Repetitive sequences derived from transposons make up a large fraction of eukaryotic genomes and must be silenced to protect genome integrity. Repetitive elements are often found in heterochromatin; however, the roles and interactions of heterochromatin proteins in repeat regulation are poorly understood. Here we show that a diverse set of C. elegans heterochromatin proteins act together with the piRNA and nuclear RNAi pathways to silence repetitive elements and prevent genotoxic stress in the germ line. Mutants in genes encoding HPL-2/HP1, LIN-13, LIN-61, LET-418/Mi-2, and H3K9me2 histone methyltransferase MET-2/SETDB1 also show functionally redundant sterility, increased germline apoptosis, DNA repair defects, and interactions with small RNA pathways. Remarkably, fertility of heterochromatin mutants could be partially restored by inhibiting cep-1/p53, endogenous meiotic double strand breaks, or the expression of MIRAGE1 DNA transposons. Functional redundancy among factors and pathways underlies the importance of safeguarding the genome through multiple means.https://doi.org/10.7554/eLife.21666.001
Heterochromatin, the more tightly packed form of chromatin, plays important roles in maintaining the structural and functional integrity of the genome (Wang et al., 2016). It is less transcriptionally active than euchromatin and highly enriched for repetitive elements such as transposons and satellite repeats, which are kept silent to maintain genome integrity. The heterochromatin state is stable and heritable across generations highlighting the importance of keeping certain regions of the genome repressed.
Histones in heterochromatin are marked with modifications associated with transcriptional repression such as H3K9 methylation. In organisms with point centromeres, heterochromatin is typically found in large domains adjacent to centromeres and telomeres (Wang et al., 2016). In C. elegans, heterochromatin associated histone methylations H3K9me2 and H3K9me3 are instead mostly found in many small domains on the distal arm regions of autosomal chromosomes (Liu et al., 2011). This pattern is likely to be related to the holocentric nature of C. elegans chromosomes, which have distributed centromeres rather than a single point centromere. Two histone methyltransferases carry out all H3K9 methylation (Towbin et al., 2012). The SETDB1 homolog MET-2 carries out mono- and di-methylation of H3K9. SET-25 primarily carries out tri-methylation of H3K9, but it can generate all three methylated forms of H3K9. In the absence of both proteins, H3K9 methylation is undetectable, heterochromatic distal arm regions show reduced association with the nuclear lamina, and heterochromatic transgenes are desilenced (Towbin et al., 2012).
A hallmark of heterochromatin is heterochromatin protein 1 (HP1), the first heterochromatin protein to be discovered through work in Drosophila (Zeng et al., 2010; James and Elgin, 1986). HP1 contains a chromodomain that binds to methylated H3K9, and it is essential for heterochromatin maintenance (Zeng et al., 2010). In addition to HP1, a large and diverse array of proteins is associated with heterochromatin, including nucleosome remodelers, histone modifying enzymes, histone binding proteins, and DNA binding proteins (Saksouk et al., 2015; Meier and Brehm, 2014). However, the functions and interactions of heterochromatin proteins are not well understood.
Many C. elegans proteins that have predicted functions in heterochromatin or transcriptional repression are important for development. These include MET-2/SETDB1, HPL-2/HP1, LIN-61, LIN-13, and LET-418/Mi-2 (8–13). HPL-2 is a C. elegans ortholog of heterochromatin protein HP1, and LIN-61 is a protein containing MBT (malignant brain tumor) repeats. Both HPL-2 and LIN-61 can bind to all methylated forms of H3K9 in vitro (Koester-Eiserfunke and Fischle, 2011; Garrigues et al., 2015; Studencka et al., 2012), and both can repress a heterochromatic reporter (Towbin et al., 2012; Couteau et al., 2002; Harrison et al., 2007). LIN-13 is a multi-zinc finger protein (Meléndez and Greenwald, 2000). A complex containing LIN-13, HPL-2, and LIN-61 has been detected in vivo, and LIN-13 is required for the formation of HPL-2::GFP nuclear foci (Wu et al., 2012; Coustham et al., 2006). LET-418 is an ortholog of Mi-2, an ATP-dependent nucleosome remodelling component of the repressive NuRD and Mec complexes (von Zelewsky et al., 2000; Unhavaithaya et al., 2002; Passannante et al., 2010).
Mutants of hpl-2, lin-61, lin-13, met-2, and let-418 display both germ line and somatic defects. let-418 and lin-13 null mutants are sterile (von Zelewsky et al., 2000; Meléndez and Greenwald, 2000), hpl-2 null mutants show temperature sensitive sterility (Schott et al., 2006), and lin-61 and met-2 null mutants have slightly reduced brood sizes (Koester-Eiserfunke and Fischle, 2011). The underlying cause of the fertility defects is not known, but hpl-2 mutants have been shown to produce abnormal oocytes, suggesting defective gametogenesis (Couteau et al., 2002). Somatic defects are pleiotropic and show similarities among mutants, with most showing slow growth, somatic expression of germ line genes, synthetic vulval development defects, and larval arrest (some only at high temperature) (Meléndez and Greenwald, 2000; Schott et al., 2006; Wu et al., 2012; Harrison et al., 2007; Coustham et al., 2006; Unhavaithaya et al., 2002; Andersen and Horvitz, 2007; Kerr et al., 2014; Petrella et al., 2011; Poulin et al., 2005). Additionally, genetic interactions have been observed between some of the mutants, suggesting partially redundant functions, and that defects may result from alteration of a shared heterochromatin-linked process (Koester-Eiserfunke and Fischle, 2011; Coustham et al., 2006; Simonet et al., 2007).
The genomic distribution of only one of the above heterochromatin proteins has been studied. An HPL-2 ChIP-chip study in early embryos showed that most binding was on the distal arm regions of autosomes in a pattern of similar to H3K9me1 and H3K9me2; interestingly, binding to chromatin was not dependent on H3K9 methylation (Garrigues et al., 2015). HPL-2 was observed to be broadly genic, with additional association at promoters in central chromosome regions and at repeats on distal arm regions; however, no clear relationship between HPL-2 binding and gene expression changes was observed (Garrigues et al., 2015). Systematic and comparative analyses of heterochromatin factors are needed to understand their functions.
The genomic binding patterns of orthologs of some of the above factors suggest roles in the regulation of mobile elements. SETDB1 binds to promoters of developmentally regulated genes in mammalian embryonic stem cells, 40% of which are found next to or overlapping endogenous retroviruses (Yuan et al., 2009; Karimi et al., 2011; Bilodeau et al., 2009). In addition, retrotransposons are derepressed in Setdb1 knockout mouse ES cell lines and primordial germ cells (Karimi et al., 2011; Liu et al., 2014). Retrotransposons are also repressed by HP1α and HP1β in mESCs, but it is a different set of retrotransposons than is targeted by SETDB1 (Maksakova et al., 2013). Drosophila HP1 binds to genes and to transposable elements, particularly in pericentric chromosomal regions, but transposable element expression in mutants has not been assessed (Greil et al., 2003; de Wit et al., 2005). A recent study showed that Mi-2 could bind to a LINE1 retrotransposon promoter and repress a LINE1 reporter in human and mouse cell lines (Montoya-Durango et al., 2016). The genomic distribution of Mi-2 is unclear as different genome-wide binding studies in human ES cells have yielded conflicting results (Hu and Wade, 2012).
The expression of repetitive elements can be detrimental to genome stability due to the negative effects of homologous recombination and transposon-induced breaks. Because the germline produces the gametes that transmit genetic information across generations, silencing of repetitive elements is an absolute requirement for germ line health. A small RNA pathway called the piRNA pathway, present in most animals, plays a role in transposon silencing in the germ line (Weick and Miska, 2014). Recent work in C. elegans implicated HPL-2/HP1 and the H3K9me3 histone methyltransferase SET-25 in piRNA pathway function, indicating a connection between heterochromatin and small RNA silencing of piRNA targets (Ashe et al., 2012).
In the C. elegans germ line, the piRNA pathway involves generation of 21nt piRNAs that bind to the Piwi argonaute protein PRG-1 (Wang and Reinke, 2008; Das et al., 2008; Batista et al., 2008). This triggers generation of secondary 22G siRNAs that mediate silencing either in the cytoplasm or nucleus (Ashe et al., 2012; Das et al., 2008; Shirayama et al., 2012; Luteijn et al., 2012; Lee et al., 2012; Guang et al., 2010; Gu et al., 2009, 2012; Burton et al., 2011; Burkhart et al., 2011; Buckley et al., 2012). Cytoplasmic silencing mechanisms are not well understood, but recent advances have been made in the understanding of transcriptional silencing. In the nucleus, the piRNA pathway engages a second small RNA pathway called the nuclear RNAi pathway (or nrde pathway), which orchestrates H3K9 and H3K27 methylation and/or inhibition of RNA Pol II (Guang et al., 2010; Burkhart et al., 2011; Mao et al., 2015; Alló and Kornblihtt, 2010). Although the nrde pathway can be triggered by the piRNA pathway in the germ line, it is also active in the soma, with dedicated Argonaute proteins for germ line (HRDE-1) and soma (NRDE-3) (Guang et al., 2010; Burkhart et al., 2011; Buckley et al., 2012; Guang et al., 2008). Regions transcriptionally upregulated in hrde-1 mutants were found to be enriched for retrotransposons, suggesting that repetitive elements may be endogenous targets in the germ line (Ni et al., 2014).
