially be used to eradicate populations of pests that damage crops or spread diseases in humans.https://doi.org/10.7554/eLife.26033.002
Infertility can be perplexingly high within eukaryotic species. For example, more than one out of every seven human couples are infertile (Thoma et al., 2013). This high infertility is at odds with the fundamental requirement of reproductive success for Darwinian fitness. A potential solution to this infertility paradox is the presence of selfish genes that subvert meiosis to increase their transmission into gametes (Ségurel et al., 2011; Presgraves, 2010; Johnson, 2010); such selfish genes might explain a subset of cases of human infertility. Gamete-killing meiotic drive alleles are one such class of selfish genes that can directly cause infertility. These genes act by killing the gametes that do not inherit them, increasing their transmission into up to 100% of the progeny of a heterozygote (Lindholm et al., 2016; Sandler and Novitski, 1957). Meiotic drivers can also indirectly result in infertility or other disease states by interfering with natural selection’s ability to choose the most well-adapted alleles. Natural selection cannot harness the fitness benefits of alleles carried in gametes destroyed by drive. Furthermore, meiotic drivers can promote the spread of maladapted alleles that are genetically linked to the drive locus within a population (Sandler and Novitski, 1957; Crow, 1991). Because drive can be harmful to the overall fitness of a species, suppressors of drive often evolve in response (Crow, 1991).
Gamete-killing meiotic drive has been observed in eukaryotes ranging from plants to mammals (Lindholm et al., 2016). With the broadening implementation of high-throughput sequencing of both meiotic products and cross progeny to measure allele transmission, the presence of meiotic drive is being observed at an accelerated rate, and it is hypothesized that these selfish genes are common (Lindholm et al., 2016; Didion et al., 2015; Ottolini et al., 2015; Grognet et al., 2014; Burt and Trivers, 2006). However, only a handful of genes involved in meiotic drive have been identified. Lack of homology among these genes makes it nearly impossible to identify novel drive loci from genome sequences alone. Instead, rigorous genetic analyses are required to detect and map meiotic drive loci. These efforts are frequently impeded by the complexity of many drive systems; they often have multiple components and are found within chromosome rearrangements that are recalcitrant to genetic mapping (Larracuente and Presgraves, 2012; Bauer et al., 2012). Even in the case of well-studied meiotic drive systems where one or more components have been identified, a complete understanding of the mechanistic basis of drive and its suppression has been elusive (Grognet et al., 2014; Larracuente and Presgraves, 2012; Bauer et al., 2007, 2005; Hammond et al., 2012).
The prospect of characterizing meiotic drivers in a genetically tractable system spurred our study of a pair of fission yeasts, Schizosaccharomyces pombe strain 972 (Sp) and Schizosaccharomyces kambucha (Sk). Despite being 99.5% identical at the nucleotide level, Sp/Sk hybrids are nearly sterile (Rhind et al., 2011; Zanders et al., 2014); a reproductive barrier between these yeasts must have arisen very recently. This rapid evolution of infertility is common amongst fission yeasts that are generally categorized as isolates of the Schizosaccharomyces pombe species (Avelar et al., 2013). In the case of Sp/Sk hybrids (and likely other pairings), the infertility is caused by both chromosomal rearrangements and multiple meiotic drivers (Zanders et al., 2014; Avelar et al., 2013). Indeed, we previously found that genes on each of the three Sk chromosomes are capable of enacting gamete (spore)-killing meiotic drive against their Sp homologs (Figure 1A) (Zanders et al., 2014). However, the genes responsible for the drive phenotypes were unknown.
Here, we use genetic mapping to identify Sk wtf4 as an autonomous gamete-killing meiotic drive gene. We show that Sk wtf4 generates two transcripts from alternative start sites: a long transcript encoding an antidote and a short transcript encoding a gamete-killing poison. Whereas the poison protein is found in all the gametes, the antidote protein is enriched only in the gametes encoding Sk wtf4, thereby ensuring that gametes that do not inherit the selfish allele are destroyed. This gene is a member of the large, rapidly evolving wtf gene family that has 25 members in Sp. We show that wtf4 is not the only driver amongst wtfs and propose a model in which meiotic drive is the ancestral function of the gene family. Our study thus identifies a novel mechanism by which meiotic drivers can act and highlights the significant role these selfish elements have played in shaping the evolution of a model eukaryote.
To study meiotic drive in fission yeast, we mate haploids to generate diploids, induce the diploids to undergo meiosis and monitor allele transmission into the gametes using genetic markers. In Sk/Sp hybrid diploids, drive of loci on all three Sk chromosomes is due to the preferential death of gametes inheriting the corresponding Sp alleles (Zanders et al., 2014) (Figure 1A). In this work, we focused on chromosome 3 because it is the smallest chromosome and the drive phenotype is strong: greater than 80% of viable haploid gametes inherit an Sk marker allele from Sk/Sp hybrids (Zanders et al., 2014).
To genetically map a drive locus on chromosome 3, we first wanted to generate a strain with Sk chromosomes 1 and 2, but Sp chromosome 3. Because Sp and Sk have different karyotypes on chromosomes 2 and 3 due to a translocation (Zanders et al., 2014), we could not generate such a strain as it would lack essential genes. Instead, we generated a haploid strain with an Sk karyotype containing Sk chromosomes 1 and 2 and most, but not all, of chromosome 3 derived from Sp (Figure 1—figure supplement 1 and Materials and methods). We then backcrossed this haploid strain to Sk to generate a series of haploid strains that have mosaic (Sp and Sk-derived DNA sequences) versions of chromosome 3 generated by recombination (Figure 1B). We then crossed the recombinant haploids to Sk to generate a series of ‘introgression diploids’ (Figure 1B and Figure 1C, diploids 1–8). The introgression diploids were all homozygous null mutants for rec12, the fission yeast ortholog of Sachharomyces cerevisiae SPO11, which is required for inducing DNA breaks to initiate meiotic recombination (Phadnis et al., 2011). As meiotic recombination is not induced in the introgression diploids, we could use any genetic marker on chromosome 3 to assay this chromosome for the presence of drive loci. We used the codominant markers ade6+ and ade6∆::hphMX4 to follow transmission of each chromosome into viable gametes (Figure 1C).
We observed three phenotypic classes amongst our introgression diploids (diploids 1–8, Figure 1C). In the first class (diploids 1–3), the allele from the pure Sk chromosome exhibited drive over the allele from the Sp/Sk mosaic chromosome. In the second class (diploids 4–7), we were surprised to observe the opposite phenotype: the allele from the Sp/Sk mosaic chromosome exhibited drive over that from the pure Sk chromosome. In the third class (diploid 8), we observed unbiased allele transmission.
Our finding of three distinct phenotypic classes amongst our introgression diploids (diploids 1–8) is inconsistent with the simple model of a single drive locus on Sk chromosome 3. A single gene model predicts two phenotypic classes: (1) introgression diploids in which the pure Sk chromosome exhibits drive because the Sk/Sp mosaic chromosome lacks the Sk drive allele and (2) introgression diploids in which the chromosomes show Mendelian transmission because the Sk/Sp mosaic contains the Sk drive allele.
Instead, our data are more consistent with the presence of a meiotic drive allele (or alleles) found on both Sk and Sp chromosome haplotypes and the existence of at least one genetically separable drive suppressor. The drive of the Sk/Sp mosaic chromosome over the pure Sk chromosome in class 2 (diploids 4–7) is consistent with the presence of an Sp drive allele in these strains. The full effects of this Sp drive locus could have been missed previously in Sk/Sp hybrid crosses due to the actions of an Sp drive suppressor not found in the class 2 introgressions (Zanders et al., 2014).
