MORC Family ATPases Required for Heterochromatin Condensation and Gene Silencing

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Science  15 Jun 2012:
Vol. 336, Issue 6087, pp. 1448-1451
DOI: 10.1126/science.1221472


Transposable elements (TEs) and DNA repeats are commonly targeted by DNA and histone methylation to achieve epigenetic gene silencing. We isolated mutations in two Arabidopsis genes, AtMORC1 and AtMORC6, which cause derepression of DNA-methylated genes and TEs but no losses of DNA or histone methylation. AtMORC1 and AtMORC6 are members of the conserved Microrchidia (MORC) adenosine triphosphatase (ATPase) family, which are predicted to catalyze alterations in chromosome superstructure. The atmorc1 and atmorc6 mutants show decondensation of pericentromeric heterochromatin, increased interaction of pericentromeric regions with the rest of the genome, and transcriptional defects that are largely restricted to loci residing in pericentromeric regions. Knockdown of the single MORC homolog in Caenorhabditis elegans also impairs transgene silencing. We propose that the MORC ATPases are conserved regulators of gene silencing in eukaryotes.

Gene silencing in the Arabidopsis genome is highly correlated with DNA methylation, which is found in three different cytosine contexts. Methylation of symmetric CG and CHG sites (in which H is A, T, or C) are mediated by DNA METHYLTRANSFERASE1 (MET1) and CHROMOMETHYLASE3 (CMT3), respectively, whereas CHH methylation is mainly catalyzed by DOMAINS REARRANGED METHYLTRANSFERASE2 (DRM2) (1). Silent loci are also enriched in the repressive histone H3 lysine 9 dimethylation mark (H3K9me2) (2, 3).

Suppressor of drm2 cmt3 (SDC) is a gene whose repression in most tissues depends on the redundant activities of DRM2 and CMT3 (4, 5). Hence, a loss of SDC silencing is observed in the drm2 cmt3 double mutant but not in drm2 or cmt3 single mutants. The SDC promoter carries seven tandem repeats, which recruit the DNA methylation machinery and cause transcriptional gene silencing. We engineered a green fluorescent protein (GFP)–based sensor construct controlled by the SDC promoter (fig. S1A). The SDC::GFP transgene behaves similarly to endogenous SDC, and GFP fluorescence is not detectable in wild-type, drm2, or cmt3 plants but is highly expressed in drm2 cmt3 double mutant (Fig. 1A).

Fig. 1

Mutations of two MORC homologs induce SDC::GFP and TE overexpression. (A) wt, drm2 mutant, and cmt3 mutant plants carrying SDC::GFP showed no GFP fluorescence under ultraviolet (UV) light (insets show each plant under white light), and drm2 cmt3 double mutant and EMS-mutagenized lines wt #67, cmt3 #49, and cmt3 #7 plants showed strong GFP fluorescence. (B) Western blot using antibody against GFP (anti-GFP) confirms SDC::GFP overexpression in the EMS mutants. Coomassie staining of the large Rubisco subunit (rbcL) is used as loading control. (C) Number of TEs overexpressed in atmorc1 and atmorc6 mutants and classified by superfamily. For each mutant, only TEs with at least a fourfold increase in both the EMS and T-DNA alleles over wt and with a P ≤ 0.05 are represented. (D) Relative fold increase of four TE transcripts in atmorc1-4 and atmorc6-3 over wt assayed by real-time quantitative polymerase chain reaction (RT-qPCR) and normalized to ACTIN7. Errors bars indicate standard deviation based on three independent biological replicates.

We carried out ethyl methanesulfonate (EMS) mutagenesis screens in wild-type (wt) or cmt3 backgrounds for mutants showing SDC::GFP overexpression and identified the wt #67, cmt3 #7, and cmt3 #49 mutants (Fig. 1, A and B). Mapping experiments using bulk segregant analysis coupled to deep genome resequencing indicated that cmt3 #7 contained a mutation in At4g36290 (AtMORC1), previously also named COMPROMISED RECOGNITION OF TCV-1 (CRT1) (6, 7), whereas wt #67 and cmt3 #49 both contained mutations in At1g19100 (AtMORC6) (7) (figs. S1B, S2, and S3A). An atmorc1 allele was previously reported to show reduced resistance to the turnip crinkle virus (TCV) (6, 7), suggesting that AtMORC1 is involved in viral resistance in addition to its role in gene silencing described in this study, whereas mutations in AtMORC6 have not been described. To ensure that atmorc1 and atmorc6 mutations were those responsible for the loss of SDC silencing, we isolated knock-out transferred DNA (T-DNA) insertion lines atmorc1-4 and atmorc6-3 and confirmed SDC overexpression in these two mutant alleles (fig. S3, B to D). Genetic complementation crosses between the recessive EMS and T-DNA mutants confirmed AtMORC1 and AtMORC6 as the mutated genes responsible for SDC::GFP activation in the three EMS lines (fig. S3E). Therefore, #7, #67, and #49 were renamed atmorc1-3, atmorc6-1, and atmorc6-2, respectively.