In addition to silencing transcription and maintaining the structural and functional integrity of the genome, heterochromatin also plays an important role in DNA repair. Heterochromatic compaction protects DNA from damage, and regulated decondensation is important for damage repair (Feng et al., 2016). Additionally, in mammals, transient formation of heterochromatin occurs at the edges of double strand breaks, which involves recruitment of heterochromatin-associated proteins HP1 and nucleosome remodeller Mi-2, as well as methylation of H3K9 (Gursoy-Yuzugullu et al., 2016). This is thought to aid in damage repair by keeping the broken strands in proximity and inhibiting local transcription.
Here, through systematic genetic and genomic analyses, we investigate interactions and functions of five heterochromatin proteins (HPL-2/HP1, LIN-13, LIN-61, LET-418/Mi-2 and MET-2/SETDB1) and relationships with the piRNA and nuclear RNAi pathways. Our results reveal a nexus of factors that cooperate to prevent expression of repetitive elements and protect the germ line from endogenous damage.
The five genes we study here (hpl-2/HP1, lin-13, lin-61, let-418/Mi-2, and met-2) are needed for normal fertility ([von Zelewsky et al., 2000; Meléndez and Greenwald, 2000; Schott et al., 2006; Koester-Eiserfunke and Fischle, 2011; Ceol et al., 2006; Thomas et al., 2003]; Supplementary file 1). Previous analyses uncovered genetic interactions in fertility between three pairs of genes (hpl-2 and lin-13, lin-61 and hpl-2, lin-61 and met-2; (Koester-Eiserfunke and Fischle, 2011; Coustham et al., 2006; Simonet et al., 2007); however, the remaining six combinations were untested. Using RNAi in mutant backgrounds, we found that double loss of function of each of the uninvestigated pairs also caused synthetic sterility, which we also observed for three tested double mutant combinations (Figure 1A–C). The single mutants show complex and pleiotropic germ line defects, but they all showed a high occurrence of abnormal oocytes, suggesting that sterility may be due in part to abnormal oogenesis (Figure 1—figure supplement 1). The fertility defects of single mutants and the enhancement in double loss of function combinations indicate that the five heterochromatin factors each have unique and partially redundant germ line roles. The genetic interactions suggest that the five factors may cooperate in a germ line process required for fertility.
To begin to investigate the roles of HPL-2, LIN-13, LIN-61, LET-418, and MET-2 in genome regulation, we mapped their binding locations using ChIP-seq analyses in young adults and compared the patterns to each other and to those of H3K9me2 and H3K9me3. Binding of each of the five factors is enriched on the distal arm regions of the autosomes (Figure 2A; Figure 2—figure supplement 1A), as previously seen for H3K9me2, H3K9me3, and HPL-2 (Garrigues et al., 2015; Liu et al., 2011; Sha et al., 2010). Examination of ChIP-seq signals at a more local level revealed similar binding patterns for the five heterochromatin proteins (Figure 2B). Indeed, genome-wide correlation analyses showed significant positive correlations in signal between all datasets (Figure 2—figure supplement 1B). In addition, signals for each of the five heterochromatin factors showed high correlation with H3K9me2 but not with H3K9me3 (Figure 2B, Figure 2—figure supplement 1B).
To further investigate patterns of binding, we identified regions of peak enrichment for each dataset (Figure 2—figure supplement 1C, Figure 2—source data 1; 12449 to 19313 peaks per factor). For each factor, peaks are enriched on the distal chromosomal regions of autosomes; most peaks are intergenic or located in introns, with enrichment for intergenic binding in central chromosomal regions and enrichment for intronic binding in distal arm regions (Figure 2—figure supplement 1A).
To facilitate comparisons between datasets, we merged peak calls from all factors into a superset termed Any5 (n = 33,301), then annotated each region in the Any5 set for the factors bound (Figure 2—source data 1). There is a high degree of peak overlap among the five factors, with 58% of sites in the Any5 set being bound by >1 factor (Figure 2C). Sites uniquely bound by only one factor are in the minority within each dataset (3.4–27.4%, Figure 2C and Figure 2—figure supplement 1C). Strikingly, the largest binding group contains all five factors (termed ‘All5’; Figure 2C). Enrichments for H3K9me2 and H3K9me3 vary between binding classes, with the All5 class showing high enrichment for H3K9me2 (Figure 2C). These results show that HPL-2, LET-418, LIN-13, LIN-61, and MET-2 extensively overlap in binding genome-wide.
The previous HPL-2 ChIP-chip study in embryos noted binding at repetitive elements, which are concentrated on the distal arm regions of autosomes (Garrigues et al., 2015). Repeat-rich heterochromatin in C. elegans is distributed in small domains rather than being concentrated in large regions as in mammals or Drosophila; therefore, the sequences of most repetitive regions have been determined. To investigate the association of heterochromatin factor binding at repetitive DNA, we used the recent Dfam2.0 annotation, which classified 62,331 individual repetitive elements in C. elegans into 184 repeat families, which were further classified by type (e.g., DNA transposon, retrotransposon, satellite, or unknown [Hubley et al., 2016]).
We observed that HPL-2, LIN-13, LIN-61, LET-418, and MET-2 are all strongly associated with repetitive DNA elements (Figure 2C). A large proportion of each factor’s peaks overlaps a repeat sequence (46.3–71.0%), and regions with all five factors have particularly strong repeat association (76.6%, Figure 2C, Figure 2—figure supplement 1C). Furthermore, of the total set of 62331 annotated repetitive elements, nearly half (46%) overlap a peak of at least one factor, and 8002 (13%) overlap all five factors (Figure 2—figure supplement 1D). All repeat types and 180 of 184 repeat families are associated with a heterochromatin factor peak; of these, 105 repeat families are enriched for binding by at least one factor (Figure 2—source data 2). HPL-2, LIN-13, LIN-61, MET-2, and H3K9me2 have a particularly strong association with Helitron families; LET-418 shows generally lower enrichment on repeat families than the other factors (Figure 2D; Figure 2—figure supplements 2–6).
H3K9me2 and H3K9me3 show different patterns of repeat enrichment. H3K9me2 is more associated with DNA transposons and satellite repeats, similar to the heterochromatin factors, whereas H3K9me3 is particularly associated with retrotransposon families, especially LINE and SINE elements (Figure 2D; Figure 2—figure supplements 7–8). We also observed that H3K9me2 and all heterochromatin factors are enriched at telomeres, whereas H3K9me3 is not (Figure 2—figure supplement 1E). The binding and co-association of HPL-2, LET-418, LIN-13, LIN-61, and MET-2 at repetitive elements suggests roles in the regulation of these sequences.
Because silencing of repetitive DNA elements is important for germ line function, we considered that the heterochromatin factors might function in preventing repeat expression. To investigate this possibility, we generated and analysed RNA sequence expression data for wild-type and heterochromatin mutant adults. MET-2 deposits H3K9me1 and H3K9me2, but all three methylation states of H3K9 are still present in met-2 mutants (at lower levels) due to the action of SET-25 (Towbin et al., 2012). Therefore we assayed a met-2 set-25 double mutant, in which H3K9 methylation was not detectable (Towbin et al., 2012). For each strain, we performed two biological replicates and differential expression analyses of the 62,331 Dfam2.0 repeat elements.
We observed upregulation of repetitive elements in every mutant strain (hpl-2, let-418, lin-13, lin-61, and met-2 set-25) (Figure 3A–D, Figure 3—figure supplement 1, Figure 3—source data 1). A total of 71 individual repeat elements representing 29 different families were upregulated in at least one mutant (Figure 3—source data 2; upregulation of 61/71 individual elements was confirmed based on uniquely mapping reads, see Materials and methods). We observed a striking overlap in the sets of repetitive elements regulated by the heterochromatin factors: 41% of elements are upregulated in more than one mutant (Figure 3A; Figure 3—source data 2). Furthermore, seven repeat elements are upregulated in all five strains, all of which are MIRAGE1 DNA transposable elements (Figure 3A,C,D, Figure 3—source data 2). The majority of repetitive elements upregulated in each heterochromatin mutant strain are DNA transposons, but retrotransposons are enriched for being upregulated (Figure 3B). Mutants show variation in the classes of repeats regulated; for example, SINE retrotransposons are particularly affected in let-418 mutants, while many Helitron elements are upregulated in lin-13 mutants (Figure 3B).
Overall, the total number of individual repetitive elements found with significantly altered expression is extremely small (<1%) relative to the >30,000 with factor binding, indicating that binding does not generally regulate repeat transcription. There are many types of repetitive elements, and only a small fraction would be expected to have potential for RNA expression. For example, 67% of repetitive elements are predicted to be non-autonomous DNA transposons, which would be mobilised in trans by a transposase encoded by another repetitive element, and many annotated elements are small fragments of larger elements. We therefore wondered whether the upregulation of repetitive element expression in heterochromatin mutants might be particularly associated with transposases or retrotransposons. Of 62331 Dfam2.0 elements, 221 overlap a predicted transposase ORF, and 1085 are annotated as LTR retrotransposons. We found that elements upregulated in any heterochromatin factor mutant are 83-fold enriched for containing a transposase (21 of 71) and 10-fold enriched for LTR retrotransposons (13 of 71), together accounting for nearly half of upregulated repeats. Therefore, a key role of heterochromatin factors is to suppress expression of repetitive element transposases. The widespread binding of heterochromatin factors to non-expressed repetitive elements is likely to play roles other than in the regulation of transcription. These could include preventing the cutting, copying, or movement of elements, or maintaining genome integrity by supressing homologous recombination between repetitive elements (Chiolo et al., 2011; Sinha et al., 2009).