Similar to what we previously observed in crosses between pure Sk/Sp hybrids (both rec12+ and rec12∆), we found that viable gametes produced by diploids of all three classes frequently inherited both alleles at the ade6 locus (Figure 1C) (Zanders et al., 2014). This indicates that they are not haploid at this locus, as is expected for gametes. These gametes likely represent a mix of heterozygous diploids and heterozygous chromosome 3 aneuploids. In diploid 8, the phenotype was extreme, with almost all the viable gametes inheriting both ade6 alleles (Figure 1C). Although the frequency of meiotic chromosome missegregation is elevated in rec12∆ mutants (Phadnis et al., 2011), we see significantly higher levels of viable gametes that inherit both alleles in diploids 1–8 than we did in a homozygous Sk rec12∆ control (Figure 1C, diploid 10).
The high level of chromosome 3 aneuploidy and/or diploidy we observe in the viable progeny of Sk/Sp hybrid crosses and our introgression diploids (1-8) is also consistent with the existence of both Sk and Sp active meiotic drive loci. We previously showed in Sk/Sp hybrids that this phenotype was not due to elevated chromosome missegregation in meiosis, but rather preferential death of haploid gametes (Zanders et al., 2014). As we proposed previously, this phenotype could result from distinct competing Sk and Sp driver loci on chromosome 3 (Zanders et al., 2014; Bomblies, 2014). In the absence of recombination, a given haploid gamete can inherit only the Sk or Sp drive locus and is thus sensitive to being killed by the one it does not inherit. Heterozygous diploids and heterozygous aneuploids, however, would inherit both loci and be resistant to both killers.
To map driver location(s) from the phenotypic data described above, we sequenced the haploid strains that contributed the Sk/Sp mosaic chromosomes to the introgression diploids (diploids 1–8) and combined genotype information with the phenotypic data described above. We determined which regions of chromosome 3 were derived from Sk and which were from Sp in each strain (Figure 1C and Figure 1—source data 1). It was clear from our data that one or two loci are not sufficient to explain the phenotypes of all these strains.
We chose to focus on the Sk/Sp mosaic chromosome found in diploid 1. This strain has the smallest amount of Sp DNA (~180 kb), and drive of Sk in the introgression/Sk diploid suggested the strain lacks a drive allele found in Sk (Figure 1C). We crossed a haploid isolate containing this chromosome to a rec12+ Sk strain to generate recombinant progeny containing smaller segments of Sp-derived DNA (Figure 1D and Materials and methods). We SNP-genotyped those recombinants and tested their phenotypes by mating them to Sk to generate additional introgression diploids (see Materials and methods). We selected diploid 9 for further analysis, as it contains the Sk/Sp mosaic chromosome with the smallest region of Sp-derived DNA (~30 kb) that a pure Sk chromosome can drive against (Figure 1C and Figure 1D). After excluding aneuploid/diploid progeny (those that inherit both ade6 markers), the allele from the pure Sk chromosome shows essentially the same transmission bias in diploids 1 and 9. These results suggest the Sk drive allele active in diploid 1 is found in this ~30 kb region. Curiously, this locus is in a region that is transmitted in a Mendelian manner (to ~50% of progeny) in pure Sk/Sp hybrids (Zanders et al., 2014), suggesting that other loci can mask the effects of the driver within this ~30 kb region. In addition, it is unclear why the fraction of viable progeny that inherit both ade6 alleles drops between diploids 1 and 9. These puzzles likely reflect the complexity of the multiple drivers and suppressor loci acting in these yeasts (Zanders et al., 2014).
We next wanted to verify the candidate drive locus using a recombination-competent (rec12+) diploid. We generated introgression diploid 11 which contains the same Sk/Sp mosaic chromosome as diploid 1, but is rec12+. To follow the transmission of the candidate locus, we needed a closely linked marker gene, so we engineered heterozygous markers at the linked ura4 locus (Supplementary file 1). We found that the ura4 allele from the pure Sk chromosome is transmitted to 87% of the viable gametes produced by diploid 11, which is not significantly different from the 88% transmission of the Sk allele in diploid 1 (Figure 1C and Figure 2A). This result shows that ura4 is closely linked to an Sk drive locus and is consistent with that locus being within the ~30 kb candidate region.
To test whether the transmission bias we observed in diploid 11 might be caused by increased cell death amongst gametes inheriting the Sp locus, we used propidium iodide (PI) to stain the meiotic sacs (asci) that hold the spores. PI efficiently stains dead cells that have lost their membrane integrity but fails to stain viable cells (Figure 2B and Figure 2—source data 1) (Moore et al., 1998). We found that only 81% of spores generated by diploid 11 excluded PI, while wild-type strains (e.g. diploid 13) have rates >90% (Figure 2A). Together, our findings support the hypothesis that the Sk ~30 kb region encodes a gamete-killing meiotic driver.
Near the center of the Sk 30 kb candidate region is wtf4 (Figure 1D), a member of the mostly uncharacterized wtf gene family. This family contains 25 members in Sp, and its (cheeky) name is derived from the genes’ genomic association with Tf transposons (Bowen et al., 2003). wtf genes are not found outside Schizosaccharomyces species (Bowen et al., 2003). Sk wtf4 is a 1427 bp gene (from the start to stop codon, including introns) with six exons and encodes a protein with six predicted transmembrane domains. Sk wtf4 shares only 89% DNA sequence identity (82% amino acid identity) with the gene in the orthologous locus in Sp (Sp wtf4); this divergence is much higher than expected given the 99.5% average DNA sequence identity between the two genomes (Rhind et al., 2011; Zanders et al., 2014). We reasoned that wtf genes, in general, were good candidates for meiotic drive loci because of their rapid evolution and their transcription during meiosis (Bowen et al., 2003; Mata et al., 2002; Daugherty and Malik, 2012; McLaughlin and Malik, 2017).
To test if Sk wtf4 is a meiotic drive gene, we deleted Sk wtf4 (Sk wtf4Δ) in a pure Sk background and mated that haploid to one containing the same Sk/Sp mosaic found in diploid 11 (Figure 2A) to produce diploid 12. We observed a significant increase in the number of spores that could exclude PI in diploid 12 (Sk wtf4Δ), compared to diploid 11 (Sk wtf4+) from 81% to 96%, suggesting Sk wtf4+ promotes spore death in progeny of heterozygous diploids. In addition, Sk wtf4Δ showed more equitable allele transmission. While Sk wtf4+ is transmitted to 87% of the viable gametes produced by diploid 11, the transmission rate of Sk wtf4Δ is reduced to 66% in diploid 12 (Figure 2A). Although some residual transmission bias remains in this background, our results clearly implicate Sk wtf4 as a large contributor to gamete-killing meiotic drive.
There are two known means by which gamete-killers act to eliminate competing alleles (Lindholm et al., 2016; McLaughlin and Malik, 2017). Under one model, meiotic drivers kill gametes containing a particular target locus. For example, the Segregation Distorter (SD) system in Drosophila melanogaster kills sperm bearing an expansion of the Responder satellite DNA (Larracuente and Presgraves, 2012; Wu et al., 1988). The second model is a poison-antidote model in which a gamete-killing entity (the poison) is encoded at a position that is closely linked to that encoding a second substance (the antidote) which specifically protects gametes that inherit the drive locus. For example, the unidentified rfk gene (required for killing) acts as a poison and the rsk gene (resistance to spore killing) acts as an antidote in the Spore killer-2 drive locus from Neurospora intermedia (Hammond et al., 2012; Harvey et al., 2014).
We first tested if Sk wtf4 acts analogously to SD to kill gametes that inherit a particular Sp chromosomal locus. To test this idea, we analyzed the effect of Sk wtf4Δ/Sk wtf4+ heterozygosity in a pure Sk strain background (diploid 14, Figure 2A). As this Sk wtf4Δ/Sk wtf4+ heterozygote contains no Sp DNA, there should be no drive if wtf4 can only target and drive against Sp sequence. We did, however, observe strong drive (93% transmission) of Sk wtf4+ relative to Sk wtf4Δ in diploid 14 and a concomitant decrease in the percent of spores that could exclude PI (59% versus 92% in wild-type; Figure 2A, diploids 14 and 13). These results demonstrate that the drive of Sk wtf4 does not require an Sp target sequence.
