MORC1 represses transposable elements in the mouse male germline

Abstract

The Microrchidia (Morc) family of GHKL ATPases are present in a wide variety of prokaryotic and eukaryotic organisms but are of largely unknown function. Genetic screens in Arabidopsis thaliana have identified Morc genes as important repressors of transposons and other DNA methylated and silent genes. MORC1 deficient mice were previously found to display male-specific germ cell loss and infertility. Here we show that MORC1 is responsible for transposon repression in the male germline in a pattern that is similar to that observed for germ cells deficient for the DNA methyltransferase homolog DNMT3L. Morc1 mutants show highly localized defects in the establishment of DNA methylation at specific classes of transposons, and this is associated with failed transposon silencing at these sites. Our results identify MORC1 as an important new regulator of the epigenetic landscape of male germ cells during the period of global de novo methylation.

Introduction

Two Morc genes in Arabidopsis thaliana, AtMorc1 and AtMorc6, were identified in forward genetic screens for novel transcriptional repressors^1,2. AtMORC1 and AtMORC6 are required for silencing of a variety of transposons and are essential for higher-order chromatin compaction. The single MORC gene in C. elegans was also shown to be required for silencing of a repetitive transgene locus¹. The founding member of the Morc gene family is mammalian Morc1. MORC1 is highly expressed in the blastocyst and male germline but is not expressed in most differentiated cells³. Mice deficient for MORC1 are normal except that homozygous mutant males are infertile with small testicles (hence the name microrchidia)^4,5. Male germ cells in the Morc1 mutant do not undergo successful chromosomal pairing during the zygotene stage of meiosis and instead undergo apoptosis, with no germ cells surviving to complete prophase I.

During germ cell development, most DNA methylation is lost between E8.5 and E13.5. Then between E13.5 and birth (approximately E19), the genome undergoes global de novo methylation^6–8. Failure to establish DNA methylation at this time causes transposon upregulation and meiotic failure. Indeed, the meiotic block in the Morc1 mutant is similar to that observed for mice that have defects in DNA methylation and transposon repression, including mice deficient for DNA methyltransferases^9–11 or the pre-meiotic piRNA pathway^12,13. Therefore, we hypothesized that MORC1 might be a critical factor for transposon silencing and DNA methylation in the mouse germline. Here we demonstrate that MORC1 deficient mice undergo transposon derepression starting in late embryogenesis and continuing through the onset of meiosis. We also demonstrate that this phenotype is associated with failed locus-specific de novo methylation targeted specifically towards late methylating transposon sequences.

RESULTS

MORC1 represses transposons in the male germline

In order to further characterize MORC1 we used a previously described FVB/N Morc1 mutant (Morc1^tg) mouse strain in which a tyrosinase gene was integrated into the Morc1 locus⁵. Transgene insertion resulted in loss of exons 2 – 4, eliminating a large region of the GHKL ATPase domain including residues predicted to be critical for catalysis and ATP binding¹⁴ (Fig. 1a). Consistent with previous reports, we found that Morc1^tg/tg mice have a spermatogenesis defect with a complete absence of post-meiotic spermatids and spermatozoa (Supplementary Fig. 1a–c).

Figure 1. MORC1 is a nuclear protein essential for transposon repression.

a, Domain structure of Morc1 gene and disruption in Morc1^tg allele. Deleted residues predicted to be critical for catalytic activity or ATP binding are denoted. b, Detection of MORC1 in E16.5 testes. MORC1 is present as a germ cell specific nuclear protein in the Morc1^+/tg (het) control but is absent from the Morc1^tg/tg (KO). c–d, Aberrant expression of IAP GAG (c) and LINE ORF1p (d) in Morc1^tg/tg as detected by IF P14.5. Note that IAP is overexpressed in most germ cells, whereas LINE is primarily present in the more differentiated cells deeper into the tubule. The scale bars in (b–d) indicate 20µm.

Reverse transcription – polymerase chain reaction (RT-PCR) from wild type (WT), embryonic whole testis indicates that Morc1 mRNA becomes detectable at E14.5 and peaks at E16.5 (Supplementary Fig. 2a), which intriguingly is a period of rapid transposon methylation in the male germline. We generated an antibody against the coiled-coil domain of mouse MORC1 (Supplementary Fig. 2b) and found that MORC1 was localized to the nucleus of male germ cells at E16.5 (Fig. 1b). Conversely, MORC1 protein was undetectable in Morc1^tg/tg mutant germ cells (Fig. 1b). To test for transposon derepression in Morc1^tg/tg germ cells we performed immunostaining for LINE1 ORF1p and intracisternal particle A (IAP) at postnatal day 14.5 (P14.5). We found that both of these transposon classes were ectopically expressed during early postnatal development with particular enrichment of LINE1 ORF1p in the meiotic cells towards the center of the tubule (Fig. 1c, d). LINE1 ORF1p was also derepressed at E16.5 and E18.5, showing that transposon derepression in Morc1^tg/tg arises well before the apparent meiotic defect. (Supplementary Figure 2c).

To identify which genes and specific transposons are targets of Morc1-mediated repression, we performed mRNA-Sequencing (RNA-Seq) of whole testes from Morc1^tg/tg and Morc1^+/tg heterozygous controls at P10.5 and P14.5. Given that germ cells make up only a small percentage of the testis during the embryonic early and post-natal period, we also performed RNA-Seq on rRNA-depleted total RNA from sorted germ cells at E16.5, E18.5, P2.5 and P10.5. To purify germ cells, we crossed the Morc1^tg mutation onto the Oct4-IRES-eGfp reporter strain, which exhibits a distinct eGFP+ population from e9.5 to P2.5 (Supplementary Fig. 3a)^15,16. To isolate germ cells at P10.5, we gated the Side Scatter (SSC) low (SSC^Lo), Epithelial Cell adhesion Molecule (EPCAM) high (EPCAM^Hi) and major histocompatibility complex (MHC) negative (MHCI⁻) population of testicular cells (Supplementary Fig. 3b). A list of sequencing samples and the experiments to which they correspond is included in Supplementary Data 1. Consistent with RT-PCR and published data^5,17, Morc1 mRNA was confirmed to show high expression at E16.5 and lower expression at later time points in the sorted germ cells (Fig. 2a).