We also analysed alterations in protein coding gene expression in the heterochromatin mutants. Consistent with roles in repression, we identified three to five times more genes with upregulated expression in each mutant strain compared to those with reduced expression (267–513 upregulated genes per mutant; Figure 3—source data 3). Additionally, there is a high degree of overlap among the upregulated genes; of the total set of 1155 genes upregulated in any of the five mutant strains, 404 are upregulated in more than one (Figure 3—source data 3). Heterochromatin factors are enriched at upregulated genes, but not downregulated genes (except for genes misregulated in let-418 mutants); additionally, both H3K9me2 and H3K9me3 are enriched at upregulated genes in all mutant strains (Figure 3—figure supplement 2). Enrichment for all factors and H3K9 methylation is particularly strong at genes upregulated in met-2 set-25 mutants (Figure 3—figure supplement 2). These associations suggest direct roles in repression.
The silencing of repetitive elements is a universal conserved feature of germ line function. The prominent upregulation of MIRAGE1 elements in all heterochromatin mutants prompted us to ask whether expression of this element might play a role in their reduced fertility. MIRAGE1 is an autonomous DNA transposable element that has two open reading frames. Of 69 MIRAGE1 element annotations in Dfam2.0, only six are full length. These six, plus an additional six partial MIRAGE1 elements are upregulated in at least one heterochromatin mutant, and both ORFs show upregulation.
We first examined the tissue distribution of MIRAGE RNA using RNA-FISH (Raj et al., 2008). As expected from the RNA-seq results, wild-type adults had very low levels of MIRAGE1 RNA-FISH signal in germ line and soma (Figure 3E and Figure 3—figure supplement 3). In three tested heterochromatin mutants (hpl-2, let-418, and lin-13), we observed abundant germ line localized MIRAGE1 RNA whereas somatic expression remained low (Figure 3E and Figure 3—figure supplement 3). Therefore, hpl-2, let-418, and lin-13 are important for repression of MIRAGE1 in the germ line.
To test whether upregulation of MIRAGE1 contributes to sterility, we used two sets of RNAi clones to simultaneously knockdown ORF1 and ORF2 (sets termed mirage-A and mirage-B). mirage-A and mirage-B target 16 different MIRAGE1 elements, including all full length elements and most of the MIRAGE1 elements upregulated in each of these mutants (8/8 for let-418, 7/8 for lin-13, and 10/11 for hpl-2). To assess an effect on fertility, we grew hpl-2, lin-13, and let-418 mutants at 25°C, a condition under which they are nearly sterile, and tested for an increase in brood size after RNAi knockdown. Remarkably, RNAi of MIRAGE1 using mirage-A or mirage-B sets of RNAi clones led to a small but significant increase in fertility of all three mutants, showing that inappropriate MIRAGE1 expression contributes to their sterility (Figure 4A). We also observed that MIRAGE1 RNAi resulted in amelioration of somatic growth defects (not shown). These results indicate that one mechanism by which heterochromatin proteins promote normal germ line function is via the repression of repetitive elements, in particular those encoding transposases.
Desilencing of repetitive elements has been reported to cause DNA damage in other organisms (Wallace et al., 2013); therefore, repeat expression in heterochromatin mutants might lead to genotoxic stress and genome instability in the germ line. Consistent with this, loss of lin-61 leads to replication stress and genome instability, with increased germ line and somatic mutation frequency (Johnson et al., 2013; Pothof et al., 2003). lin-61 mutants also have defects in DNA repair (Johnson et al., 2013; Pothof et al., 2003). A previous study reported that an hpl-2(tm1489) null mutant strain was hypersensitive to ionizing radiation (IR) (Luijsterburg et al., 2009); however, we found that this strain also harboured a deletion in the polq-1 gene, which encodes DNA polymerase theta. Because polq-1 mutants are reported to have increased sensitivity to DNA damaging agents and display genome instability (Muzzini et al., 2008), it was unclear if the defects observed were due to hpl-2 (see Materials and methods).
To determine whether hpl-2 has a role in DNA repair, we tested the response of the isolated hpl-2(tm1489) mutant to IR induced DNA damage. Following IR, we observed that hpl-2 mutants show higher levels of oocyte fragmentation compared to wild type, suggesting that they are defective in DNA repair (Figure 5—figure supplement 1). Additionally, hpl-2 mutant germ lines are hypersensitive to induction of phosphorylation of the DNA damage checkpoint kinase CHK-1 (Figure 5—figure supplement 1). The hypersensitivity of hpl-2 and lin-61 mutants to exogenous DNA damage are consistent with increased genotoxic stress in the germ line.
We considered that the repeat desilencing and DNA repair defects of heterochromatin mutants might lead to increased germ line apoptosis, and thereby contribute to germ line and fertility defects. In wild-type animals, physiological apoptosis occurs in the pachytene region of the gonad, with around half of the initially produced germ cells eliminated by apoptosis as a quality control mechanism (Gartner et al., 2008). DNA damage causes increased apoptosis over physiological levels, and this increase is dependent on cep-1/p53 (Schumacher et al., 2001; Derry et al., 2001). To assess germ line cell death in the heterochromatin mutants we used a CED-1::GFP reporter, which allows visualization of apoptotic germ cells in adult animals (Zhou et al., 2001). We observed that hpl-2, lin-13, lin-61, and set-25 met-2 mutants all displayed increased germ line apoptosis (Figure 5; let-418 was not assayed because the apoptosis reporter used is genetically linked). Thus, heterochromatin factor mutants have increased germ cell death.
p53 is important for transduction of the DNA damage response and other stresses, and C. elegans cep-1/p53 is required for damage induced cell death (Schumacher et al., 2001; Derry et al., 2001). We used RNAi to test whether activation of p53 dependent pathways played a role in heterochromatin mutant sterility. Following RNAi of cep-1/p53, we found that the brood sizes of hpl-2, lin-13, and let-418 mutants grown at 25°C were modestly increased (Figure 4A). We further tested the effect of loss of cep-1 by making double mutants with cep-1(lg12501). Similar to the RNAi results, we observed that mutation of cep-1 increased the fertility of lin-13, let-418 and hpl-2 mutants (Figure 4B). This increase is not due to a general effect of cep-1 on fertility, as cep-1 mutants have a slightly reduced brood size compared to wild-type animals (Figure 4B). We also observed that cep-1 loss partially rescued the slow growth phenotype of the mutants (Figure 4C). These results suggest that genotoxic stress and DNA damage signalling in heterochromatin mutants activates p53, which contributes to sterility and slow growth. The increase in fertility upon cep-1/p53 inhibition may be a direct consequence of reduced germ line apoptosis, or alternatively the effect may be indirect, by preventing DNA damage signalling or improving growth rate. We also note that although fertility of heterochromatin mutants is increased when cep-1/p53 is inhibited, it is not restored to wild-type levels indicating that other mechanisms contribute to sterility.
We next investigated whether endogenous physiological DNA damage may also contribute to heterochromatin mutant sterility. During meiosis, double strand breaks are induced by the topoisomerase-like protein SPO-11 to facilitate crossover formation and meiotic recombination (Dernburg et al., 1998). Similar to inhibition of damage induced cell death or MIRAGE1 expression, we found that inhibiting meiotic double strand breaks by RNAi of spo-11 increased the brood size of hpl-2, lin-13, and let-418 mutants (Figure 4A), suggesting that defects in repair of meiotic double strand breaks contributes to sterility.
The piRNA pathway has a well-known role in preventing the activity of transposons in the germ line (Weick and Miska, 2014). In C. elegans, the piRNA pathway operates through the Piwi Argonaut protein PRG-1. Silencing occurs both transcriptionally, through engagement of the nuclear RNAi pathway, and post-transcriptionally, through a poorly understood mechanism. Interestingly, prg-1 mutants have fertility defects, displaying a low brood size and a mortal germline phenotype that is more pronounced at elevated temperatures (Das et al., 2008; Batista et al., 2008). The observation that heterochromatin mutants desilence repetitive elements together with the finding that HPL-2 and H3K9 methyltransferse SET-25 are needed for piRNA pathway function in conjunction with the nuclear RNAi pathway (Ashe et al., 2012) prompted us to further investigate connections between these factors.
We first assayed the expression of repetitive DNA in prg-1 mutant adults because genome-wide profiling had not previously been done. We detected upregulation of 18 repetitive elements in prg-1 mutants, 14 of which are also upregulated in at least one of the heterochromatin mutants, including MIRAGE1 elements (Figure 6A, Figure 3—source data 1 and 2). RNA FISH experiments showed that MIRAGE1 RNA is increased in prg-1 mutant germ lines, similar to observations in heterochromatin mutants described above (Figure 3E and Figure 3—figure supplement 3). Given this overlap in targets and the fertility defects of prg-1 mutants, we assessed whether they also showed increased germ line apoptosis as seen in heterochromatin factor mutants. Indeed, we observed significantly increased germ cell death in prg-1 mutant adults (Figure 6B). Therefore, the piRNA pathway and heterochromatin factors have shared targets and phenotypes, and likely collaborate in maintaining genomic integrity of the developing germline.