Our results are, however, consistent with a poison-antidote model of meiotic drive. The phenotype of the Sk wtf4Δ/Sk wtf4+ heterozygote (Figure 2A, diploid 14) suggests that Sk wtf4 acts as the antidote because gametes lacking the gene die. If this were true and a separate gene acted as the poison, we predicted that Sk wtf4Δ homozygotes (diploid 15) should have very low fertility because they would generate a poison, but no antidote. Contrary to this expectation, we found that an Sk wtf4Δ homozygote is healthy, with the same ability to exclude PI from the spores as wild-type Sk (92% of spores; Figure 2A, diploids 13 and 15). This finding rules out the possibility that Sk wtf4 encodes a gene important for meiosis or spore development. Instead, our results suggest that Sk wtf4 acts as both poison and antidote, similar to the Spok genes of Podospora anserina (Grognet et al., 2014).
It remains unclear, however, why the phenotype of Sk wtf4 is slightly weaker in the hybrid background (assayed in diploids 11 and 12) compared to the phenotypes in pure Sk (diploids 13–15) or pure Sp (diploids 16–18). We speculate it could be due to the composition (chromatin state or a sequence variant) of the mosaic chromosome (allele 2 in diploids 11 and 12).
To further test the idea that Sk wtf4 encodes an autonomous poison-antidote drive locus, we moved the gene to a naive genome and tested if it could induce drive. We integrated Sk wtf4 into the Sp genome at the ade6 locus, which is unlinked to the endogenous wtf4 locus. An Sp diploid that is hemizygous for Sk wtf4 (Sk wtf4+/ade6+) produced fewer viable spores (54% PI-excluding spores, versus 96% in the vector-only control) and showed a marked transmission bias (96%) favoring Sk wtf4+ (Figure 2A, diploids 16 and 17). In contrast, Sp diploids homozygous for Sk wtf4+ produced viable spores that excluded PI at the same frequency as spores from wild-type diploids and showed unbiased allele transmission (Figure 2A, diploids 18 and 16). These results are consistent with Sk wtf4 acting as a complete one-gene poison-antidote drive system that causes the death of gametes that fail to inherit the locus from heterozygotes.
We hypothesized that Sk wtf4 encodes two products to achieve drive (Figure 3A). The first of these is a gamete-killing poison, which acts indiscriminately on all spores. The second product is an antidote that specifically rescues only the gametes encoding Sk wtf4 from the poison. To investigate how Sk wtf4 could make two products, we analyzed long-read sequence data from Sp meiotic mRNAs (Kuang et al., 2017) (Materials and methods). This revealed that Sp wtf4 is transcribed during meiosis and generates two major overlapping transcripts with different start sites (Figure 3—figure supplement 1). Since the region starting 500 bp upstream of the annotated Sp wtf4 start codon until the putative second start codon is fairly well conserved (98% identical) between Sp and Sk wtf4, we hypothesized that Sk wtf4 is likely to produce similar alternate isoforms to Sp wtf4. These alternative transcripts of Sk wtf4 could encode the two meiotic drive components – a poison and an antidote (Figure 3B).
To test the feasibility of our model, we investigated the localization of Sk Wtf4-GFP in Sp diploids induced to undergo meiosis (Sheff and Thorn, 2004). We C-terminally tagged the gene to visualize proteins generated by both the putative Sk wtf4 isoforms; this tag does not interfere with Sk wtf4’s ability to function as a drive allele (see data for ‘GFP diploid’ in Supplementary files 1 and 2). Visualizing Sk wtf4-GFP/ade6+ heterozygous diploids, we observed faint cytoplasmic Wtf4-GFP signal before the first meiotic division, which intensified throughout gamete development and filled the ascus surrounding the mature gametes (Figure 3C). In mature asci, we observed a strong enrichment of Wtf4-GFP within only two of the four spores. We observed the same spore enrichment pattern in Sk wtf4-GFP/Sk wtf4+ diploids in which drive does not occur (Figure 3C).
We hypothesized that the diffuse Wtf4-GFP localization in the ascus corresponded to the poison, whereas the enrichment within the mature spores might reflect the localization of the antidote. If this hypothesis is correct, Wtf4-GFP should be enriched in the two spores that inherit the chromosome carrying Sk wtf4-GFP. Consistent with this idea, we stained asci from Sk wtf4-GFP/ade6+ diploids with PI and observed that the surviving PI-negative spores (95% of which inherit Sk wtf4-GFP) are indeed those with the strong Wtf4-GFP signal (Figure 3D; Supplementary file 1). The localization pattern of Wtf4-GFP is consistent with our model of Sk wtf4 encoding two protein isoforms (Figure 3A).
To further test our poison-antidote model, we sought to generate alleles that could produce only the poison or only the antidote. We first mutated the start codon (ATG to TAC) that is present only in the putative short transcript. Our results (below) suggest that this mutant allele retains the antidote function but no longer functions as a poison: we therefore call this allele Sk wtf4antidote (Figure 4A). In hemizygous diploids (Sk wtf4antidote/ade6+), Sk wtf4antidote does not cause spore death (increased frequency of PI-stained spores) or the transmission bias that is observed with the wild-type Sk wtf4 allele, suggesting that the mutant can no longer drive (compare Figure 4B, diploid 20 to Figure 2A, diploid 17). However, this allele still protects from meiotic drive since Sk wtf4+/Sk wtf4antidote heterozygotes produce PI-excluding spores at the same frequency as wild-type and show unbiased allele transmission (Figure 4B, diploid 21). These data assign an antidote function to the long transcript.
We next set out to generate a Sk wtf4poison allele by mutating the two putative start codons (ATG to TAG) found in exon 1 of the long transcript (Figure 4A). This mutant should be able to generate only the short polypeptide. If this allele retains the ability to poison spores but has lost the antidote function, we would expect all progeny to be killed in Sk wtf4poison/ade6+ hemizygotes. Indeed, most spores generated by these diploids die (14% exclude PI stain, Figure 4B, diploid 22). Interestingly, the Sk wtf4poison allele was modestly underrepresented (38% transmission) in the few surviving spores generated by diploid 22, indicating that the spores that inherit that allele are especially likely to be destroyed by their own poison (Figure 4B).
To confirm that the toxicity of the Sk wtf4poison allele was due to its lacking the Sk wtf4 antidote, we generated Sk wtf4poison/Sk wtf4+ heterozygotes. As expected, the spores that inherited the complete Sk wtf4+ gene from these diploids were immune to Sk wtf4poison toxicity, while those that inherit Sk wtf4poison die. (Figure 4B, diploid 23). These results support our model that the short Sk wtf4 transcript encodes a trans-acting gamete poison.
As a final test of our model, we brought the separated poison and antidote mutant alleles back together in one diploid, but on opposite haplotypes. If they function as expected, we would predict that the Sk wtf4poison spores will die but the spores that inherit the Sk wtf4antidote will survive. This was indeed the case. Only 45% of the spores produced by Sk wtf4antidote/Sk wtf4poison heterozygotes can exclude PI stain and 88% of the surviving gametes inherit the Sk wtf4antidote allele (Figure 4B, diploid 24).
We next specifically determined the localization patterns of the antidote and poison polypeptides. To visualize the antidote peptide, we generated an Sk mCherryantidote-wtf4 allele (Figure 5A) and found it acts similarly to the wild-type wtf4 allele (Figure 5B, diploids 25 and 26) (Hailey et al., 2002). We could not reliably use PI staining to assay fertility of mCherry-tagged strains because both signals are red, so we used viable spore yield assays (VSY) (Smith, 2009) to confirm that the fertility of the Sk mCherryantidote-wtf4 allele was similar to untagged wtf4 in heterozygotes. Sk mCherryantidote-wtf4/ade6+ hemizygotes had a VSY of 0.8 ± 0.2 (standard deviation) compared to 1.0 ± 0.4 of Sk wtf4+/ade6+, and Sk mCherryantidote-wtf4/wtf4+ diploids had a VSY of 1.4 ± 0.1 compared to 1.7 ± 0.1 of wild-type.