Figure 2. Morc1^tg/tg shows transposon upregulation resembling Dnmt3l^−/−.

a, Expression of Morc1 mRNA over development in Morc1^tg/+, as measured by RNA-seq. b–e Overexpression of transposon species over the course of mammalian development, represented as a ratio of expression in the Morc1^tg/tg and the Morc1^tg/+ control. Some LTR transposons show upregulation selectively in late embryogenesis (b) while others are overexpressed postnatally (c–d) and LINE elements are overexpressed both during late embryogenesis and again at the onset of meiosis (e). Overexpression of transposons in MORC1 (f), DNMT3L (g) and MIWI2 (h) deficient whole testis. For a–h. 2–4 replicates per genotype were analyzed, all data is RNA-seq from sorted germ cells. Mean + SE plotted.

The RNA-Seq data showed a broad transposon derepression defect in Morc1^tg/tg starting at E16.5 (Fig. 2c–e, Supplementary Data 2). RT-qPCR analysis of various transposable element classes gave similar results as RNA-Seq data (Supplementary Fig. 4a). In addition, RNA-Seq on sorted Morc1^tg/tg and control germ cells at P10.5 resembled the pattern of transposon derepression observed in whole testes (Supplementary Fig. 4a). Heterozygous Morc1^tg/+ mice showed no marked increase in transposon expression relative to WT Morc1^+/+ mice, confirming their validity as littermate controls (Supplementary Fig. 4b).

Different transposon classes showed different patterns of derepression in Morc1^tg/tg. Some classes (RLTR4, RLTR6, MuRRS, Etn) were upregulated during embryogenesis but silenced even in the knockout at later time points (Fig. 2b). Other transposons (MMERVK10C, GLN, some IAP species) were most highly upregulated at post-natal time points (Fig. 2c–d). LINES were upregulated both in late embryogenesis and again at the onset of meiosis at P14.5 (Fig. 2e), which was confirmed by IF (Fig. 1d, Supplementary Fig. 2c). These fluctuations in transposon upregulation may reflect differences in the inherent transcriptional programs of certain transposon classes, as well as varied effectiveness of other, partially redundant transposon repression pathways at different times. In the aggregate however, these results indicate that MORC1 constitutes a new participant in transposon repression in the mammalian germline, acting on many different elements. Notably, MORC1 silences many transposons classes well after it is downregulated, consistent with it acting through an epigenetic mark such as DNA methylation.

piRNA biogenesis occurs normally in the Morc1 mutant

During this period in germline development (E14.5 to birth), germ cells undergo mitotic arrest and global nuclear reprogramming that most notably involves genome-wide de novo DNA methylation mediated by the DNMT3A/DNMT3L complex^11,18. The pre-meiotic piRNA pathway, involving the nuclear PIWI protein Miwi2, is also active during this period in promoting transposon silencing. In order to evaluate whether MORC1 acts on the same transposon classes as DNMT3L or MIWI2, we performed RNA-Seq on whole testes from Dnmt3l−/−¹⁰ and Miwi2−/−¹² mice and their respective controls at P10.5, and compared this to the Morc1^tg/tg P10.5 whole testis dataset. Morc1^tg/tg and Dnmt3l^−/− exhibited derepression of an overlapping set of transposons, primarily LTR retrotransposons, while the Miwi2^−/− mutant testes had a milder phenotype and showed derepression of specific LINE elements and the IAP-Ey class of retrotransposons, which were not affected in Morc1^tg/tg or Dnmt3l^−/− mutant testes (Fig. 2f–h).

The lack of overlap between Morc1 and Miwi2 predicts that piRNAs would be unperturbed in Morc1^tg/tg mice. To test this we performed small RNA sequencing of testis at E16.5 to examine piRNA production. Our data revealed that the ratio of piRNA/miRNA and the generation of antisense piRNAs were unaltered in Morc1^tg/tg (Table 1), indicating that the piRNA pathway remains largely intact in Morc1^tg/tg testis at E16.5, and that transposon derepression in Morc1^tg/tg is most likely independent of the piRNA pathway. In fact, at P10.5, we observed an increase in the fraction of piRNAs derived from LTR-retrotransposons, especially of the IAP family, in the MORC1 deficient testis (Supplementary Fig. 5a, b, c), similar to that observed in Dnmt3l^−/−19. These LTR transposon-derived piRNAs corresponded to primary sense piRNAs (Supplementary Fig. 5d, e), suggesting that they are likely more abundant simply because the underlying mRNA species are derepressed in Morc1^tg/tg, and some fraction are converted to piRNAs (Supplementary Fig. 5f). Hence our results indicate that MORC1 acts in a transposon-silencing pathway independent of piRNA production.

Table 1. piRNA abundance and characteristics in E16.5 Morc1^tg/+ and Morc1^tg/tg testes.

Ratios of putative piRNA/miRNA, sense piRNA/antisense piRNA and primary piRNA/secondary piRNA populations are indicated for smRNA obtained from pooled E16.5 Morc1^tg/+ and Morc1^tg/tg testes. No substantial defect in piRNA biogenesis is observed in MORC1 deficient testis.

	Morc1 het	Morc1 KO
putative piRNA/miRNA	0.55	0.59
sense/antisense	1.34	1.34
primary/secondary	4.43	3.91

Hypomethylation of transposable elements in Morc1^tg/tg

Because of the resemblance between transposons derepressed in Morc1^tg/tg and Dnmt3l^−/− testes (Figs. 2c and d), we sought to examine whether Morc1 might affect global DNA methylation levels. To address this, we performed whole genome bisulfite sequencing at E16.5, P2.5, and P10.5 on sorted Morc1^tg/tg and control germ cells isolated as above. At E16.5 the germline is undergoing de novo DNA methylation and by P2.5 de novo methylation is largely complete. Between roughly P2.5 and P10.5 germline cells re-enter the cell cycle and either initiate the first wave of spermatogenesis to generate meiotic cells, or localize to the basement membrane and generate the long term self renewing spermatogonial stem cell population^20,21. In contrast to Dnmt3l^−/− mutant germ cells that show a dramatic global reduction in DNA methylation²², we found no change in global levels of methylation at any time point in Morc1^tg/tg sorted germ cells (Fig. 3a). Thus, despite the similar morphological phenotypes and transposon expression defects of Morc1^tg/tg and Dnmt3l^−/− mice, MORC1 does not act by controlling de novo or maintenance methylation at a genome-wide level.