We next used a piRNA activity sensor to test whether heterochromatin factors other than hpl-2 are needed for piRNA pathway function. Similar to hpl-2 and set-25, we found that lin-61 and let-418 mutants derepress the piRNA sensor reporter (Figure 6C,D). We also observed weak desilencing in a fraction of met-2 mutants (Figure 6D), which was not observed in a previous assay (Ashe et al., 2012). However, the piRNA sensor was not desilenced in lin-13 mutants. It is possible that the lack of desilencing is due to the lin-13(n770) allele being non-null, however this mutant does show defects such as upregulation of repetitive elements and increased apoptosis.
A previous study profiling small RNAs in hpl-2 mutants in a piRNA sensor background showed that piRNAs targeting the sensor or a few endogenous targets were not altered in abundance, suggesting that hpl-2 acts downstream of piRNA production (Ashe et al., 2012). To investigate this further, we compared the global abundance of piRNAs in hpl-2 and wild-type adults. Similar to the above results, we found that hpl-2 mutants make normal levels of piRNAs (Figure 6—figure supplement 1). We also investigated the production of secondary 22G siRNAs in hpl-2 mutants. We detected a decrease in 22G RNAs mapping near predicted piRNA target sites in prg-1 mutants as previously observed (Lee et al., 2012), but levels were normal in hpl-2 mutants (Figure 6—figure supplement 1). hpl-2 mutants also showed normal levels of 22Gs at repeat elements. (Figure 6—figure supplement 1). Therefore, at least for hpl-2, the role in the piRNA pathway appears to be downstream of piRNA and subsequent 22G RNA synthesis.
To summarize, hpl-2, lin-61, let-418, set-25, and met-2 are important for piRNA pathway function. Nevertheless, the widespread binding sites and desilencing of additional targets relative to prg-1 indicate that heterochromatin proteins also mediate repression that is not piRNA-induced.
The C. elegans nuclear RNAi pathway (called the nrde pathway) mediates transcriptional repression and directs H3K9me3 methylation to its targets (Guang et al., 2010; Gu et al., 2012; Burton et al., 2011; Burkhart et al., 2011; Buckley et al., 2012; Guang et al., 2008). The nrde pathway also functions in repression of piRNA targets (Ashe et al., 2012). To investigate the relationship between the nrde pathway, the piRNA pathway, and heterochromatin factors in repetitive element regulation, we carried out RNA-seq on nrde-2(gg91), a putative null mutant, and compared results to those of heterochromatin and prg-1 mutants. We observed that nrde-2 mutants showed a larger and different spectrum of repetitive element desilencing compared to prg-1 or any of the heterochromatin mutants (Figure 7—figure supplement 1, Figure 3—source data 1 and 2). Of 71 elements desilenced in nrde-2 mutants, only seven overlap a repeat desilenced in one of the heterochromatin mutant strains (Figure 7—figure supplement 1). Notably MIRAGE1 elements, prominently upregulated in heterochromatin and prg-1 mutants, are not desilenced in nrde-2 mutants (Figure 3—source data 1 and 2; Figure 7—figure supplement 1). Retrotransposons are highly enriched among nrde-2 targets (45/71) whereas heterochromatin factors and prg-1 are more associated with DNA transposon misregulation (Figure 3B). Therefore, although the nrde pathway is required for aspects of piRNA function, repetitive element targets largely differ. Notably, the finding that elements derepressed in nrde-2 mutants differ from those in met-2 set-25 mutants, which lack detectable H3K9 methylation, suggests that H3K9 methylation may not be required for nrde dependent repression.
Like the heterochromatin factor and prg-1 mutants, nrde-2 mutants also show a temperature sensitive decrease in fertility (Guang et al., 2010). To test whether the nrde-2 fertility function had functional overlap with heterochromatin factors, we constructed double mutants between nrde-2 and three mutants (hpl-2, lin-61, and let-418). We observed no reduction in fertility for nrde-2; hpl-2, and a weak but non-significant reduction for nrde-2; lin-61 double mutants (Figure 7A). However, nrde-2; let-418, double mutants showed a significantly smaller brood size than expected compared to the single mutants, indicating partial functional redundancy between let-418 and the nrde pathway (Figure 7A). We also observed that all three double mutants showed significantly increased embryo lethality compared to the single mutants (Figure 7B).
To further investigate the genetic interaction between nrde-2 and let-418, we carried out RNA-seq of nrde-2; let-418 adults to test for redundancy in repeat element repression. We found that more repeats are upregulated in nrde-2; let-418 double mutants compared to nrde-2 or let-418 single mutants (Figure 7B). Most of the repeat elements upregulated only in the nrde-2; let-418 double mutant are retrotransposons (27/46; Figure 7B and Figure 3—source data 2). We conclude that NRDE-2 and LET-418 have unique and redundant roles in the repression of repetitive DNA elements.
Because a key output of the nrde pathway is the deposition of H3K9me3, the observed redundancy between NRDE-2 and LET-418 prompted us to investigate whether the nrde pathway might control H3K9me3 levels at heterochromatin regulated loci. To this end, we used published H3K9me3 ChIP-seq datasets in four different nrde mutants (hrde-1, nrde-2, nrde-3, and nrde-4; (Gu et al., 2012; Buckley et al., 2012; Ni et al., 2014). and analysed levels at genes and repeats upregulated in nrde-2 mutants or only in heterochromatin mutants. The nrde pathway acts in the germ line and soma: HRDE-1 and NRDE-3 are argonautes specific for germ line or soma, respectively, whereas NRDE-2 and NRDE-4 act in all tissues (Guang et al., 2010; Burkhart et al., 2011; Buckley et al., 2012; Guang et al., 2008). We observed that repeat elements and genes upregulated in nrde-2 mutants also have reduced H3K9me3 levels, supporting the link between H3K9me3 methylation and repression of endogenous targets (Figure 7—figure supplements 2 and 3). H3K9me3 was also reduced on nrde-2 upregulated elements in mutants of other nrde genes that act in the germ line (hrde-1 and nrde-4), but not in the soma specific argonaute mutant nrde-3 (Figure 7—figure supplements 2 and 3). This suggests that the transcriptional upregulation observed in nrde-2 mutants occurs largely in the germ line.
We next analysed H3K9me3 levels in sets of genes and repeats upregulated in heterochromatin mutant strains but not in nrde-2 mutants to ask if these elements were also under nrde control. Indeed, genes upregulated in any of the five heterochromatin factor mutant strains (hpl-2, lin-13, let-418, lin-61, met-2 set-25) but not in nrde-2 mutants also showed reduced H3K9me3 in germ line nrde mutants, though the reduction was weaker than for nrde-2 regulated genes (Figure 7—figure supplement 3). Repeats upregulated only in heterochromatin factor mutants showed a trend of reduced H3K9me3 (Figure 7—figure supplement 2). Therefore, the germ line nuclear RNAi pathway partially controls H3K9me3 levels at loci regulated by heterochromatin factors. Because these elements are not upregulated in nrde-2 mutants, this indicates that the observed reduction of H3K9me3 is not sufficient for derepression and supports partial redundancy between the nrde pathway and heterochromatin factors in repeat silencing.
All animal genomes contain abundant repetitive elements, which are subject to silencing control. This study expands our knowledge of repetitive element silencing by showing that a diverse set of heterochromatin factors (HPL-2/HP1, LIN-61, LET-418/Mi-2, LIN-13, and MET-2) work together with the piRNA and nuclear RNAi pathways to silence repetitive elements such as DNA transposons and retrotransposons. The systematic analyses of multiple factors, most of which are conserved, uncovered a network of functional interactions between them. We suggest that the interactions we identify here are likely to be relevant to the control of repetitive elements in other animals.
All factors and pathways studied are individually important for germ line function, as evidenced by reduced fertility or sterility of single mutants, and all are individually necessary for repetitive element silencing. Importantly, functional redundancy among the factors and pathways demonstrates widespread safeguards for ensuring germ line health and fertility. Our results show that there are interacting and overlapping mechanisms of repeat element silencing (Figure 8A).
Connections between heterochromatin formation and transcriptional silencing via RNAi mechanisms involving small RNAs have been observed in a variety of organisms (Castel and Martienssen, 2013; Holoch and Moazed, 2015; Martienssen and Moazed, 2015). For instance, RNAi machinery directs silencing at repetitive centromeric regions in S. pombe in a process that involves H3K9 methylation and the chromodomain protein Swi6, which is similar to HP1 (Holoch and Moazed, 2015; Hayashi et al., 2012; Motamedi et al., 2008; Rougemaille et al., 2012). A second S. pombe HP1 homolog, Chp2, functions in transcriptional repression in heterochromatin downstream of the RNAi factors via a complex called SHREC2, which contains Mit2, an Mi-2 related protein (Holoch and Moazed, 2015; Motamedi et al., 2008). These two HP1 homologs each make partial contributions to silencing, since swi6 chp2 double mutant cells have a stronger silencing defect than either single mutant, suggesting partial redundancy in the two processes (Motamedi et al., 2008). Nuclear pathways involving small RNAs, H3K9 methylation, HP1 homologs and/or Mi-2 proteins also repress repetitive elements and genes in different eukaryotes including Arabidopsis, Drosophila, mouse, and humans (Castel and Martienssen, 2013; Holoch and Moazed, 2015; Martienssen and Moazed, 2015; Friedli and Trono, 2015; Iwasaki et al., 2015). However, the mechanisms linking silencing pathways are not fully understood and factors involved in heterochromatin formation and function remain to be identified. For example, a recent study of HP1a interactors in Drosophila identified many new proteins needed for gene silencing and/or heterochromatin organization (Swenson et al., 2016).