To observe the localization of the poison peptide, we generated a Sk wtf4poison-GFP allele (Figure 5A) (Sheff and Thorn, 2004). While this Sk wtf4poison-GFP allele is not as penetrant as the untagged Sk wtf4poison allele, it does have a poison-only phenotype (Figure 5B, diploids 27 and 28). In Sk mCherryantidote-wtf4/ Sk wtf4poison-GFP heterozygotes, we observed Sk Wtf4poison-GFP expression before the meiotic divisions and later filling mature asci. In contrast, we observe Sk mCherryantidote-Wtf4 enriched only in two of the four mature spores (Figure 5C). Together, these data reconstitute the dual localization patterns we observed with Sk Wtf4-GFP and support our model of a poison-antidote system encoded by the same gene (Figure 3A).
We hypothesized that if Sk wtf4 is not unusual amongst the wtf genes in its ability to drive; meiotic drive could explain the ‘driving’ force behind the expansion of the wtf gene family (Bowen et al., 2003). The large number of wtfs could also explain the complex drive landscape revealed in our recombination mapping (Figure 1). To test these ideas, we analyzed additional wtf genes from Sk.
We cloned and tested six Sk wtf genes (wtf2, wtf5, wtf6, wtf28, and wtf21 plus wtf26 [together]) for evidence of meiotic drive. As for our tests of Sk wtf4, we integrated the above Sk wtf genes at the ade6 locus of Sp, which disrupted the ade6+ gene. We then mated those haploids to ade6+ to generate heterozygous diploids and monitored the transmission of the Sk wtf gene(s) into viable progeny using the heterozygous ade6 markers. Five of the six genes had no observable drive phenotype. Sk wtf2 was transmitted to 47% (n = 114) of progeny, Sk wtf5 was transmitted to 44% (n = 454), Sk wtf6 was transmitted to 51% (n = 471) and the combination of Sk wtf21 and wtf26 (cloned and integrated together) was transmitted to 46% (n = 111). However, like Sk wtf4, Sk wtf28 caused strong drive (90% transmission bias and only 57% of spores excluded PI; Figure 2A, diploid 19).
We also compared the sequence of each of these Sk wtf genes to the Sp wtf genes at the syntenic loci. wtf26 and wtf28 are not found in Sp, so have either been lost in Sp, or gained in Sk since divergence. While Sk wtf2 is a 1036 bp full length gene, Sp wtf2 is likely a 388 bp pseudogene (it has a large deletion relative to other wtf genes and multiple in-frame stop codons). Sk wtf21 is likely a pseudogene (multiple in frame stop codons), whereas Sp wtf21 is intact. The two loci share 83% DNA sequence identity. The wtf5 gene is intact in both species, and the loci share 99% DNA sequence identity and 97% amino acid identity. Sp and Sk wtf6 share 82% nucleotide identity, but only 74% amino acid identity. Altogether, the wtf loci show much greater sequence divergence than the 99.5% genome average identity between Sp and Sk. Such rapid evolution is a hallmark of genes involved in genetic conflicts, such as loci involved in causing or suppressing meiotic drive (Daugherty and Malik, 2012; McLaughlin and Malik, 2017; Henikoff et al., 2001).
Intriguingly, the Sk wtf28 drive gene is also the only one of the six genes we tested that also has a putative alternate start codon in exon two that could be used to make a putative short poison isoform. Additionally, Hu et al., 2017 also identified two different wtf drivers in another Sp isolate (CBS5557) and both have a potential alternate start codon in exon 2. Of the 25 wtf loci in Sp, four (wtf4, wtf13, wtf19 and wtf23) also appear to be capable of encoding two proteins and we predict these are active drive genes. In contrast, the intact genes we tested that did not confer drive, Sk wtf2, wtf5, wtf6, and wtf26, all encode genes similar to the antidote isoform of Sk wtf4 but appear to lack a shorter poison isoform. Together, our results and those of Hu et al., 2017) are consistent with the hypothesis that the ancestral function of the wtf family is to confer meiotic drive.
Our study demonstrates that Sk wtf4 is a novel, gamete-killing meiotic drive locus. Like the Spok family of drivers found in Podospora, wtf4 is an autonomous drive system that confers both the ability to kill gametes that do not inherit the gene and the ability to protect the gametes that do (Grognet et al., 2014). We show that wtf4 achieves these disparate functions by a previously undescribed mechanism in which the gene encodes a poison protein from one transcriptional start site and an antidote protein from an alternative transcriptional start site. We show that the poison protein is trans-acting and has the capacity to destroy all gametes, but that the antidote remains in the gametes that inherit the wtf4 locus and specifically rescues them from destruction.
The poison-antidote mechanism of Sk wtf4 is comparable to the bacterial toxin-antitoxin (TA) systems. These systems are found in most prokaryotes and have been extensively studied. TA systems consist of a toxin that will prevent cell growth or viability and an antitoxin that neutralizes the toxin using a wide variety of mechanisms, typically being classified into six different types (Lee and Lee, 2016). Interestingly, some toxins are stable, transmembrane proteins that act by disrupting membrane integrity and are counteracted by either an unstable small RNA (Lee and Lee, 2016; Unterholzner et al., 2013) or a protein that degrades the toxin mRNA (Wang et al., 2012). In our poison-antidote meiotic drive system, Sk wtf4 creates two putative trans-membrane proteins: a trans-acting poison and spore-specific antidote. While the exact mechanism of toxicity of Wtf4poison is unknown, we hypothesize that it could be disrupting membrane integrity in a similar manner to the membrane-lytic toxins of some TA systems (Lee and Lee, 2016; Unterholzner et al., 2013). In contrast, we speculate that Wtf4antidote protects the spores that inherited Sk wtf4 by sequestering the poison for degradation. The spore specificity of Wtf4antidote could be due to late translation or a spore retention signal within exon 1, because that is the only region that Wtf4poison is lacking. In addition, work by Hu et al. suggests that the C-termini of Wtf proteins may be more important for the poison than for the antidote functions, despite both proteins being generated by a single given wtf gene sharing a common C-terminus (Hu et al., 2017).
Outside of its role in meiotic drive, wtf4 has no apparent role in promoting fertility (Figure 2A, diploid 15). Instead, the gene causes about half of all gametes to be destroyed in heterozygotes. In other words, the wild-type allele of wtf4 causes infertility to promote its own fitness. This puts wtf4 into a state of genetic conflict with the rest of the genome because infertility is clearly bad for fitness of loci unlinked to wtf4. Unlinked variants that can suppress drive would be favored by natural selection because they increase fitness (Crow, 1991). Novel wtf4 variants that can evade this suppression to reestablish drive would then be favored. This evolutionary dynamic is analogous to that observed between viruses and host immune systems and is well known to foster a ‘molecular arms race’ in which both sides must continually innovate (Daugherty and Malik, 2012; McLaughlin and Malik, 2017). Consistent with the idea that the gene is locked in such an arms race, the DNA sequence divergence between Sk and Sp at the wtf4 locus is more than 20-fold higher than the genome-wide average (Rhind et al., 2011; Zanders et al., 2014).
The evolution of wtf4 elicits the question of how the gene can rapidly evolve while maintaining specificity between the poison and antidote it encodes. Uncoupling these components leads to sterility, an evolutionary dead end. It is possible that such variants do arise and are quickly purged from populations. We propose, however, that the coding sequence overlap between the poison and antidote could promote specificity between the two components, for example, by the antidote acting as a dominant suppressor of the poison. In this manner, the poison could diverge without losing the self-protection conferred by the antidote. Using a shared sequence to confer specificity between drive components may be a recurring theme amongst gamete-killers. In their analyses of Podospora Spok genes, Grognet and colleagues found that they could generate antidote-only alleles and a partial poison-only allele via C- and N-terminal tagging of the proteins, respectively. They were not, however, able to generate separation of function alleles of Spok1 by making N- or C- terminal deletions (Grognet et al., 2014). Future work identifying the molecular mechanisms of both families of drivers will be required to test the idea that the fact that the poison and antidote are encoded by overlapping sequences minimizes the probability of disrupting their specificity.