Figure 3. MORC1 regulates DNA methylation in a stage- and locus-specific manner.

a, Total CG and CA methylation levels in Morc1^tg/+ and Morc1^tg/tg sorted germ cells. 3–4 replicates per genotype and timepoint were analyzed, mean and standard error are indicated. b, Number of hypermethylated and hypomethylated DMRs, calculated using pooled BS-seq data at each timepoint. c, Boxplots of DNA methylation levels at E16.5, P2.5 and P10.5 is shown for the set of regions that were computed as hypomethylated at P2.5 in Morc1^tg/tg germ cells. d, Box plots of levels of DNA methylation levels in germ cells at E16.5, P2.5 and P10.5 is shown for the set of regions that were computed as hypomethylated at P10.5 in Morc1^tg/tg. For c–d Each DMR constitutes one point in each box plot. Red lines, median; edges of boxes, 75^th (top) and 25^th (bottom) percentiles; whiskers, minimum and maximum points within 1.5× the interquartile range; red dots, outliers.

In mammals DNA methylation is very dynamic and promoter DNA methylation frequently correlates with gene repression. To determine whether there may be localized defects in DNA methylation in Morc1^tg/tg, and whether these are associated with derepressed transposons identified by RNA-Seq, we calculated statistically significant differentially methylated regions (DMRs) in the Morc1^tg/tg germ cells relative to the Morc1^+/tg control. At E16.5 we found very few DMRs (Fig. 3b). However, at P2.5 we identified 6309 hypomethylated regions (Supplementary Data 3), but only 145 hypermethylated regions (Supplementary Data 4), indicating that Morc1^tg/tg germ cells have locus and stage-specific DNA methylation defects (Fig. 3b). In addition, the overwhelming majority of regions identified as hypomethylated at P2.5 remain hypomethylated at P10.5 (Fig. 3c), and only a few regions lost methylation between P2.5 and P10.5 (Fig. 3d).

The hypomethylated DMRs in Morc1^tg/tg germ cells were highly enriched for LINE and LTR transposons rather than protein-coding genes compared to control regions (see Supplemental Methods), consistent with the transposon expression defects observed in Morc1^tg/tg germ cells (Fig. 4a). Indeed, 93.9% of hypomethylated DMRs contained an LTR or LINE, compared with 40.6% of control DMRs. The hypomethylated DMRs were strongly concentrated in the categories of transposons that showed evidence of deprepression (Figs. 4b–d) during some stage of development prior to meiosis.

Figure 4. Hypomethylated regions in Morc1^tg/tg correspond to upregulated transposon classes.

a,. The overlap of hypomethylated DMRs and control regions (randomly selected regions whose methylation is unaffected by loss of MORC1) with genes and transposon classes is indicated. A DMR or control is counted as overlapping with a feature if there was at least one base-pair overlap. b, Overlap of hypomethylated DMRs with transposon classes upregulated in Morc1^tg/tg. c–d Metaplot of methylation over LINE (c) and LTR (d) retrotransposons. BS-seq data was mapped to annotated RepBase consensus sequences for each transposon class, and methylation is plotted at each CG in the annotated RepBase consensus sequence relative to the consensus sequence. The first fifty bases from each element, which often have low read coverage, are omitted. Because it was usually not possible to determine the orientation of LTR-derived reads relative to LTR-transposons, the average methylation level for the relevant LTR species is shown. e, Global hypomethylation of LTR species corresponding to upregulated transposon classes. Again, BS-seq data was mapped to RepBase consensus sequence for these LTRs.

A partial exception to this trend were IAP elements. Hypomethylated DMRs were strongly enriched IAP elements and corresponding LTRs (Supplementary Fig. 6a), but there was a poor correspondence between the extent to which a subcategory of IAPs was upregulated and the frequency of overlap with DMRs (Fig. 2d, Supplementary Fig. 6b). This is likely because certain highly similar repetitive elements such as LTR1 give very few uniquely mapping reads and are therefore missing from the dataset. To overcome this, we also mapped the BS-seq data to RepBase consensus sequences for relevant transposons. We confirmed hypomethylation of the upregulated IAPLTR1 class (Supplementary Fig. 6c). Mapping to repeat consensus sequences also confirmed hypomethylation of LINE and LTR classes, which frequently overlap with DMRs (Fig. 4c–e).

Only 20 protein-coding genes contained an annotated transcription start site (TSS) within 1kb of a hypomethylated DMR (Supplementary Data 5), and only 3 contained a TSS within a DMR. Interestingly, all three of these genes (Nebulin, Tmc2, Cdkl4) contain an RLTR10A transposable element immediately upstream of the TSS and all three genes showed a statistically significant increase in expression (Supplementary Fig. 7, Supplementary Data 5). Thus, at a very few loci, MORC1 regulates genic expression, probably as a byproduct of its transposon repression activity in the local neighborhood.

Considering MORC1’s role as local modulator of DNA methylation, we examined changes in methylation in the three well-characterized paternally methylated imprinted loci²³. Methylation occurred normally at two of the three loci (H19 and Dlk1-Gtl2) but the imprinting control region of Rasgrf1 showed increased transcription and hypomethylation in the Morc1 mutant (Supplementary Fig. 8). Interestingly, this is a transposon rich area which has previously been demonstrated as a target of the piRNA pathway²⁴ (see Discussion below).