Previous studies in C. elegans have also uncovered connections between heterochromatin factors and small RNA pathways. The piRNA pathway is a small RNA pathway active in the germ line that silences transposons and genes through cytoplasmic and nuclear mechanisms (Weick and Miska, 2014). In the nucleus, the piRNA pathway engages the nrde pathway and heterochromatin factors for transcriptional repression: HPL-2, the H3K9me3 histone methyltransferase SET-25, and nuclear RNAi factors are necessary for silencing a piRNA pathway sensor (Ashe et al., 2012). The nrde pathway directs H3K9me3 both endogenously and in response to exogenous dsRNA and effects transcriptional repression in both the germ line and soma (Guang et al., 2010; Gu et al., 2012; Burkhart et al., 2011; Guang et al., 2008). Endogenous germ line nrde targets have been suggested to include retrotransposons based on their enrichment within genomic intervals that display increased expression and decreased H3K9me3 levels in germ line nuclear RNAi mutants (Ni et al., 2014). Here, through genetic and profiling analyses, we have established additional connections between heterochromatin factors and small RNA pathways, linking them to repetitive element repression, uncovering functional redundancy, and expanding understanding of their relationships.
We found that the genome-wide distributions of each of the five heterochromatin factors studied here (HPL-2/HP1, LIN-13, LIN-61, LET-418/Mi-2, and MET-2/SETDB1) are highly correlated with each other and strongly associated with repetitive elements. These patterns are correlated with H3K9me2, but not with H3K9me3, as previously seen for HPL-2 in embryos (Garrigues et al., 2015). H3K9me2 and H3K9me3 modifications largely do not overlap (this study and [Liu et al., 2011]), but both are associated with repetitive elements. We further found that H3K9me2, but not H3K9me3 is enriched at telomeres. These patterns support functional differences between H3K9me2 and H3K9me3.
In addition to the similarity in binding profiles, we found that hpl-2, lin-13, lin-61, let-418, and met-2 set-25 mutant strains all showed derepression of repetitive elements and genes. While this paper was under review, Zeller et al reported that met-2 set-25 mutants derepressed transposable element expression in embryos and gonads, similar to the results presented here for met-2 set-25 young adults (Zeller et al., 2016). The global loss of H3K9 methylation also leads to transposon derepression and mobilization in Drosophila (Penke et al., 2016). The patterns of upregulated repetitive elements and genes among the five heterochromatin mutant strains are strikingly similar, indicating shared targets. However, although binding profiles and consequences of loss are similar, the factors also have unique roles. Furthermore, genetic interactions between all pairs show that they have partially redundant functions. To understand these relationships, it will be important to investigate their interdependencies and the consequences of inactivating multiple factors together.
Comparing expression profiles of heterochromatin mutants to those of prg-1 (piRNA pathway) and nrde-2 (nuclear RNAi pathway) mutants, we observed that repeat elements and genes have similar patterns of derepression in heterochromatin factor and prg-1 mutants, but these largely differ from those in nrde-2 mutants. Consistent with a functional link between the heterochromatin factors and the piRNA pathway, a previous study showed that HPL-2 and SET-25 are needed for piRNA pathway function (Ashe et al., 2012). Here we further found that LIN-61, LET-418, and MET-2 (weakly) are also important. It appears that heterochromatin proteins act as downstream effectors of the piRNA pathway rather than having a role in small RNA biogenesis or stability since levels of piRNAs and their secondary 22G RNAs are normal in hpl-2 mutants (Ashe et al., 2012) (and this study). Investigating whether small RNA populations are altered in other heterochromatin mutants will be needed to confirm this hypothesis. This mechanism appears to differ from the situation in S. pombe, where H3K9 methylation and the chromodomain protein Swi6 are required for the association of silencing complexes that generate siRNAs (Holoch and Moazed, 2015; Martienssen and Moazed, 2015; Motamedi et al., 2008, 2004; Verdel et al., 2004). However, it is possible that redundancy between heterochromatin factors in C. elegans may have masked involvement in small RNA production.
Many more elements are desilenced in nrde-2 mutants than in prg-1 mutants, with little overlap between the two. The elements derepressed in nrde-2 mutants are mostly LTR retrotransposons, in line with a study finding transcriptionally upregulated genomic intervals in hrde-1 mutants to be enriched for LTRs and unaffected in prg-1 mutants (Ni et al., 2014). The apparent difference in targets between NRDE-2 and PRG-1 could be due to the requirement for PRG-1 in initiation but not maintenance of silencing. Once silencing is established by PRG-1, nuclear RNAi maintains silencing in a process termed RNAe that depends on continued generation of secondary siRNAs by mutator proteins, the presence of secondary siRNA-associated argonautes (including nrde-2), and maintenance of the established chromatin state by heterochromatin factors (Ashe et al., 2012; Shirayama et al., 2012; Luteijn et al., 2012; Lee et al., 2012; de Albuquerque et al., 2015).
Our study also uncovered interactions between heterochromatin factors and the nuclear RNAi pathway. We found that let-418; nrde-2 double mutants show a strongly enhanced fertility defect compared to the single mutants, and that they desilence a larger set and a wider spectrum of repetitive elements. Therefore, for some elements, either LET-418 or NRDE-2 is sufficient for silencing, demonstrating redundancy in repetitive element silencing. These interactions further emphasize the overlapping safeguards that function to effectively repress repetitive elements. The increased embryo lethality seen in double mutants between nrde-2 and three tested heterochromatin factors (hpl-2, lin-61, or let-418) suggest additional as yet unexplored redundancy between the nuclear RNAi pathway and heterochromatin factors. That a substantial number of repetitive elements are desilenced in heterochromatin factor mutants but not in prg-1 or nrde-2 mutants suggests that heterochromatin factors can also act as independent agents, silencing repetitive elements independently of small RNA pathways.
Interestingly, genes and repeats upregulated in nrde-2 mutants more often have high levels of H3K9me3 than H3K9me2 whereas those upregulated in met-2 set-25 mutants (which lack all H3K9 methylation) show the opposite pattern and more often have high H3K9me2 marking (Figure 3—figure supplement 2). The association between H3K9me3 and nrde-2 upregulated genes suggests that the nuclear RNAi pathway may specifically engage this modification. Consistent with this, repeats and genes upregulated in nrde-2 mutants have strongly reduced H3K9me3 levels in germ line nuclear RNAi pathway mutants. However, the difference in elements desilenced in nrde-2 and met-2 set-25 mutants (which lack H3K9 methylation) argues against an essential requirement for H3K9 methylation in nrde mediated repression. We observed that H3K9me3 levels in nrde-2 and other germline nuclear RNAi mutants are also weakly reduced at genes and repeats repressed by heterochromatin pathway factors, even though these elements are not upregulated in nrde-2 mutants. This suggests that the heterochromatin factors and the nuclear RNAi pathway may regulate many common elements, but that heterochromatin factors can still effectively silence them in the absence of the nuclear RNAi pathway. Future analyses in mutants compromised for both nuclear RNAi and heterochromatin factors will be needed to address the mechanisms of this redundancy.
We speculate that in many cases, repetitive element regulation involves a local mechanism rather than the spreading of large heterochromatin domains. First, we observe that heterochromatin factor binding is often closely associated with repetitive elements and does not extend to adjacent genes. Second, genes containing repetitive elements bound by heterochromatin factors (usually within introns) are often expressed. Indeed, one fourth of genes contain a repetitive element bound by a heterochromatin factor, and of those, 59% (3287/5568) are expressed in the germ line. Formation of a large inactive heterochromatin domain would clearly be incompatible with such widespread germ line expression.
In C. elegans, most H3K9 marking occurs on the distal chromosome arms, where small regions of H3K9 are interspersed with chromatin typical of euchromatin (Liu et al., 2011). Many active genes, including those expressed in the germ line, reside in these arm regions (Liu et al., 2011). Intriguingly, the repeat- and H3K9-rich chromosome arms are generally associated with the nuclear lamina, a region implicated in transcriptional repression (Towbin et al., 2012; Ikegami et al., 2010). Active genes at the periphery that contain repetitive elements bound by heterochromatin factors may be subject to special mechanisms for their expression.