Combined with our previous work, the varied phenotypes of our Sp chromosome 3 introgressions reveal a complex landscape of meiotic drive loci in the Sk and Sp genomes (Zanders et al., 2014). As Sk wtf4 is a member of the large wtf gene family, the most likely candidates underlying these other drive loci are wtf genes. For example, there are >20 wtf loci on Sp (and likely Sk) chromosome 3 that could contribute to the complex drive phenotypes we observe (Figure 1) (Bowen et al., 2003). Consistent with the idea that the Sk wtf4 is not unique in its ability to drive, we showed that Sk wtf28 can also cause drive and Hu and colleagues demonstrate that two additional wtf genes from another isolate of the Sp family also cause meiotic drive (Hu et al., 2017).
Although not all wtfs are capable of autonomously causing meiotic drive, their rapid evolution is still consistent with their involvement in meiotic drive (McLaughlin and Malik, 2017). We propose that different wtf genes represent distinct evolutionary stages. The putative ancestral type (Sk wtf4 and wtf28) are still active as meiotic drivers and encode both poison and antidote proteins. The next stratum represents genes (Sk wtf2, wtf5, wtf6 and wtf26) that have lost poison, but not antidote function. As we have shown for the Sk wtf4antidote allele, such alleles are unlikely to cause meiotic drive as they have lost their poison-coding capacity, but they still have protective function against the ancestral drive allele and thus may have been selectively retained as ‘domesticated parasites.’ Over time, when the protective function is no longer beneficial and selected for (e.g. if the ancestral drive allele is lost from the population), such antidote genes may also eventually degenerate. Therefore, the final stratum represents putative wtf pseudogenes such as Sk wtf21, in which both the poison and antidote function have decayed.
There are 25 wtf loci in the Sp genome and this work combined with that of Hu and colleagues implicates these genes in causing and/or modifying meiotic drive (Bowen et al., 2003; Hu et al., 2017 ). Meiotic drive has therefore played a significant role in the evolution of the Sp group of fission yeasts, despite the heavy fitness costs these selfish loci can levy. It is striking to consider how long these selfish genes went undetected in such a simple and intensely studied organism. How many more such parasites are lurking undetected in eukaryotic genomes?
For the mapping crosses, fertility and meiotic drive assay, the crosses were carried out similar to the description in Zanders et al. (2014). This required making stable diploids, because many of the strains used are homothallic (h90) and their self-mating would generate many non-informative spores. Briefly, we mixed ~200 µL of overnight culture from each haploid parent in a microcentrifuge tube, spun down the cells and plated them on either SPA (1% glucose, 7.3 mM KH2PO4, vitamins, agar) or MEA (3% malt extract, agar) for 12–15 hr at room temperature to allow the cells to mate. We observed no differences in meiotic drive phenotypes for diploids generated on SPA vs. MEA. We generally use SPA, but for some matings have more success isolating stable diploids from MEA. We scraped off the mated cells and spread them on a medium to select heterozygous diploids (generally minimal yeast nitrogen base plates). We grew diploid colonies overnight in 5 mL of rich YEL broth (0.5% yeast extract, 3% glucose, 250 mg/L of adenine, lysine, histidine, leucine, and uracil). We then plated a small amount of the cultures ≤100 µL onto SPA to induce sporulation, and plated a diluted sample onto YEA (same as YEL, but with agar). We screened the colonies that grew on the YEA plate via replica plating to diagnostic media to verify that the culture was comprised of heterozygous diploid cells. If not, the culture was not assayed further. After 3–7 days, we scooped up the mixture of cells, asci, and spores from the SPA plates, treated it with glusulase and ethanol to kill vegetative cells and to release spores from asci, and plated the spores on YEA. We then phenotyped the spore colonies using standard approaches. For some control loci, we could not easily verify heterozygosity in the diploid test described above. For these loci, we verified heterozygosity of the parent diploid in the progeny. If the parent diploid proved not to be heterozygous, the diploid was eliminated. For each cross, we assayed at least two independently created diploids. The number of progeny we scored varied between experiments. To map Sk wtf4, we assayed at least 100 viable progeny per cross. To characterize Sk wtf4, we assayed at least viable 200 gametes per cross. The one exception was the Sk wtf4poison/ Sk wtf4antidote cross in which we had to assay allele transmission by PCR and sequencing (described below). For that cross, we assayed 50 viable progeny.
All strains used and their genotypes can be found in Supplementary file 3. We deposited sequencing data from all high-throughput sequencing to GenBank accession number PRJNA376152. We chose to map first a drive allele present on Sk chromosome 3 via recombination mapping. To eliminate the effects of drivers and gross chromosomal rearrangements from chromosomes 1 and 2, we began the mapping effort using a strain (SZY558) that contains chromosomes 1 and 2 from Sk, but in which most of chromosome 3 was derived from Sp (the mosaic chromosome illustrated in Figure 1B is from SZY558). We could not use a complete Sp chromosome 3 because such a strain lacks essential genes due to a translocation between chromosomes 2 and 3 that occurred in the Sk lineage (Zanders et al., 2014). Sequencing revealed that chromosome 3 in SZY558 was generated by a crossover event between Sp and Sk chromosomes somewhere between positions 1,804,477 and 1,810,659 on the Sp chromosome. The region to the right of this point contains Sk alleles and the strain has the Sk karyotype (Figure 1B).
The generation of SZY558 is described in Figure 1—figure supplement 1. We first crossed SZY201 (Sp) to SZY208 (Sk) to generate SZY239 and SZY247. Although no recombination was expected in this cross because the two parental strains are rec12∆, both SZY239 and SZY247 must contain a recombinant chromosome 2 and/or a recombinant 3 because they inherited non-parental combinations of markers on chromosomes 2 and 3, and the two species karyotypes are incompatible (Zanders et al., 2014; De Veaux et al., 1992). Such recombinant spores are quite rare (Zanders et al., 2014) but were obtained via selection for a nonparental combination of markers on chromosomes 2 and 3 (e.g. His+ hygromycin resistant). Most such selected progeny are chromosome 3 aneuploids, so we then streaked the strains to single colonies to allow them to lose the additional copy of chromosome 3. We crossed SZY239 to SZY247 to generate a strain (SZY382) that contained the recombinant chromosome 3, but also had the lys1-37 and his5+ markers on chromosomes 1 and 2, respectively. The lys1-37 and his5+ markers in this strain were useful for following chromosomes 1 and 2 in a subsequent cross. We transformed SZY382 with a PCR fragment generated with oligos 255 and 256 using plasmid pAG32 as a template to generate a strain (SZY547) with arg12∆::hphMX4 (Goldstein and McCusker, 1999). The arg12 locus is on chromosome 3 in Sk and in strain SZY547, which has the Sk karyotype. We then crossed SZY547 to SZY192 (Sk) to generate strain SZY558. The purpose of this cross was to move the recombinant chromosome 3 into a strain background with pure Sk chromosomes 1 and 2 (marked with lys1+ and his5∆::natMX4).
For mapping Sk wtf4, we crossed SZY558 to a differentially marked Sk strain (SZY210) to generate recombinant haploid progeny (introgression strains) that contained a smaller fraction of chromosome 3 from Sp (Figure 1B). We used genetic markers (ura4, ade6 and arg12) to select only true haploid recombinants for our introgression strains. We mated the introgression strains and Sk (SZY196) to generate diploids 1–8 (Figure 1C). The mapping scheme was designed such that diploids generated by these matings were homozygous rec12∆, so recombination would infrequently separate the drive allele from the genetic markers used to distinguish the introgression and Sk chromosomes (De Veaux et al., 1992). We sequenced at least one introgression representing each phenotype we observed amongst these strains and distinguished Sp and Sk SNPs as in (Figure 1—source data 1) (Zanders et al., 2014).