Of the very few hypermethylated loci observed in the Morc1 mutant, most were not conserved across time points, and are probably a consequence of biological or statistical noise. However, 15 hypermethylated DMRs were reproducible between P2.5 and P10.5. Nine of these fifteen were embedded in two transcripts upregulated in Morc1^tg/tg: six DMRs contained within the body of the Cdkl4 gene described above and three DMRs in an unannotated transcript probably originating in a hypomethylated IAPLTR1 element (Supplementary Fig. 9). This is likely an example of transcriptional run-through from a nearby promoter causing methylation of a locus, a phenomenon that has been described for some imprinted loci²⁵.

DMRs are sites of transposon transcriptional initiation

The highly localized affect of MORC1 on the germline epigenome suggests that MORC1 may function at the transcriptional start sites of transposons to facilitate their silencing and methylation. In support of this, we discovered that hypomethylation in Morc1^tg/tg mutant germline cells was concentrated at the 5’ ends of LINE elements coincident with the location of transcriptional initiation (Fig. 4c)²⁶. Furthermore, LTR transposons, which are typically flanked by LTRs that serve promoter and enhancer functions²⁷, showed hypomethylation on both ends in Morc1^tg/tg (Fig. 4d), and the LTRs themselves are heavily hypomethylated (Fig. 4d,e).

We also noted that hypomethylated DMRs in Morc1^tg/tg germ cells were late targets for de novo methylation during the course of control epigenetic reprogramming since in control Morc1^tg/+ cells these genomic regions were also hypomethylated relative to the genome average at E16.5 (Fig. 3c,d; Supplementary Fig. 10). This suggests that these loci are somewhat resistant to de novo methylation. Consistent with this possibility we also discovered that these Morc1 affected genomic regions have increased H3K4me3 relative to control regions of the genome in wild type cells E13.5 (Supplementary Fig. 11a)²⁸. In order to determine whether these loci are enriched in H3K4me3 during the dynamic de novo methylation of the germline genome we performed ChIP for H3K4me3 at E16.5 and confirmed that these regions still exhibited higher H3K4me3 (Fig. 5a). In contrast, other chromatin marks such as H2B10ac, K3K27ac, H3K27me3 showed no correlation with Morc1^tg/tg DMRs (Supplementary Fig. 11b). It is well established that H3K4 methylation antagonizes de novo DNA methylation by blocking DNMT3A/3L binding to histone H3²⁹. Thus, the presence of H3K4me3 could potentially explain why they methylate with slow kinetics and require an additional factor (MORC1) for eventual silencing and methylation. It is also well established that H3K4me3 is a mark of transcriptional start sites, consistent with the idea that many DMRs are transcription start sites for transposons that are active in the embryonic germline.

Figure 5. Hypomethylated regions in Morc1^tg/tg correspond to TSS of transposons active in late embryogenesis.

a, H3K4me3 abundance is calculated within regions identified as hypomethylated DMRs (Hypo DMR) in P2.5 Morc1^tg/tg germ cells and over a control set of regions

b, Average distributions of uniquely mapping E16.5 RNA-Seq reads (left) and P10.5 RNA-seq reads (right) from individual replicates are plotted over regions identified as hypomethylated at P2.5. c, Pooled E16.5 ATAC-seq reads are plotted relative to methylation distribution at two loci with hypomethylated DMRs. Each CG is represented as by a bar, with the height of the bar indicating the frequency with which the CG is methylated. A dot at a position indicates no methylation. At least one read must map to the CG for a bar to appear. d, ATAC-seq reads from individual replicates at E16.5 (left) and P10.5 (right) are plotted relative to DMRs. e, ATAC-seq read abundance at DMRs and adjacent regions is represented as a boxplot, with each DMR constituting one point in the boxplot.

At E16.5 we found that RNA transcripts were significantly elevated at Morc1^tg/tg hypomethylated DMRs relative to the surrounding areas, even in control Morc1^tg/+ germ cells (Fig. 5b). However, by P10.5, this RNA expression was severely repressed in control Morc1^tg/+ germ cells with modest but increased expression in Morc1^tg/tg (Fig. 5b). This data is consistent with a model in which the hypomethylated DMRs correspond to transcription start sites that are normally methylated and suppressed during development.

To further confirm that these DMRs correspond to transcriptional start sites, we employed ATAC-seq, which can be used to identify areas of open chromatin that are a signature of promoter and enhancer sites³⁰. We confirmed that ATAC-seq can be accurately adopted for small sample sizes, that reads cluster near transcriptional start sites in E16.5 germ cells, and that ATAC-seq read density at the TSS correlates with gene expression (Supplementary Fig. 12). We found that ATAC-seq peaks overlapped tightly with DMRs, (Fig. 5c,d), and most DMRs showed ATAC-seq reads substantially elevated over background (Fig. 5e). In contrast, reads from the naked DNA control were not enriched over DMRs (Fig. 5d). At P10.5, a more limited subset of DMRs exhibited elevated ATAC-seq reads (Fig. 5e), consistent with the observation that transcription is retained only at some DMRs in post natal germ cells (Supplementary Fig. 13a,b). Other sites lose ATAC-peaks and transcription (Supplementary Fig. 13c), either because relevant transcription factors are absent or because other mechanisms of transposon silencing are effective. Importantly, at E16.5 where we observe expression from DMR regions in both Morc1^tg/+ and Morc1^tg/tg cells, we also observed a high ATAC-seq signal in both Morc1^tg/+ and Morc1^tg/tg cells (Fig. 5d). In contrast, at P10.5 where DMRs are silenced in heterozygotes, but remain expressed in Morc1^tg/tg, we only observed high ATAC-seq signal in the Morc1^tg/tg cells (Fig. 5d). These results support the view that DMRs in Morc1^tg/tg cells correspond to promoters of transposons that fail to silence properly, leading to an inappropriately open chromatin state, and ectopic transposon expression, which is retained at P10.5, even after MORC1 expression has ceased.

DISCUSSION

The results of this study identify MORC1 as a critical regulator of transposon repression in the male germline. MORC1 does not act as a global regulator of DNA methylation. Instead, MORC1 functions to facilitate DNA methylation of a variety of transposons in the germline with very little affect on the expression or methylation of protein coding genes. The observation that Morc homologs are required for gene silencing in Arabidopsis, C. elegans, and now mammals suggests that the Morc family of proteins constitute conserved epigenetic regulators that likely function in a wide variety of eukaryotic organisms and developmental contexts.