In addition to functioning in repetitive element repression, some of the heterochromatin factors we studied here are implicated in DNA repair or genome stability. We found that hpl-2 mutant germ lines show reduced repair and increased activation of DNA damage signaling in response to ionizing radiation. LIN-61 is needed for DNA repair in the germ line and its loss causes an increase in the germ line mutation rate (Johnson et al., 2013; Pothof et al., 2003). Additionally, both lin-61 and set-25 were identified in a genome-wide RNAi screen for genes needed for genome stability in the soma (Pothof et al., 2003). Furthermore, met-2 set-25 mutants, which lack all H3K9methylation, were recently shown to have increased sensitivity to replication stress and increased rates of repeat associated mutations and R loops (Zeller et al., 2016). In mammalian cells, orthologs of LET-418 (Mi-2), HPL-2 (HP1), and MET-2 (SETDB1), have documented roles in DNA repair (Alagoz et al., 2015; Polo et al., 2010; Urquhart et al., 2011). Mi-2 is needed for recruitment of DNA repair proteins to sites of DSBs, and loss of Mi-2 from human fibroblast cell lines leads to apoptosis and sensitivity to ionizing radiation (Larsen et al., 2010; Pan et al., 2012; Smeenk et al., 2010). HP1 accumulates at DSBs and its depletion causes abnormal recruitment of repair factors (Soria and Almouzni, 2013). Additionally, DNA damage repair defects caused by depletion of SETDB1 are similar to those seen upon loss of HP1 (Alagoz et al., 2015). Defects in repair of DNA lesions are likely to cause germ line stress and to contribute to the germ line instability, germ line development defects, and increased germ line apoptosis seen in heterochromatin factor mutants. Such processes might also underlie the reduced fertility and increased germ line apoptosis seen in prg-1 mutants.
The activation of MIRAGE1 DNA transposases in all heterochromatin factor mutant strains and prg-1 mutants would be expected to cause double strand breaks and/or replication stress. We show that this abnormal expression contributes to sterility because fertility was partially restored in hpl-2, let-418, and lin-13 mutants when MIRAGE1 transcripts were knocked down via RNAi. Similarly, inhibiting endogenous meiotic double strand breaks by knockdown of spo-11 also partially restored fertility. These results suggest that heterochromatin factors act to combat different types of genotoxic insults, both through silencing repetitive elements and facilitating repair. If not dealt with, these insults cause sterility (Figure 8B).
We also observed that loss of cep-1/p53 suppressed heterochromatin factor defects. p53 is important for mediating DNA damage signaling (Meek, 2009). In C. elegans, p53/cep-1 is required for damage induced germ cell death (Schumacher et al., 2001; Derry et al., 2001). In the soma, DNA damage signaling does not lead to p53/CEP-1-mediated apoptosis; however, CEP-1 does play a role in DNA repair in the soma, and it slows larval development in response to loss of CLK-2/TEL2 DNA damage signaling (Derry et al., 2007; Hoffman et al., 2014). Our findings that loss of cep-1 partially suppresses the sterility and slow growth phenotypes of hpl-2, lin-13, and let-418 suggests that damage signaling and cep-1/p53 underlies these defects.
Interestingly, none of the heterochromatin mutant strains studied here display hallmarks of mutators such as high embryo lethality or the frequent production of progeny with visible mutant phenotypes. We propose that quality control mechanisms in the germ lines of heterochromatin factor mutants largely prevent improperly repaired meiotic germ cells from becoming mature gametes, either through apoptosis or the arrest of gametogenesis, to ensure that mutation rates are low.
This study indicates a complex orchestration of fertility protection by HPL-2/HP1, LIN-13, LIN-61, MET-2, and LET-418/Mi-2 together with the piRNA and nuclear RNAi pathways. Repression of repetitive elements may prevent replication stress and DNA damage, but when damage does occur, these heterochromatin proteins participate in repair pathways to maintain genome integrity. Further work will be required to untangle the mechanisms and individual roles in DNA repair pathways and repetitive element repression.
Strains were cultured using standard methods (Brenner, 1974). Strains used in the paper are given in Supplementary file 2. Whole genome sequencing of PFR40 hpl-2(tm1489) identified an 882 bp deletion in the polq-1 gene at chrIII:5792238–5793119. The underlined T residue marks the junction of the deletion and matches the flanking sequence of both sides of the deletion: TAAATCTCTATCCGATGTGATCCACGTCGATAACATTATTC; we have named this lesion polq-1(we100). The JA1902 strain harboring hpl-2(tm1489) but lacking polq-1(we100) was derived by outcrossing MT15062 hpl-2(tm1489);hpl-1(n4317), which does not contain polq-1(we100).
Wild-type young adults (YA) were prepared by growing synchronized L1s in liquid culture using standard S-basal medium with HB101 E. coli for 60 hr at 20°C. Adults were sucrose floated, washed in PBS, and flash frozen in liquid nitrogen. Extract preparation and chromatin immunoprecipitation were performed as in Kolasinska-Zwierz et al. (2009) with the following modifications: tissue was fixed for 10 min in 1.5 mM EGS (Pierce 21565) then formaldehyde added to 1% for a further 10 min before quenching with 0.125M glycine and washing 2X with PBS plus protease inhibitors. Pellets were washed once in FA buffer, then resuspended in 1 ml FA buffer per 1 mL of ground worm powder and the extract sonicated to an average size of 250 base pairs with a Diagenode Bioruptor or Bioruptor Pico for 28 pulses of 30 s followed by 30 s pause. Antibodies used for ChIP are given in Supplementary file 3. Following ChIP and DNA purification, libraries were prepared using the Illumina TruSeq kit. Fragments in the 250–300 base pair range were selected using Agencourt AMPure XP beads. Two biological replicate ChIPs were conducted for each factor.
Synchronized, starved L1 stage worms were grown on NGM plates under one of two conditions. Condition 1 (hpl-2, let-418, lin-61, met-2 set-25, and N2): growth was at 20°C until the L4 stage and then worms were shifted to 25°C for 15–18 hr until they reached young adult stage. Condition 2 (lin-13, prg-1, nrde-2, nrde-2; let-418, and N2): growth was at 15°C until the L4 stage and then worms were shifted to 25°C for 15–18 hr until they reached young adult stage. Worms were then harvested, flash frozen in liquid nitrogen, and stored at −80°C until use. RNA was extracted from frozen worms using TriPure (Roche). RNA was purified with Zymo Research RNA Clean and Concentrator-5 (Cambridge Bioscience) following DNAse I digestion. Ribosomal RNA was depleted using Ribo-Zero rRNA Removal Kit (Human/Mouse/Rat) (Illumina). Libraries were prepared using the NEBNext Ultra Directional RNA Library Prep Kit for Illumina (New England Biolabs). Two biological replicates were prepared for each strain.
ChIP-seq and RNA-seq libraries were sequenced using Illumina HiSeq. Reads were aligned to the WS220/ce10 assembly of the C. elegans genome using BWA v. 0.7.7 ( Li and Durbin, 2010) with default settings (BWA-backtrack algorithm). The SAMtools v. 0.1.19 ‘view’ utility was used to convert the alignments to BAM format. To be able to investigate binding and expression at repetitive elements, we used all aligned reads (mapq0) to generate pileup and normalised tracks. Normalized ChIP-seq coverage tracks were generated using the BEADS algorithm (Cheung et al., 2011) without the mappability correction step. ChIP-seq and RNA-seq library read numbers and alignment statistics are given in Figure 2—source data 3.
Broad and sharp ChIP-seq peaks were generated as follows. Initial ChIP-seq peaks were called using MACS v. 2.1.1 (Feng et al., 2012) with a permissive 0.7 q-value cutoff and fragment size of 150 bp against a summed ChIP-seq input. These were used in conjunction with a modified IDR procedure to generate broad peak calls ([Li et al., 2011]; https://www.encodeproject.org/software/idr/) with an IDR threshold of 0.05 to combine replicates. These broad peaks are termed ‘IDR peaks’ (Figure 2—source data 1). The pipeline for generating IDR peaks is available here: https://github.com/Przemol/biokludge/blob/master/macs2_idr/macs2_idr.ipy. To generate sharp peak calls, the IDR calls were further refined using an adhoc post-processing step, as visually distinct peaks close to each other were often contained within single broad peaks. We identified concave regions within the IDR peaks using the smoothed second derivative of the mapq0 pileup coverage signal with 250 bp kernel (https://github.com/Przemol/biokludge/blob/master/macs2_idr/concave_regions.py). We empirically found the minimum of the second derivative within a concave region to be a good indicator of a visually compelling peak, and used concave regions (within IDR peaks) with a threshold of lower than −500 curvature index. Next, we discarded peaks with MASC2 score lower than 100 and peak width lower than 100 bp. The resulting peaks were filtered against combined ENCODE (http://www.broadinstitute.org/~anshul/projects/worm/blacklist/ce10-blacklist.bed.gz) and in-house blacklist (https://gist.github.com/przemol/8a712a2e840f95237f4a4f322f65bee1) to generate our final sharp peak calls, described as ‘concave peaks.’ We created a summary peak call super set by creating a union of the five heterochromatin factor concave peak calls. We termed this set ‘Any5’ (n = 33301; Figure 2—source data 1). Each Any5 region was then annotated for overlap with each factor. Venn diagrams were plotted using VennDiagram R package (Chen and Boutros, 2011), and UpSet plots were generated as described in Lex et al. (2014). For determination of factors bound to repeats, we used broad IDR peak calls since repeats usually display a pattern of broad factor binding. Broad IDR peaks were used in Figure 3—figure supplement 2.