SZY565 (the haploid parent that contributed the mosaic chromosome 3 to diploid 1 in Figure 1C) is the introgression strain that contains the smallest region of Sp-derived DNA, from position 55,555 to 237,572 (Figure 1—source data 1). The Sk chromosome drove against this introgression in test crosses. We assumed that whatever feature of the Sp genome (either the presence of a target of killing or the absence of an antidote to killing) that conferred the sensitive phenotype (i.e susceptibility to being destroyed by the Sk driver) must be within that region and, correspondingly, that the Sk drive allele must also be within or very near that region. This is because a drive allele that acts to kill gametes that do not inherit it should target the homologous locus or a closely linked site to prevent self-killing. A drive allele that killed gametes that inherit a locus not linked to the drive allele would be an evolutionary dead end because it would kill gametes bearing the drive allele as often as it would kill gametes bearing the competing allele.
To narrow in on the key drive locus, we crossed SZY565 to SZY196 (Sk) to get a strain (SZY649) with the same chromosome 3 as SZY565, but with his5+ rather than his5∆::natMX4 on chromosome 2. The ura4 locus, at position 116,726–115,589 on chromosome 3, is within the Sp-derived region. We added an additional marker (kanMX4) within the Sp-derived region at position 214,491 to generate strain SZY659. To do this, we first generated plasmid pSZB134 which contains ~1 kb of DNA (amplified from Sp genomic DNA with oligos 380 and 381) upstream of the target site (214,491) cloned into the BamHI and BglII sites of pFA6a, and ~1 kb of DNA (amplified with oligos 382 and 383) downstream of the target site cloned into the SacI and SpeI sites of the pFA6a (Wach et al., 1994). The transformation cassette was released from pSZB134 via NotI digest and used to make SZY659.
We then crossed SZY659 to a differentially marked Sk strain (SZY320; rec12+) and screened for haploid progeny that had experienced a crossover within the Sp-derived region between the ura4∆::natMX4 allele from SZY320 and the kanMX4 allele in SZY659 (Figure 1D). We tested nine such haploids by test crossing them to Sk (SZY196). Two haploids had an Sk-like phenotype in that they showed Mendelian transmission of the ura4 locus; the other six showed the sensitive phenotype. We genotyped SNPs of the haploids at a few sites within the region to roughly estimate where the recombination event(s) occurred (Zanders et al., 2014). Amongst the haploids with the sensitive phenotype, SZY679 and SZY685 have the most Sk-derived DNA: they contain Sp DNA only between position ~210,000 (between 207,954 and 210,312) to 237,572 (Figure 1C, diploid 9, Figure 1—source data 1). The two strains with the Mendelian phenotype (SZY684 and SZY686) contain very little Sp-derived DNA. The Sp DNA begins between positions 210,312 and 214,500 and ends before 215,926. Comparing these two classes suggested that the key drive locus is located between positions ~ 210,000 and 237,572 (but not within the small region surrounding ~214,000). The annotated features of this region include all or part of 10 genes plus one pseudogene in Sp (Figure 1D).
Using oligos MESZ176 and MESZ177, we amplified from Sk genomic DNA the region corresponding to the wtf3+wtf4 locus in Sp. The product amplified is at least 1.5 kb smaller than the corresponding product from Sp. We then sequenced the PCR product using oligos 557, 560, 565, 566, 567, 568, 569, 570, 595, 597, 598, 599, 601, 602, and 603 and assembled a 2943 bp contig. This sequence has been deposited to GenBank, accession number KY652738. We did a BLAST search comparing our Sk sequence contig to all Sp protein sequences and got Sp wtf13 and wtf4 as top hits. The Sk region contains only one wtf-like gene, whereas the Sp region has the complete wtf4 gene and the wtf3 pseudogene. As the Sk gene appears to be orthologous to Sp wtf4 based on synteny and sequence similarity, we named the gene Sk wtf4.
We used the Sp PacBio meiotic transcriptome sequences to predict intron-exon boundaries in Sk wtf4 (Kuang et al., 2017). The authors Kuang et al. (2017) kindly provided pre-publication access to ‘Iso-Seq’ consensus isoform sequences. wtf genes are not well-represented in the splice isoform summary tables generated for that study due to the very high nucleotide identity between wtf paralogs and stringent filtering of multiply-mapping reads. We therefore re-mapped Iso-Seq data to the Sp reference genome assembly using GMAP (Wu et al., 2016), reporting only alignments with ≥99% identity and covering ≥99% of the length of the isoform sequence, and using the parameter ‘--suboptimal-score 20’ to reduce secondary matches (this parameter choice successfully eliminates cross-mapping between wtf4 and wtf13). We used IGV (Thorvaldsdottir et al., 2013) to visualize splice isoforms for each gene. These data reveal a coding sequence that is slightly different from that of the currently annotated Sp wtf4 gene (http://www.pombase.org/spombe/result/SPCC548.03c). The long form of Sk wtf4 has six predicted exons and encodes a 337 amino acid protein with 82% amino acid identity to the 366 amino acid protein encoded by Sp wtf4. The TMHMM model predicts six transmembrane helices with high probability (>80%) and one with lower probability (<50%) (Krogh et al., 2001).
To generate the Sk wtf4∆ mutant, we used the CRISPR-Cas9 system after first failing to generate the mutant via the standard homologous recombination approach (Jacobs et al., 2014). This system requires the starting strain to be ura4- and leu1-. We generated an Sk mutant (SZY661) in which leu1 was replaced with hphMX4 in strain SZY320. We did this by first cloning a leu1∆::hphMX4 cassette (pSZB136). We made this plasmid by first cloning leu1+ (amplified from Sk genomic DNA with oligos 413 and 414) into pFA6a cut with NdeI and ClaI and blunted with Klenow fragment of DNA polymerase I. This new vector was then cut with ClaI and NdeI (within leu1) and blunted with Klenow: the hphMX4 cassette liberated from pAG32 with PvuII and ClaI was ligated into the gap (Goldstein and McCusker, 1999). Oligos 413 and 414 were used again to amplify the leu1∆::hphMX4 cassette for transformation.
To generate plasmid pSZB184, which encodes a guide RNA targeting the Sk wtf4 region, we annealed oligos 577 and 578 and cloned them into the CspCI site of pMZ283 (Jacobs et al., 2014) We used overlap-PCR to generate a repair cassette containing ~1 kb of homology upstream and downstream of the Sk wtf4 region flanking the kanMX4 cassette from pFA6a (Wach et al., 1994). We stitched together the products of PCRs generated with oligos 571 and 572, 575 and 576, and 573 and 574 to make the repair cassette. We then transformed strain SZY661 with pMZ222, pSZB184, and the repair cassette. We screened through Ura+ Leu+ transformants containing both plasmids for wtf4 deletions via PCR and sequencing. We found that strain SZY862 contained a deletion of wtf4, but unexpectedly was not resistant to G418. Sequencing of the region revealed a truncation of the kanMX4 gene. SZY863 contains the same deletion as SZY862, but is Ura+ due to retention of the ura4+ cassette from pSZB184 at an unknown location closely linked to the endogenous ura4 locus, although the strain retains the ura4∆::natMX4 allele at the endogenous ura4 locus.
We first generated pSZB188, a plasmid containing the kanMX4 selectable marker and a mutant ade6 allele that has 5’, central, and 3’ deletions. This vector can be cut with KpnI within the mutant ade6 gene and then integrated into ade6+ to generate Ade- G418-resistant transformants. Other genes can be added to the vector to introduce them into the genome at the ade6 locus. To construct pSZB188, we first made a mutant ade6 cassette via overlap PCR stitching a PCR product made from oligos 588 and 589 to one made from oligos 591 and 590. This ade6 cassette was then digested with BamHI and XhoI and cloned into the BamHI and SalI sites of pFA6a (Wach et al., 1994). We cloned the Sk wtf4 region into pSZB188 by first amplifying the region with oligos 619 and 620. We digested the PCR product with SacI and cloned it into the SacI site of pSZB188 to generate pSZB189. We introduced KpnI-digested pSZB189 into yeast and selected transformants on YEA with G418 plates. We picked red colonies, as proper integrants should harbor a mutant ade6 allele flanking the sides of the plasmid sequence. The duplicated ade6 gene makes the locus unstable and Ade+ revertants that have ‘popped out’ all plasmid-derived sequences are readily obtained.