The Morc1^tg/tg, phenotype of transposon derepression and a block in meiosis prophase I superficially resembles the phenotype observed in mice deficient for proteins involved in the pre-pachytene piRNA pathway, including Mili^31,32, Miwi2¹², MitoPLD³³, Mov10L1^34,35, Mael^36,37, Tdrkh³⁸, Tdrd9¹³, and MVH^39,40. What distinguishes Morc1^tg/tg from these characterized pre-pachytene piRNA mutants however is the apparently normal piRNA biogenesis in Morc1^tg/tg (Table 1). We do note similarities in the pattern of hypomethylation in Morc1^tg/tg and Mili^−/− mutant germ cells, including the Rasgrf1 imprinting control region²⁴, as well as many of the same transposon families⁴¹. The dissimilarity in transposon repression observed in Miwi2^−/− and Morc1^tg/tg germ cells (Figure 2 f,h) suggests that MORC1’s role in the nucleus is independent from the nuclear piRNA pathway mediated by MIWI2. It is possible that MORC1 participates downstream of the nuclear piRNA pathway during embryogenesis, and has a separate, piRNA-independent silencing role during the postnatal stages. This could cause Morc1^tg/tg to have a broader transposon derepression phenotype than Miwi2^−/−. Alternatively, there may exist a MILI dependent, MIWI2-independent mechanism for promoting methylation of target loci.

TEX19.1 has also been implicated in transposon repression in the male germline and has no known link to the piRNA pathway⁴². However, TEX19.1 is cytoplasmic^42,43, shows dysregulation only of MMERVK10C elements^42,44, and Tex19.1^−/− has an incomplete infertility defect^42,43. Thus the Morc1^tg/tg and Tex19.1^−/− defects are fairly dissimilar and there is no evidence that they participate in the same pathway.

Although we have revealed a critical role for MORC1 in transposon silencing, the actual mechanism by which MORC1 promotes DNA methylation in the male germline is unknown. Our study suggests at least three potential routes by which MORC1 represses transposons and facilitates DNA methylation. One possibility is that MORC1 directly silences transcription, perhaps utilizing its ATPase activity to compact chromatin, thereby reducing H3K4 methylation levels at target sites. This silencing would allow for normal de novo methylation by DNMT3L. A second possibility is that MORC1 could recruit an H3K4 demethylase, which would similarly promote DNA methylation. Either mechanism agrees with our observation that MORC1 hypomethylated DMRs originate from loci with increased H3K4me3 at E13.5. A third non-mutually exclusive possibility is that MORC1 directly recruits the DNA methylation machinery to target loci, mediating methylation and silencing.

In conclusion a robust genome defense system in the male germline is critical to safeguard genome integrity. We have identified a new participant that acts by facilitating DNA methylation of specific repetitive elements classes.

METHODS

Mice

FVB/N-Morc^tg/+(Tyr)1Az/J mice (Morc1^tg) were recovered from cryopreservation at the Jackson laboratory and maintained by intercrossing brothers and sisters in the FVB/N background. Male Morc1^tg/tg mice were viable healthy but infertile, whereas female Morc1^tg/tg mice were viable healthy and fertile. For PCR genotyping the wild type allele was detected as a 347bp band with the following primers; forward: 5’-ATGCAACTTGAGGGGAAACA-3’ and reverse: 5’-GCAGGAGTTATGCGATGTCA-3’, and the mutant allele was detected as a 244bp band with the following primers; forward: 5’-AGTTAGCCGTTATTAGTGGAGAGG-3’ and reverse: 5’-AGAAAGCCTGCCTCAAAACA-3’. PCR conditions involved ten cycles of 94°C 65°C and 68°C followed by 28 cycles of 94°C, 50°C and 72°C. For sorting germ cells from E16-5-P2.5, Morc1^tg/tg females were crossed into the Oct4-IRES-Gfp mixed background. For embryonic staging timed-pregnancies were established and the day a vaginal plug was identified was called embryonic day 0.5 (E0.5). For postnatal time points the day a litter was first observed was referred to a postnatal day 0.5 (P0.5).

All animal experiments were approved by The UCLA Institutional Animal Care and Use Committee, also known as the Chancellor's Animal Research Committee (ARC)

Antibodies

Murine Morc1 coiled-coil domain (amino acids 788–950), expressed in and purified from bacteria, was provided by Jiamu Du and Dinshaw Patel (Sloan Kettering). Anti-Morc1 antibody was raised in rabbit in collaboration with Rockland Immunochemicals.

Anti-LINE Orf1p antibody was provided by Alex Bortvin (Carnegie Institution for Science), anti-IAP Gaga antibody was provided by Bryan Cullen (Duke).

Immunofluorescence

Whole testes were fixed with 4% paraformaldehyde, immobilized in paraffin and sectioned. After removal of paraffin, sections were stained at the following antibody concentrations: anti-LINE Orf1p (1:300), anti-IAP Gag (1:300), anti-MORC1 (1:100), anti-VASA (1:100, R&D Systems AF2030), stained with fluorescent secondary antibody and mounted with DAPI. Slides were imaged by Confocal microscopy.

Embryonic germ cell purification

Collection of embryonic testes were performed following institutional approval for appropriate care and use of laboratory animals. Pregnant females were euthanized using CO₂ and the embryos removed from the womb and stored on a 10cm dish filled with chilled 1×PBS. Testicles were removed from the embryos, placed in an individual 15ml falcon tube with 3mls of 0.25 % Trypsin with 3µl of DNAse I 1Unit/1µL (Life Technologies). Testes were incubated for 15mins at 37C. After incubation the cells were agitated into suspension gently by pipetting. The trypsin was then quenched using 5mL DMEM/10% FBS (Life Technologies). The cells were centrifuged at 278g for 5 minutes and resuspended in 500uL FACS buffer (1×PBS 1% BSA). 7-AAD was added at a 1:50 dilution (BD Biosciences) and the cells strained through BD FACS tubes (Corning) before analysis. GFP positive cells were sorted into Buffer RLT or ATL for RNA or DNA extraction respectively.