We built an exon model based on Ensembl Gene 77 (Nov 2014) database gene annotation lifted over to ce10/WS220. Tag counts for each gene were extracted from BAM alignment files using HTSeq method working in union mode and implemented in R. These values were used to build an expression matrix. Differential gene expression between N2 and mutant backgrounds was tested using DESeq2; mutants were compared to their temperature matched control N2 replicates (Love et al., 2014). Reads per kilobase of exon model per million mapped reads (RPKM) normalized expression values were generated using the median ratio method (Equation 5 in Anders and Huber, 2010). RPKM values, maximum posterior estimates of log2 FC (LFC) and statistical significance estimates for each gene is in Figure 3—source data 3. We used a false discovery rate (FDR) < 0.01 and LFC > 1 to call genes up-regulated, and FDR < 0.01 and LFC < −1 to call genes down-regulated. To avoid small differences in developmental stages from contributing to apparent gene expression differences, we also excluded genes whose wild-type expression oscillates repeatedly during development (Supplemental Table S7 in [Latorre et al., 2015]).
We built a repeat element model based on Dfam 2.0 ([Hubley et al., 2016], downloaded Sept 2015 from http://dfam.org/). The model contained 62331 individual repeats divided into 184 families. Since individual repeats did not had unique identifiers (UID), we named them based on genomic position in ‘chromosome:start-end’ convention, e.g. ‘chrI:10773–11032’. Tag counts for each repeat were extracted from BAM alignment files using HTSeq method working in union mode and implemented in R. These values were used to build expression matrixes. Differential repeat expression between N2 and mutant backgrounds was tested using DESeq2 as described above for genes. A table containing RPKM values, maximum posterior estimates of log2 FC (LFC) and statistical significance estimates for each repeat is available in Figure 3—source data 1. Upregulated repeats were defined as those with a false discovery rate (FDR) < 0.01, and LFC > 0. In addition, repeats that overlapped a gene upregulated in the matched mutant background were filtered out. For purpose of filtering, differentially expressed genes were defined with more permissive cutoffs: FDR < 0.05 and LFC > 0.
To assess expression of individual repeats scored as upregulated above, we counted uniquely mapping reads, defined as having a BWA mapping quality over 10. Elements with >10 unique reads and fold-change >1.5 were considered upregulated, which applied to 61 of 71 elements upregulated in any of the heterochromatin factor mutant strains. The remaining 10 elements had insufficient uniquely mapping reads for assessment.
Telomere enrichment for ChIP-seq factors were determined by counting reads with the telomere sequence ‘GCCTAA’. Reads were extracted from BAM files (including non- aligned reads) and trimmed to 36 bp. Then the number of ‘GCCTAA’ motifs was counted for each read using Biostrings R package. Telomeric reads were defined as those having 5 or 6 ‘GCCTAA’ motifs in 36 bp. To assess the statistical significance of enrichment we used one sided Mann–Whitney U test (two replicates for each factor vs. input background of 129 experiments) and reported the p-values.
The following small RNA datasets from Ashe et al. (2012) were used: prg-1 (GSM708661), WT matching prg-1 (GSM708660), hpl-2 (GSM950181), WT matching hpl-2 (GSM950180), nrde-2 (GSM950179), WT matching nrde-2 (GSM950178). Uniquely matching positions in each dataset were determined and the smallest number (530039, in the prg-1 dataset) subsampled from each. piRNA number was then determined by calculating the number matching the piRNAs annotated in Batista et al. (2008) or Weick and Miska (2014) (n = 27884 piRNAs). piRNA targets were determined as in Lee et al. (2012), requiring a perfect match and no more than one G:U pair in the seed region (nt 2–8), and allowing up to two mismatches and an additional G:U pair outside of the seed region, excluding self hits (n = 391173). piRNA dependent 22Gs were also defined as in Lee et al. (2012), as 22G RNAs that mapped in 100 bp windows centered at piRNA target sites, allowing zero or one mismatch.
The following H3K9me3 ChIP seq datasets were used: nrde-2 (GSM855086), nrde-3 (GSM932875), nrde-4 (GSM932876), WT for nrde-2,–3, −4 (GSM855085), hrde-1 (GSM1399632), and WT for hrde-1 (GSM1399631) from [Gu et al. (2012), Buckley et al. (2012), Ni et al. (2014). Datasets were processed as described in the data processing section above. The average signal in each region of interest was calculated and the H3K9me3 fold change was calculated relative to the matched wild-type dataset. Control repeats (n = 612) have >1.5 fold H3K9me3 levels relative to the genome average, have <1 fold signal for each of the five heterochromatin factors (HPL-2, LIN-13, LIN-61, LET-418 and MET-2) relative to the genome average, and are not upregulated in any of the five mutant strains. A reduction of H3K9me3 at gene and repeat sets of interest was assessed by comparing to all genes or all repeats using a single-sided Mann-Whitney U test.
N2 and hpl-2 adults grown at 25°C were irradiated at 0, 20, and 100 Gy and recovered for one hour at 25°C. One hour post irradiation, gonads were dissected in 8 µL M9 on slides and freeze-cracked. Gonads were fixed four minutes in 100% methanol followed by twenty minutes in 4% formaldehyde in 1 X PBS. After fixation, gonads were washed two times for ten minutes in 1 X PBS + 0.2% Tween-20 (PBST), blocked for one hour at room temperature in 1% milk in PBST, washed two times for ten minutes in PBST, incubated overnight at 4°C in primary antibody diluted in PBST (1:50 rabbit monoclonal α-phospho-CHK-1, Ser345, 133D, Cell Signalling Technologies, catalogue #2348), washed two times for ten minutes in PBST, incubated 2 hr with secondary antibody (Molecular Probes) and DAPI. Gonads were scored for the presence of phospho-CHK-1 staining using a Zeiss 510 Meta scanning-laser confocal microscope. Counts from individual experiments were pooled to give overall totals, and a two-tailed proportions Z test was used to determine whether there was a difference between N2 and hpl-2 worms at a specific condition.
L4 N2 and hpl-2(tm1489) grown at 20°C were irradiated at 0, 50, and 100 Gy, recovered for 24 hr at 20°C, then fixed in MeOH and DAPI stained. Slides were scored for the number of DAPI bodies in diakinesis oocytes. Oocytes with six DAPI bodies, representing the six bivalent chromosomes, were considered normal; oocytes with other numbers of DAPI bodies, representing chromosome fracturing or clumping, were considered fractured. To determine whether the proportion of oocytes with fractured chromosomes was different between N2 and hpl-2(tm1489) worms at a particular condition, a two-tailed proportions Z test was used. Two-tailed P values were calculated using a Z score table.
bcIs39 (Plim7::ced-1::GFP) expressed in gonadal sheath cells, was used to count engulfed germ line corpses (Zhou et al., 2001). Strains containing bcIs39 in wild type and mutant backgrounds were maintained at 20°C. L4s of each genotype were picked and 48 hr later scored for the number of engulfed apoptotic cells in the gonad. A minimum of 25 gonads per experiment were scored in three independent experiments. The number of apoptotic cells in the germ line observed with the ced-1::GFP is higher than the number stained by vital dye or visualized by Nomarski optics because the reporter also marks cells at earlier stages of apoptosis than can be detected by other methods (Lant and Derry, 2014; Lu et al., 2009). In lin-13, hpl-2, and met-2 set-25 strains, full or partial silencing of the GFP transgene reporter occurred in some individuals. These animals were excluded because it was not possible to count cell deaths. Statistical significance was scored using a Mann-Whitney non-parametric test over all the datapoints combined.
Strains were maintained at 20°C and shifted to 25°C at the L4 stage. Adult germlines were imaged 48 hr later by mounting animals on 3% agarose pads in 5 mM Tetramisole, using a Zeiss widefield upright microscope using Nomarksi optics. Oogenesis was deemed ‘abnormal’ if oocytes appeared small and rounded, if they were disorganized, or if their cytoplasm had taken on a pronounced curdled texture. Germlines which had mostly or fully disintegrated, and lacked detectable oocytes, were also quantified.
Fertility interactions among heterochromatin factors were tested as follows: N2, let-418(n3536), and lin-13(n770) were maintained at 20°C. Worms were fed at 20°C from the L4 stage for the following RNAi clones from Kamath et al. (2003): hpl-2 (K01G5.2), met-2 (R05D3.11), and lin-61 (R06C7.7) or from starved L1s for lin-13 (sjj2_C03B8.4). RNAi plates were prepared as in Ahringer, 2006. Progeny of fed L4s or the fed L1were singled out onto fresh RNAi plates as L4s and total broods assessed by transferring the worms to new plates every day until they stopped laying eggs. Two independent experiments were conducted, with 3–8 total broods counted for each strain/RNAi combination. Three double mutant combinations were also constructed and tested: lin-61(tm2649); lin-13(n770), lin-61(tm2649); hpl-2(tm1489), and hpl-2(tm1489); let-418(n3536). Wild-type N2, single mutants, and double mutant strains were maintained at 20°C and total broods counted.
Fertility interactions between nrde-2 and let-418, hpl-2, or lin-61 were tested as follows. Wild-type, single mutants, and double mutants were grown at 15°C from starved L1 until the L3 stage, then transferred to 25°C. Total brood size per worm was determined for 12–24 worms per strain across two independent experiments. Genotypes of strains are given in Supplementary file 2.
Statistical tests for the above genetic interactions were conducted as follows: Under the null hypothesis that the two genes do not interact to affect fertility, the expected brood size of double mutant (or RNAi knockdown in a single mutant background) is the product of those of the single mutants (or that of the single mutant and the RNAi knockdown in a wild type background) divided by the brood size of the wild-type (or of the wild-type strain grown on control (empty vector) RNAi plates). Similar to (Baugh et al., 2005), a t-test was used to test if the observed brood size of double mutants (or RNAi knockdown in a single mutant background) equals the expected brood size under the null hypothesis.