By using RNA sequencing (RNA-seq) (8), we found that the majority of RNAs significantly affected in the atmorc1 and atmorc6 mutants showed up-regulation, and many of these were transposable elements (TEs) belonging to various transposon superfamilies, including, among others, the LTR/Gypsy, LTR/Copia, DNA/MuDR, and DNA/Harbinger families (Fig. 1, C and D; fig. S4A; table S1). The expression defects in the atmorc1 and atmorc6 mutants were very similar, with all but two of the transposons up-regulated in atmorc1 also up-regulated in atmorc6 (fig. S4B). Protein-coding genes overexpressed in the atmorc1 and atmorc6 EMS and T-DNA mutants included endogenous SDC (table S2). There was a high degree of overlap between the genes up-regulated in atmorc1 and atmorc6 (fig. S4C), most of them corresponding to DNA-methylated and silenced loci (fig. S4, D and E). We also performed RNA-seq in the atmorc1 atmorc6 double mutant and found a very similar set of genes and transposons up-regulated, with only a few genes up-regulated in the double mutant that were not up-regulated in each of the single mutants (table S3), suggesting that AtMORC1 and AtMORC6 may act together to enforce gene silencing.

Whole-genome bisulfite sequencing (BS-seq) (9) revealed that DNA methylation levels in all sequence contexts were unaltered in atmorc1 or atmorc6 relative to wild type at TEs up-regulated in atmorc1 or atmorc6 (Fig. 2, A and B), nor were there any bulk alterations in protein-coding genes or TEs in the genome (fig. S5, A and B). In addition, analyses at the pericentromeric satellite CEN180 repeats and five loci up-regulated in atmorc1 and atmorc6 showed that the DNA methylation patterns in atmorc1-4 and atmorc6-3 were similar to those of wild type (Fig. 2, C and D). Chromatin immunoprecipitation sequencing (ChIP-seq) analyses of H3K9me2 also did not reveal any changes in the atmorc1 or atmorc6 mutants at SDC or other up-regulated locations (fig. S6, A and B). Lastly, small RNA sequencing analyses showed that elements up-regulated in atmorc1 and atmorc6 mutants were enriched in small interfering RNAs (siRNAs), but these siRNA levels did not change in the mutants (fig. S7). Thus, AtMORC1 and AtMORC6 are not required to maintain DNA methylation, H3K9me2, or siRNAs, suggesting that AtMORC1 and AtMORC6 are likely to either act downstream of DNA methylation or enforce silencing by a novel mechanism.

Fig. 2

DNA methylation is not impaired in atmorc1 and atmorc6 mutants. (A and B) Metaplot analyses show DNA methylation level in atmorc1-4, atmorc6-3, and wt for the set of TEs up-regulated in atmorc1-4 (A) and atmorc6-3 (B). The gray vertical lines mark the boundaries between 1 kilobase upstream and downstream regions of TEs. (C) Southern blot analyses assayed CG methylation level at CEN180 repeats by using HpaII-treated genomic DNAs. m, methylated; u, unmethylated. met1-3 genomic DNA is used as positive control for loss of CG methylation (23). (D) Percent DNA methylation at SDC and four TEs overexpressed in atmorc1-4 and atmorc6-3 mutants assayed by bisulfite sequencing. Twenty-four clones were analyzed for each individual analysis.

AtMORC1 and AtMORC6 are homologs of mouse Microrchidia1 (MORC1) (10, 11) and contain gyrase, Hsp90, histidine kinase, and MutL (GHKL) and S5 domains, together comprising an adenosine triphosphatase (ATPase) module (6) in addition to a putative C-terminal coiled-coil domain (fig. S1B). The EMS mutations found in atmorc1-3, atmorc6-1, and atmorc6-2 alleles all introduced premature stop codons within the GHKL domain (fig. S1B).