Postnatal germ cell purification

Pups were euthanized using isoflourane. The testes were removed using tweezers, placed in a 1.5ml centrifuge tube and chilled on ice. When all testes had been removed, each pair was placed in 1 ml of type IV collagenase (Invitrogen) in a ultra low-attachment 6-well plate (Corning). All extraneous tissue and the tunica were removed and the seminiferous tubules were teased apart. The samples were then incubated 37°C 15 minutes and centrifuged for 5 minutes at 278g. Testes were then resuspended in 500µl of 0.25% Trypsin (Life Technologies) and incubated for 5 minutes at 37°C. After the incubation period the testes were agitated gently into suspension by pipetting. 500ul DMEM/10% FBS was added and the samples were centrifuged for 5 minutes at 200g.

For the P2.5 timepoints GFP positive cells were sorted as with embryonic time points. To sort germ cells at P10.5, the cells were washed with 1mL FACS buffer and then resuspended in 500µL FACS buffer. Then cells were then incubated with 1:160 EPCAM PE (Biolegend 118205) and 1:250µL H2-K^q 647 (Biolegend 115106) on ice for 20 minutes in the dark, then centrifuged 5 minutes at 200g and resuspended in 500µL FACS buffer. DAPI was added (1:1000, Life Tech) and the cells were strained through BD FACS tubes (Corning) before analysis. SSC^lo EpCAM^hi H2-K^q− cells were sorted into Buffer RLT or ATL for RNA or DNA extraction respectively.

Quantitative RT-qPCR of Morc1

For embryonic samples, gonads were pooled from ~5–7 mice per timepoint. RNA was extracted by the TRIzol method and DNase-treated (Qiagen) prior to cDNA conversion (Superscript III, Life Technologies). Quantitative amplification of cDNA was performed in triplicate using SYBR Green quantitation (PCR primers listed below) on a 7900 HT Fast Real Time PCR System (Applied Biosystems).

Rrm2	F : CCGAGCTGGAAAGTAAAGCG
	R : ATGGGAAAGACAACGAAGCG
Morc Exon 7	F : GACCCGCAGAAGTTCTTCA
	R : TGCTGCATCAATTCAGCTTC

RNA preparation

RNA for was extracted from whole testes or cells using the RNeasy Micro Kit (Qiagen 74004). The material was quantified using a Nanodrop ND-1000 (Nanodrop) for RNA from whole testis or the Qubit RNA High Sensitivity Assay (Life Technologies) for RNA from sorted germ cells. RNA quality for material from whole testis was assessed by gel electrophoresis and visualization of the 28S and 18S rRNA bands.

DNA preparation

DNA for bisulfite sequencing was extracted using the QiaAMP DNA Micro kit (Qiagen) and quantified using the Qubit dsDNA High Sensitivity Kit (Life Technologies).

Quantitative reverse transcription-PCR

Quantitative reverse transcription-PCR (qRT-PCR) for retrotransposons was conducted using published primer sets⁴⁵. 1µg total RNA was treated with DNAse I Amplification Grade (Life Technologies) and converted to cDNA using SuperScript II Reverse transcriptase and random hexamers as primer (Life Technologies). The samples were digested with RNAse H in accordance with manufacturer protocol. RT-PCR was then performed using iQ SYBR Green Mastermix (BioRad) with 750nM concentration of each primer. The PCR program was 10 minutes 95°C; 50 cycles of 30s 95°C, 30s 55°C 30s, 72°C 30s; with detection of PCR product after each elongation step and determination of melting temperature after the completion of PCR. The reaction was performed using an Agilent Technologies Mx3005p qPCR System (Stratagene). Upregulation of transposon transcript in the mutant is estimated using difference of squares with GAPDH as a control.

RNA-seq library preparation

RNA from whole testes was processed for sequencing using a TruSeq RNA Sample Preparation Kit v2 (Illumina) with 250ng - 2µg total RNA as starting material. Mutant and controls were always matched for starting RNA content. RNA from sorted germ cell was processed using the Ovation Human FFPE RNA-Seq Multiple kit (Nugen) using custom primers for depletion of murine rRNA provided by the manufacturer, using 10ng of total RNA. Each library was prepared using RNA from one individual mouse.

Small-RNA isolation and library preparation

Total RNA was isolated from embryonic testes using Ribozol. Thirty µg total RNA was loaded on 12% urea-polyacrylamide (PAA) gel. The 19–30 nt fraction was excised and snap-frozen in liquid nitrogen in 400 µl 0.4M NaCl. RNA was eluted from the gel overnight at 16°C while shaken at 1,000 rpm and then precipitated with 3 vol absolute ethanol. Pre-adenylated 3’ linker (/5`Phos/TGGAATTCTCGGGTGCCAAGGAACTC/3`ddC/; 5’DNA adenylation kit, NEB) was ligated to RNA over night at 4C using Truncated RNA Ligase 2 (NEB). Ligation reactions were loaded onto 10% urea-PAGE, the 45–56 nt fraction was excised and nucleic acids extracted as above. 5’ linker (rGrUrUrCrArGrArGrUrUrCrUrArCrArGrUrCrCrGrArCrGrArUrC) was ligated to the samples using RNA Ligase 1 (NEB) over night at 4C. Ligation reactions were loaded on 10% Urea-PAA gel, 72–83 nt fraction was excised and nucleic acids as above. Extracted samples were reverse-transcribed (primer sequence: GGAGTTCCTTGGCACCCGAGA) and library amplified by PCR using standard Illumina primers. Final libraries were excised from the agarose gel and sequenced.

Bisulfite library preparation

Libraries were prepared using the Ovation Ultralow Methyl-Seq Library System (Nugen). 5ng – 25ng DNA was used as starting material. Matched mutant and control samples always contained identical quantities of DNA. Unmethylated Lambda phage DNA (NEB) was spiked in at 0.5% input DNA quantity to determine conversion efficiency, which was consistently >98%. Each library was prepared using DNA from one individual mouse.