Tests for suppression of sterility of hpl-2(tm1489), lin-13(n770), and let-418(n3536) mutants were conducted mutants as follows. The three strains show temperature sensitive sterility. Strains were maintained at 20°C, a temperature at which they are fertile, and starved L1s prepared by bleaching adults to collect embryos and hatching them in M9 buffer for 24 hr at 20°C. Starved L1s were spotted onto RNAi plates prepared as in Ahringer, 2006. They were then grown under conditions at which the mutant strain is nearly sterile: hpl-2 was incubated at 24°C or 25°C, lin-13 was incubated at 24°C, and let-418 was incubated for 7.5 hr at 20°C, then shifted to 24°C. After three days, the number of progeny produced by these L1s was counted. RNAi plates were prepared as in Ahringer, 2006. The following RNAi clones were from Kamath et al. (2003): cep-1 (F52B5.5), spo-11 (T05E11.4), mirage-A (K02E7.2 + K02E7.3), mirage-B (W03G1.3 + W03G1.4). For each combination of mutant strain and target gene to knockdown, a paired t-test was used to compare the average number of progeny per parent from gene-targeting RNAi plates and matched empty vector plates incubated under the same condition.
Brood sizes of cep-1(lg12501); hpl-2(tm1489), cep-1(lg12501);let-418(n3536) and cep-1(lg12501);lin-13(n770) double mutants were compared to wild-type and single mutants. Adults raised at 15°C were bleached to obtain embryos and left at 20°C to hatch without food to obtain starved L1s. The starved L1s were fed with OP50 bacteria and immediately shifted to 25°C (for hpl-2 tests) or fed at 20°C for 7.5 hr before shifting to 25°C (for let-418 and lin-13 tests). Experiments were repeated at least twice and total brood sizes were determined for 8 to 40 worms per strain. L1s prepared in the same way were used for growth rate tests, counting the number of adults, L4s, or worms younger than L4 (indicated <L4) after approximately 48 hr post feeding. A single sided t-test was used to test whether the brood size of the cep-1 double mutant is larger than that of the single heterochromatin mutant.
mjIs144 [mex-5p::HIS-58::GFP::piRNA(21UR-1)::tbb-2–3’UTR] was used to assess piRNA pathway function (Ashe et al., 2012). Synchronized larvae containing mjIs144 in wild type or mutant backgrounds were maintained at 20°C, and scored for germ line expression 24 hr post-L4 stage. Four experiments were conducted per strain, with a minimum of 25 worms per experiment. GFP was scored using a Zeiss Axioplan two upright widefield microscope, where the level of GFP expression was assessed (none, low, moderate). Moderate expression was scored when GFP was easily detectible in oocytes and pachytene nuclei. Low expression was scored when GFP was just visible in oocyte and pachytene nuclei. In Figure 6, silenced represent gonads with no expression and Expressed - GFP(+) represent moderate or low expression. In the case of met-2, all expression was in the low category.
N2, hpl-2, lin-13, let-418, and prg-1 young adults were fixed and stained by RNA FISH as described (Raj et al., 2008). Stellaris FISH probes targeting MIRAGE1 and sqv-1 (as an internal control) were obtained from Bioresearch Technologies (Novato, CA). CAL Fluor Red610 was used for MIRAGE1 and Quasar 570 was used for sqv-1. From 11–22 individuals per strain were scored.
Datasets generated in this paper are available at GEO accession GSE87524.
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Edith HeardReviewing Editor; Institut Curie, France
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 "A team of heterochromatin factors collaborates with small RNA pathways to combat repetitive elements and germline stress" for consideration by eLife. Your article has been favorably evaluated by Jessica Tyler (Senior Editor) and three reviewers, one of whom, Edith Heard (Reviewer #1), is a member of our Board of Reviewing Editors.
The reviewers have discussed the reviews with one another and the Reviewing Editor has drafted this decision to help you prepare a revised submission.
In this paper, McMurchy, Stempor et al., investigate the relationship between repetitive elements and heterochromatin and the interaction between heterochromatin factors and small RNA pathways in C. elegans. They systematically investigate a series of five heterochromatin factors (HPL-2/HP1, LIN-13, MBT-repeat protein LIN-61, LET-418/Mi-2, and the H3K9me2 histone methyltransferase MET-2/SETDB1) that have fertility phenotypes when mutated, for their binding profiles and for their impact on repeat elements, DNA repair and apoptosis in the germ line. Their results show that these heterochromatin proteins repress the expression (and potentially the noncoding activity – recombination) of repetitive DNA elements in C. elegans germ cells. They also investigate the relationships between these heterochromatin factors and the piRNA and nuclear RNAi pathways. Their study reveals that heterochromatin proteins and small RNA pathways display overlapping as well as unique control of repetitive elements in the germ line.
This work brings several important new insights:
It provides solid genetic and functional links between key factors previously shown to be associated with heterochromatin and known to lead to sterility when mutated.
It demonstrates that derepression of repetitive elements in heterochromatin mutants is one of the reasons these mutants are sterile.
It describes the genomic co-localisation of these five heterochromatin factors, particularly at repetitive elements associated with H3K9 methylation.
It provides new insights into the role that binding of these heterochromatin factors has at repeats, as RNA-seq revealed that although most repeats are derepressed to a small extent, the most affected repetitive elements in heterochromatin mutants were those encoding for transposases – these being the most critical for protection of the germ line from repeat reactivation.
It provides a convincing demonstration that repeat element upregulation is a contributing factor to infertility in heterochromatin mutants by using RNAi knockdown of the repetitive element MIRAGE1 which rescues sterility.
It demonstrates that the piRNA pathway is impeded upon loss of heterochromatin factors by demonstrating the derepression of a piRNA sensor in heterochromatin mutants.
It also shows that the nuclear RNAi pathway is largely independent of the heterochromatin and piRNA pathways, as a very different spectrum of repetitive element derepression was found in nrde-2 mutants compared to the prg-1 piRNA mutant or heterochromatin mutants.
It allows the conclusion, from genetic tests, that these alternate pathways are acting redundantly at some repeats, and uniquely at others.
Overall this is an elegant study, combining genetic and genomic approaches to investigate the role that heterochromatin factors play in repetitive element germ line control and fertility in C. elegans. It provides novel mechanistic insights into the multiple levels at which heterochromatin factors can act, not only in silencing repeats but also participating in DNA repair pathways to maintain genome integrity. The experiments are extremely well conducted, clearly presented and discussed. The interactions between heterochromatin factor pathways and small RNA pathways are still rather tenuous and could be further explored as suggested below.
1) Does upregulation of repetitive elements through loss of heterochromatin disable or overload the piRNA pathway? The authors could address this by small RNA-seq in the different heterochromatin mutant backgrounds, and would expect to see a change in the 21U/22G population if the piRNA pathway is overloaded (i.e. upregulation of a repetitive element leads to a bias in the 22G population in the mutant and a decrease in other 22Gs), or a loss of 21Us if piRNAs are completely eliminated. A simpler experiment might be to see whether any of the RNAi treatments in Figure 4 restore piRNA sensor silencing in the heterochromatin factor mutant backgrounds to link repetitive element expression and/or DNA repair to piRNA pathway function.
2) The authors could use ChIP-seq or immunofluorescence for histone modifications in heterochromatin factor mutant backgrounds in order to demonstrate the loss of heterochromatin marks at repetitive elements. Without such experiments, the connection between heterochromatin proteins and small RNA pathways remains tenuous. If the authors cannot add such experiments they must at least explain and discuss this.
3) In Figure 4: Is the increase in fertility in response to mirage, cep-1, and spo-11 knockdown (KD) a general phenomenon or specific to heterochromatin mutants? The authors could compare the brood size of wt cells with and without KD of the above genes. Measure fold change in wt plus or minus KD and compare to the fold change seen in mutants.
4) Figure 5: how specific is the cep-1-mediated promotion of apoptosis in response to DNA damage? Do cells with no DDR also show an increase in survival if cep-1 is knocked down? The authors could compare the survival of wt cells with and without cep-1 knockdown and compare this to the fold change observed in mutants.
5) The authors should highlight the novelty of their own findings in this manuscript by discussing their contributions in the context of what has been previously published in nuclear RNAi, piRNA and heterochromatin in C. elegans and other organisms e.g. Ashe et al. 2012; Gu et al. 2012; Burton et al. 2011; Buckley et al. 2012; Ni et al. 2014).https://doi.org/10.7554/eLife.21666.039
- Julie Ahringer
- Julie Ahringer
- Alicia N McMurchy
- Eric A Miska
- Alexandra Sapetschnig
- Eric A Miska
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 A Akay for helpful comments on the manuscript. This work was supported by Wellcome Trust Senior Research Fellowships to JA (054523 and 101863). AM was supported by a fellowship from the Canadian Institutes of Health Research, DA by a Darwin Trust scholarship, and AS by an HFSP postdoctoral fellowship. EM was supported by grants from the Wellcome Trust (104640/Z/14/Z) and Cancer Research UK (C13474/A18583). JA and EM also acknowledge support by core funding from the Wellcome Trust (092096) and Cancer Research UK (C6946/A14492).
- Edith Heard, Reviewing Editor, Institut Curie, France
© 2017, McMurchy 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.