The Sk wtf4-GFP allele was made using overlap PCR. We amplified the promoter region from Sk genomic DNA using oligos 633 and 604 and the open reading frame sequence using oligos 605 and 606. We used pKT127 as a template to amplify yEGFP using oligos 607 and 634 (Sheff and Thorn, 2004). We then stitched the three PCR products together using overlap PCR. We cut the resulting cassette with SacI and cloned it into the SacI site of pSZB188 to generate pSZB204. This construct was integrated at ade6 as described above.
For the Sk wtf4antidote allele, using overlap PCR, we stitched together two PCR products generated with oligo pairs 735 and 686, and 620 and 736, both using pSZB189 as a template. We cloned the stitched PCR product into the SacI site of pSZB188 to generate pSZB246. We then cut pSZB246 and introduced it into yeast as described above.
We generated the Sk wtf4poison allele using overlap PCR. Sk wtf4 has two in-frame start codons in the annotated exon 1. Mutating the first start codon had no phenotype (data not shown), so we mutated both. To mutate the first start codon, we used overlap PCR to stitch together two PCR products made by oligo pairs 701 and 686 and 620 and 702; both reactions used pSZB189 as a template. The stitched PCR product was cloned into the SacI site of pSZB188 to generate pSZB244. We used pSZB244 as a template to mutate the second start codon via overlap PCR. We stitched together PCR fragments generated by oligo pairs 620 and 739 and 686 and 740 and cloned that product into the SacI site of pSZB188 to generate pSZB258. We cut pSZB258 and introduced it into yeast as described above.
We cloned the Sk mCherryantidote-wtf4 allele using overlap PCR. First, we purchased from IDT (Coralville, IA) a synthetic double-stranded DNA gene block including the Sk wtf4 promotor, the mCherry coding sequence (Hailey et al., 2002), five glycine codons, and the first part of Sk wtf4 exon 1. We amplified that fragment with oligos 620 and 604 and stitched that PCR product to another that contained the rest of the Sk wtf4 gene amplified with oligos 605 and 687 from plasmid pSZB189. We then cloned that product into the SacI site of pSZB188 to generate pSZB248, which we cut and introduced into yeast as described above.
For the Sk wtf4poison-GFP allele, we amplified the 5’ end of the gene with oligos 620 and 739 using plasmid pSZB244 as a template. We amplified the 3’ end of the gene with oligos 740 and 634 using pSZB203 as a template. We then used overlap PCR to stitch those PCR fragments together and cloned the product into the SacI site of pSZB188 to generate pSZB257, which we cut and introduced it into yeast as described above.
We used the same strategy to integrate other Sk wtf genes into Sp. We used Sk genomic DNA as a template to amplify wtf21+wtf26 with oligos 643 and 644, wtf2 with oligos 647 and 648, wtf5 with oligos 649 and 650, and wtf6+wtf28 with oligos 651 and 652. We cut each cassette with SacI and cloned them into the SacI site of pSZB188 to generate: pSZB209 (wtf21+wtf26), pSZB212 (wtf2), pSZB217 (wtf5), and pSZB215 (wtf6+wtf28). We subcloned Sk wtf6 and Sk wtf28 from pSZB215 by first amplifying the individual genes using oligo pairs 732 and 652, and 651 and 733, respectively. We then cloned the genes into the SacI site of pSZB188 to generate pSZB252 (wtf6) and pSZB254 (wtf28). All sequences of these genes have been deposited in GenBank, accession numbers KY652739-KY652742. These constructs were all integrated at ade6 as described above.
Because the alleles wtf4poison (SZY1051) and wtf4antidote (SZY1110) are marked with the same drug marker, to score transmission of alleles for this cross, we used sequencing. We generated diploids and spores as described above. We then plated the spores on YEA, picked the colonies to a YEA master plate and replicated to score control markers. We also prepared lysates for PCR from the master plate by scraping cells off the master plate into 20 µl of 20 mM NaOH. We boiled the cells for 5 min, froze them in liquid nitrogen, boiled again for 10 min, and spun the debris down. Using the supernatant lysate, we amplified the wtf4 region using oligos A01112 and 678. We then sequenced the exon 1 region using oligo 861. We analyzed the exon 1 region for the start codon mutations mentioned above (Figure 4A). If the exon 1 mutations were present, we quantified this as a poison allele; if not present, as an antidote.
To avoid ade6- mutant auto-fluorescence in cytology, we introduced ade6+ at the his5 locus. We amplified a region upstream of his5 to generate piece A using oligo pair 795 and 796. We amplified a region downstream of his5 to generate piece C using oligo pair 797 and 798, and to amplify ade6+ we generated piece B using oligo pair 799 and 800. We stitched together pieces A, B and C using oligo pair 795 and 798 and introduced the product into yeast.
For the fertility assay, we added 5–10 µl of propidium iodide (PI, 1 mg/ml) to 50 µl of H2O, and scraped the yeast from the SPA plate into the PI mix. We then incubated the yeast plus PI mixture at room temperature for 20 min. We took the images on a Zeiss (Germany) Observer.Z1 wide-field microscope with a 40x (1.2 NA) water-immersion objective and collected the emission onto a Hamamatsu ORCA Flash 4.0 using µManager software. We acquired the PI images with BP 530–585 nm excitation and LP 615 emission, using an FT 600 dichroic filter.
For all other fluorescence microscopy, we imaged on a LSM-700 AxioObserver microscope (Zeiss), with a 40x C-Apochromat water-immersion objective (NA 1.2), with 488 and 555 nm excitation. We collected GFP fluorescence through a 490–55 nm bandpass filter and mCherry fluorescence through a 615-nm longpass filter. The continuously variable secondary dichroic filter was positioned at 578 nm. We also imaged using a LSM-780 (Zeiss) microscope, with a 40x C-Apochromat water-immersion objective and 100x alpha Plan-Apochromat oil-immersion objective (NA 1.2 and 1.46, respectively), in photon-counting channel mode with 488 and 561 nm excitation. We collected GFP fluorescence through a 481–552 bandpass filter and mCherry through a 572 longpass filter. For all images acquired on the LSM-780 (Zeiss) microscope, using the same objectives as described above, we also imaged in photon-counting lambda mode, with 488 and 561 nm excitation. We collected fluorescence emission over the entire visible range. After acquisition, we linear unmixed the images using an in-house custom written plugin for ImageJ (https://imagej.nih.gov/ij/). Unmixing was achieved using spectra obtained from control cells. We did unmixing to verify that there was no auto-fluorescence in the cells (Figure 5—figure supplement 1) we scored. We did not score auto-fluorescent cells. Brightness and contrast is not the same for all images. We assayed at least 35 asci (but usually >100) for each genotype represented in Figures 3 and 5.
Genes in Conflict: The Biology of Selfish Genetic ElementsCambridge: Belknap Press of Harvard University Press.https://doi.org/10.4159/9780674029118
Rules of engagement: molecular insights from host-virus arms racesAnnual Review of Genetics 46:677–700.https://doi.org/10.1146/annurev-genet-110711-155522
Implementation of the CRISPR-Cas9 system in fission yeastNature Communications 5:5344.https://doi.org/10.1038/ncomms6344
Hybrid incompatibility genes: remnants of a genomic battlefield?Trends in Genetics 26:317–325.https://doi.org/10.1016/j.tig.2010.04.005
Predicting transmembrane protein topology with a hidden Markov model: application to complete genomesJournal of Molecular Biology 305:567–580.https://doi.org/10.1006/jmbi.2000.4315
The dynamic landscape of fission yeast meiosis alternative-splice isoformsGenome Research, 27, 10.1101/gr.208041.116, 27856494.