ChIP-seq

The ChIP-seq protocol was adapted from published sources²⁸. FACS sorted cells from an individual mouse were diluted to 292µL with room temperature 1×PBS. 8.11µL 37% Formaldehyde (Sigma) was added and the sample was incubated 10 minutes at room temperature with rocking. 48.8µL of 1M glycine was then added to yield a final concentration of 0.14M and the samples were quenched 30 minutes with rocking. Cells were then spun 425g for 10 minutes at RT. The cell pellet was flash frozen.

After thawing, the cells were resuspended in 200µL Lysis buffer (50mM Tris-Cl pH 8.0, 20mM EDTA pH 8.0, 1% SDS, 1× Complete Protease Inhibitor(Roche)) and incubated on ice ten minutes. Samples were then subjected to a nine minutes disruption using a Bioruptor on “High” setting, with 30s/30s off disruption (so 4.5 minutes of disruption total). Samples were spun 14000g 10 minutes to remove insoluble material. The soluble sample was diluted to 500µL with dilution buffer (16.7mM Tris pH 8, 0.01% SDS, 1.1% TritonX-100, 1.2mM EDTA, 167mM NaCl) and 10% of material was saved as input. Sample was precleared with 30µL Protein A Dynabeads (Life Technologies) and preincubated 1hr. The cleared material was incubated with 1µL L anti-H3K4me3 antibody (Millipore 04-745) overnight.

The samples were incubated with 30µL Protein A Dynabeads and the precipitated material was recovered with a magnet. The beads were washed 2×4 minutes with Buffer A (50mM HEPES pH 7.9, 1% Triton X-100, 0.1% Deoxycholate, 1mM EDTA, 140mM NaCl), 2×4 minutes with Buffer B (50mM HEPES pH 7.9 0.1% SDS 1% Triton X-100 0.1% Deoxycholate, 1mM EDTA, 500mM NaCl) and 2×4 minutes with 10mM Tris/1mM EDTA. Bound material was eluted with 100µL Elution buffer (50mM Tris pH 8.0, 1mM EDTA, 1% SDS) at 65C for ten minutes and then eluted a second time with 150µL elution buffer.

The input samples were thawed and diluted with 200µL buffer. Crosslinking of ChIP and input samples was reversed by incubating 16 hours at 65C. Samples were cooled and treated with 1.5µl of 10mg/mL RNaseA (PureLink RNAse A, Invitrogen #12091-021) for thirty minutes at 37C. 100µg of Proteinase K was then added and the samples treated for 2hr at 56C. The samples were then purified using a Qiagen Minelute kit.

Samples were amplified by a SeqPlex DNA Amplification kit (Sigma) and then converted to libraries using an Ovation Rapid Library kit.

ATAC-seq library construction

Libraries were generated using a method adapted from published protocol³⁰. Briefly, FACS collected cells from individual mice were spun 500g × 5 minutes at 4°C. Cells were resuspended in 50µL lysis buffer (10mM Tris pH 7.4, 10mM NaCl, 3mM MgCl₂, 0.1% NP40, 1× Complete Protease Inhibitor(Roche)) and spun 10 minutes 500g 4°C to collect nuclei. The nuclei were resuspended in 50µL Transposase reaction (25µL 2×Tagmentation buffer, 22.5µL water, 2.5µL Tn5 Transposase enzyme) and reacted for 30 minutes at 37°C on a PCR machine. The material was purified using a Qiagen MinElute protocol, eluting with 14µL EB.

To amplify ATAC-seq libraries from the treated material, we amplified using the Ad1 primer below and a different Ad2 primer for each sample which functions as a barcode

• Ad1: AATGATACGGCGACCACCGAGATCTACACTCGTCGGCAGCGTCAGATGTG

• Ad2.1_TAAGGCGA: CAAGCAGAAGACGGCATACGAGATTCGCCTTAGTCTCGTGGGCTCGGAGATGT

• Ad2.2_CGTACTAG: CAAGCAGAAGACGGCATACGAGATCTAGTACGGTCTCGTGGGCTCGGAGATGT

• Ad2.3_AGGCAGAA: CAAGCAGAAGACGGCATACGAGATTTCTGCCTGTCTCGTGGGCTCGGAGATGT

• Ad2.4_TCCTGAGC: CAAGCAGAAGACGGCATACGAGATGCTCAGGAGTCTCGTGGGCTCGGAGATGT

• Ad2.5_GGACTCCT: CAAGCAGAAGACGGCATACGAGATAGGAGTCCGTCTCGTGGGCTCGGAGATGT

• Ad2.6_TAGGCATG: CAAGCAGAAGACGGCATACGAGATCATGCCTAGTCTCGTGGGCTCGGAGATGT

• Ad2.7_CTCTCTAC: CAAGCAGAAGACGGCATACGAGATGTAGAGAGGTCTCGTGGGCTCGGAGATGT

• Ad2.8_CAGAGAGG: CAAGCAGAAGACGGCATACGAGATCCTCTCTGGTCTCGTGGGCTCGGAGATGT

• Ad2.9_GCTACGCT: CAAGCAGAAGACGGCATACGAGATAGCGTAGCGTCTCGTGGGCTCGGAGATGT

• Ad2.10_CGAGGCTG: CAAGCAGAAGACGGCATACGAGATCAGCCTCGGTCTCGTGGGCTCGGAGATGT

The eluted material was amplified in 50µL volume using 1.25µM primer concentration and a 1× concentration NEBNext High-Fidelity Master-Mix (NEB) (Program: 72°C 5:00, 98°C 30s, 5× (98°C 10s, 63°C 30s, 72°C 1 minute), 4°C hold). After these 5 cycles of amplification, the tube was kept on ice.

A 5 µL aliquot was then removed and used to perform a 15 µL side reaction with identical concentrations of primer and enzyme, except that 0.6× SYBR Green (Invitrogen S-7563) is included to monitor amplification. This side reaction was amplified on a Stratagene Mx3005p qPCR (Agilent) system with the following amplification conditions (98°C 30s, 20× (98°C 10s, 63°C 30s, 72°C 1:100)). The number of additional cycles ‘N’ required to reach ¼ maximum fluorescence was observed. The purpose of this side reaction was to minimize the number of PCR cycles required used to generate the libraries, since length and GC bias increases with more amplification The remaining 45µL of the reaction was then further amplified (98°C 30s, N × (98°C 10s, 63°C 30s, 72°C 1:00), 4°C) and the libraries were puried by a Qiagen MinElute kit eluting with 20 µL volume. Libraries were visualized by running on a 5% TBE gel and imaged by incubating for twenty minutes in 1×SYBR Green/1×TBE. Libraries quantified using the KAPA Library Quantification Kit (Kapa Biosystems).

RNA-seq analysis

For all analyses, reads were trimmed to 50bp and those mapping to ribosomal RNA (GenBank identifiers: 18S NR_003278.3; 28S NR_003279.1; 5S D14832.1; 5.8S K01367.1) by up to three mismatches were discarded.

Analysis on repeat families

Reads were then mapped to the mm 9 genome allowing no mismatches and keeping reads that map up to 10,000 sites in the genome using Bowtie⁴⁶. Each mapping read was assigned a score of 1/n, where n is the number of sites in the genome the read mapped to. Repeats were obtained from Repeat Masker. Expression values for each repeat family was calculated by adding the scores contained within the repeat body, dividing by the total million reads mapped and average length (kb) of repeats within the family.

Analysis on individual genes and repeats

Reads were then mapped to known mm 9 gene and repeat annotations by allowing up to two mismatches and only retaining reads that mapped to one location. When reads did not map to the annotated genes and repeats, the reads were mapped to the mm9 genome. Number of reads mapping to genes and repeats were determined by using HTSeq (doi: 10.1101/002824) using default parameters. Expression values were calculated as reads per kilobase of exons per million mapping reads (RPKM). Differential gene and repeat expression was determined by using DESeq⁴⁷ using default parameters.

Whole genome bisulfite sequencing

Reads were split into 50bp reads prior to mapping. Reads were mapped to the mm 9 genome as well as the lambda genome using BS seeker2⁴⁸ using default parameters. Methylation levels were determined by #C/(#C+#T). For identifying differentially methylated regions (DMRs), the genome was tiled into 500bp bins, and CG methylation levels in KO and control were compared within each bin. Bins that had a methylation level difference of 50% as well as a FDR<0.05 calculated by Fishers Exact Test corrected by the Benjamini-Hochberg procedure were selected. Finally, DMRs containing at least four cytosines in CG contexts each covered by at least four reads were retained. Control regions were defined completely randomly except that control regions have: 1. Exact same coverage of cytosines in CG contexts as the Morc1^+/tg data within DMRs. 2. Wild type CG methylation levels are similar as the Morc1^+/tg data within DMRs (<5%). 3. Same number of regions per chromosome as DMRs. We defined genes as associated with DMRs when the TSS of an Ensembl transcript model was within 1kb of a DMR.

In order to align to Repeat consensus sequences, the RepBase consensus sequences for thirty repetitive elements (B1_SINE, ERVB7 1-I MM (EtnERV2/MusD), IAP-d, IAPEY3_I, IAPEY_I, IAPEY_LTR, IAPEY3_LTR, IAPEZI, IAPLTR1_Mm, IAPLTR2_Mm, IAPLTR3, IAPLTR3_I, IAPLTR4, IAPLTR4-I, L1MdA_I, L1MdF_I, L1MdGf_I, L1MdTf_I, First 234 bases of GSAT_MM (Major_satellite), MMERGLN_I, MMERGLN_LTR, MERVL, MERVL_LTR, First 120 bases of SATMIN (Minor_satellite), MMERVK10C, RLTR10C, RLTR27_MM, RLTR6_MM, RLTR6I_MM, RLTRETN_MM, RSINE1 were combined into a microgenome. Then, whole genome bisulfite sequencing reads were mapped to the microgenome using BSMAP⁴⁹ allow up to 1 multiple hits [−w 1], map to two forward possible strands [−n 0] and allow 2 mismatches [−v 2]. Methylation levels were determined by #C/(#C+#T). The methylation levels at each CG site was calculated.

Small RNA sequencing

Sequence adaptors were removed using a custom designed dynamic programming algorithm that recognizes both exact and inexact matches and the trimmed reads were aligned to the mm9 genome following a custom suffix array based procedure⁵⁰. Reads with lengths greater than 24 nt were considered for piRNA analysis. Based on alignment coordinates, the reads were annotated as derived from exons, introns, transposons and other repeats according to the genome annotation obtained via UCSC Genome Bioinformatics⁵¹. Reads that had multiple valid alignments were annotated based on ten alignments selected at random, and the majority annotation was assigned as the final annotation. In case of ties, annotation was picked based on a fixed hierarchy principle⁵⁰. Sense or antisense annotation was assigned to piRNA reads with the respect to the strandedness of an underlying genomic feature. If a piRNA read contained U in position 1, such piRNA was considered as primary, while presence of A in position 10 defined secondary piRNAs.

ChIP-seq analysis

Previously published ChIP-seq data²⁸ was obtained from GSE38165 in Gene Expression Omnibus. Reads were mapped to the mm9 genome using Bowtie by allowing up to two mismatches, and only retaining reads that mapped to one location in the genome. Reads mapping to the same location were collapsed into one read. For all analyses, the data were normalized to total number of mapping reads in the library

ATAC-seq analysis

Data were collected using 50bp paired end sequencing on a HiSeq. In keeping with established methodologies³⁰, reads were aligned to mm9 using Bowtie⁵² with the parameters −X2000 and −m1. The −X2000 parameter allows the fragments less than 2kb to align and only unique aligning reads were collected (−m1). Duplicated reads were removed with samtools (rmdup function)⁵³. Previous results show that for Tn5 transposase, the transposon binds as a dimer and insert two adaptors separated by 9bp⁵⁴. Thus, all reads aligned to the + strands were offset by +4bp, and all reads aligned to the – strands were offset by −5bp.