The ecology and evolutionary dynamics of meiotic driveTrends in Ecology & Evolution 31:315–326.https://doi.org/10.1016/j.tree.2016.02.001
The transcriptional program of meiosis and sporulation in fission yeastNature Genetics 32:143–147.https://doi.org/10.1038/ng951
Simultaneous measurement of cell cycle and apoptotic cell deathMethods in Cell Biology 57:265–278.https://doi.org/10.1016/S0091-679X(08)61584-8
The molecular evolutionary basis of species formationNature Reviews Genetics 11:175–180.https://doi.org/10.1038/nrg2718
Genetic analysis of meiotic recombination in Schizosaccharomyces pombeMethods in Molecular Biology 557:65–76.https://doi.org/10.1007/978-1-59745-527-5_6
IGV: high-performance genomics data visualization and explorationBriefings in Bioinformatics 14:178–192.https://doi.org/10.1093/bib/bbs017
Toxin-antitoxin systems: biology, identification, and applicationMobile Genetic Elements 3:e26219.https://doi.org/10.4161/mge.26219
A new type V toxin-antitoxin system where mRNA for toxin GhoT is cleaved by antitoxin GhoSNature Chemical Biology 8:855–861.https://doi.org/10.1038/nchembio.1062
GMAP and GSNAP for genomic sequence alignment: enhancements to speed, accuracy, and functionalityMethods in Molecular Biology 1418:283–334.https://doi.org/10.1007/978-1-4939-3578-9_15
Antonis RokasReviewing Editor; Vanderbilt University, United States
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This article reports analysis of a gene family that shows meiotic drive behavior. It's an extension of a previous paper by the senior author, who demonstrated the existence of meiotic drive elements in S. pombe/S. kambucha hybrids, but did not characterize these elements in detail. The current paper (and an accompanying paper from Hu et al.) identifies at least a subset of these drive elements as belonging to the wtf gene family, a group of repeated genes that tend to be found near transposable elements or their LTR remnants. This paper focuses on one of these genes, wtf4, and shows that the S. kambucha allele encodes a protein with two isoforms, a short form that encodes a spore-killing toxin that is expressed in meiotic cells before spore formation, and a long form that encodes an antidote that is expressed in a spore-specific manner. Further analysis identifies a second wtf locus in S. kambucha, wtf28, with similar gene structure and meiotic drive behavior. This, in combination with an accompanying paper (Hu et al.), provide a convincing case for the existence of multiple single-locus, toxin/antidote-type meiotic drive elements in the Schizosaccharomyces clade. Because of the novelty of this system, and because this work provides the first mechanistic insight into how a single-locus drive element can work, the paper is of considerable interest.
While the science in this paper is really exciting, the writing and presentation are sloppy and obtuse-it often feels as if the authors are having a conversation with themselves, and are focused on presentation rather than communication (these are not the same thing). This makes it a frustrating paper to read at more when one has an in-depth interest. More seriously, underlying experimental data are often needlessly absent or obscured.
1) Figure 1. One really has to hunt to figure out what the introgression diploids really are or how they were made. Since this is an online journal, why not illustrate their construction, and the chr 3 configuration within each diploid? This figure, like many others, uses terminology that is distant from the actual data. For example, "% aneuploid or diploid" "gametes" (Figure 1B) is not what was assayed – which was the fraction of viable spores that contain both parental chr 3 markers (but what were those markers?) and is thus a subset of possible disomic/diploid progeny (think uniparental disomy)?
In addition, part of the reason for the high level of chr 3 "disomy" among viable spores is because these are rec12-/rec12- diploids, which normally have a high degree of chr3 "disomy". This should be clearly communicated, and an Sk/Sk control (with suitably marked chrs 3) included to show the base level of chr 3 "disomy/diploidy" in rec12- mutants in the absence of any drive.
Another example – "% transmission Sk" – actually the fraction viable spores that only display one parental set of chr 3 markers, that display the "Sk" markers – but what were those markers? It's almost impossible to figure this out. Finally, data underlying Figure 1B and C are not presented at all, and need to be included in Supplementary file 1 (that is, once Supplementary file 1 is modified to make it clear and accessible, see below).
2) Figure 2, Supplementary file 1. The term "% fertility" is a misnomer. What is assayed is spores that fail to exclude PI; it's not even spore viability, since there are many ways a spore could not give rise to viable progeny yet still exclude PI. If authors can show that the vast majority of spores that exclude π give rise to colonies, then "fertility" is OK, but otherwise an operative term (i.e. "PI excluding") should be used.
3) Supplementary file 1. This table should include data from Figure 1 (see above). It absolutely requires a legend that explains what each column means (for example, N means 2 different things) and how the numbers were determined.
4) Figure 5. RNAseq data underlying the identification of two wtf4 transcripts should be presented.
5) Subsection “Expansion and rapid evolution of the wtf family is consistent with a role in meiotic drive”. Data and methods underlying the conclusions about the other wtfs that were tested should be presented, as these are important in vivo tests of the hypothesis. If diploids similar to diploid 9 in Figure 2 were made for the other wtfs, that data would be sufficient. It would also be nice (although not essential) if the authors could make a supplementary file that aligns all of the wtfs examined, to show where the two start sites are or are not. Since the RNAseq data for all the Sp wtfs are available, it would be interesting to know if the "tamed" wtfs only make the longer antidote mRNA, or if they still express both mRNAs. It would also be useful to ask which of the wtfs identified by Hu et al. (i.e. cws in CBS5557) are extant toxin-antidote systems using the dual start-site criterion, and which, if any, have degenerated to antidote-only; the same request will be made of Hu et al., so perhaps the two sets of authors could coordinate on this. It would also be useful to mention that Hu et al. have identified the C-termini of two wtf/cws loci in CBS5557as being important for toxin but not for antidote function.
6) There is a long history of toxin/antidote system in bacteria, which has been extensively reviewed. Adding a brief discussion of this to the Introduction or Discussion would add perspective to the article, and might offer some insight into possible wtf mechanisms.
7) Given that what the authors describe are gamete / spore killers, wouldn't it be more accurate to refer to the process as "drive" instead of as "meiotic drive" (following the recommendation of Burt & Trivers from their Genes in Conflict book – see page 16)? The phenomenon described has nothing to do with meiosis.
8) The authors need to be more sophisticated in their use of the concept of species. S. kambucha was so named on the basis of hybrid sterility <https://www.ncbi.nlm.nih.gov/pubmed/12399374> but is actually itself a mosaic of two strains of S. pombe (represented by 972 and NCYC132) which show greater sequence divergence from each other than either do from S. kambucha <https://www.ncbi.nlm.nih.gov/pubmed/21511999>. Thus, none of the three populations are genetically isolated on an evolutionary timescale. Therefore, be any modern definition of the term, S. pombe 972, S. pombe NCYC132 and S. kambucha are not separate species.
9) It would be of great interest to readers to have some speculation of how a putative trans-membrane protein could function in a toxin-antidote system and how the toxin comes to be distributed differently than the antidote.https://doi.org/10.7554/eLife.26033.023
- Gerald R Smith
- Gerald R Smith
- Sue L Jaspersen
- Sarah E Zanders
- Harmit S Malik
- Harmit S Malik
- Harmit S Malik
- Sarah E Zanders
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 T Levin and J Zeitlinger for comments on the manuscript, M Miller for assistance with the figures, Li-Lin Du for sharing results prior to publication, and three thoughtful reviewers (including Nick Rhind and Michael Lichten) for guiding improved data presentation. Original data underlying this manuscript can be accessed from the Stowers Original Data Repository at http://www.stowers.org/research/publications/libpb-1132. This work was supported by NIH R01 GM031693 and R35 GM118120 (GRS); NIH R01 GM74108, The Mathers Foundation, and HHMI (HSM); The Stowers Institute for Medical Research (SLJ and SEZ); and NIH K99/R00 GM114436 (SEZ).
- Antonis Rokas, Reviewing Editor, Vanderbilt University, United States
- Received: February 15, 2017
- Accepted: May 6, 2017
- Version of Record published: June 20, 2017 (version 1)
© 2017, Nuckolls 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.