Because of the similarity of AtMORC1 and AtMORC6 to ATPases involved in manipulating chromatin superstructure (12), these proteins may affect gene silencing through higher-order compaction of methylated and silent chromatin. In wild-type nuclei, pericentromeric heterochromatin forms densely staining nuclear bodies called chromocenters that localize to the nuclear periphery (13). We observed decondensation of chromocenters in the atmorc1 and atmorc6 mutants (as well as in atmorc1 atmorc6 double mutant) (figs. S8 to S11) and found that loci transcriptionally derepressed in the mutants mostly localized to pericentromeric heterochromatin (fig. S12 and tables S1 and S3). To directly examine whole-genome chromatin interactions, we performed Hi-C analyses in wild type and atmorc6-1 (14). Consistent with previous cytological studies (13), the wild-type genome showed interactions between telomeres as well as between euchromatic regions on the same chromosome arm (Fig. 3A). In contrast, pericentromeric heterochromatin regions interacted very weakly with the rest of the genome, consistent with their compaction in chromocenters (Fig. 3A). Although atmorc6-1 showed a roughly similar chromatin architecture (fig. S13), plotting the differences between mutant and wild type showed that atmorc6-1 shows an increase in interactions between the pericentromeric regions of all chromosomes with the euchromatic arms of all chromosomes and a corresponding depletion of interactions of euchromatic arms with themselves. Because the analysis reports relative changes with the sum of differences set to zero, the most likely interpretation of these findings is that pericentromeric regions interact more strongly with the euchromatic arms in atmorc6-1, although we cannot exclude that the mutant also has effects on the euchromatic arms (Fig. 3B). This interpretation is consistent with the cytological observations showing that chromocenters expand out into a larger area of the nucleus in the mutants (fig. S8). We also found, by using complementing myc-tagged transgenes, that AtMORC1 and AtMORC6 proteins formed small nuclear bodies that were usually adjacent to but not within chromocenters (Fig. 3C and figs. S14 and S15). These results are all consistent with a model in which AtMORC1 and AtMORC6 enforce compaction and gene silencing of pericentromeric heterochromatin, although it is also possible that changes in chromatin and gene expression in the mutant secondarily lead to the observed changes in chromatin compaction. Mutation of the plant-specific MOM1 gene has also been shown to affect gene silencing but not DNA methylation in Arabidopsis; however, mom1 mutants do not show chromocenter decondensation and therefore are likely to act via a different mechanism (15, 16).

Fig. 3

AtMORC1 and AtMORC6 are required for maintenance of chromatin architecture and form nuclear bodies near chromocenters, and morc-1 is involved in gene silencing in C. elegans. (A) Interaction matrix of the wt Arabidopsis genome from Hi-C analysis. Positions along the five chromosomes are shown from left to right and top to bottom, and each pixel represents interactions from uniquely mapping paired end reads in 200-kilobase bins. Black bars and circles mark the positions of the pericentromeric and telomeric regions, respectively. Light gray regions represent areas masked out because of problematic mapping. Black bars show separation between chromosomes. (B) Difference plot shows enrichment of Hi-C interactions in atmorc6-1 in red and interactions depleted in atmorc6-1 in blue. (C) Anti-Myc immunostaining showing localization of pAtMORC6::AtMORC6-Myc and pAtMORC1::AtMORC1-Myc in nuclear bodies adjacent to chromocenters. AtMORC1 and AtMORC6 showed 2.0 ± 1.0 (average ± standard deviation) and 2.5 ± 1.2 bodies per chromocenter, respectively. DAPI (4′,6-diamidino-2-phenylindole) staining shows chromocenter location. Bottom images are merges. (D) A silenced seam cell–specific GFP transgene in the eri-1 (mg366) sensitized background is overexpressed in worms fed with bacteria expressing double-stranded RNA targeting morc-1 or rde-4 but not in worms fed with bacteria expressing a control empty vector. Results are representative of five independent replicates.

A single MORC homolog, morc-1, is present in the worm Caenorhabditis elegans, which is devoid of DNA methylation (17). To test whether the C. elegans morc-1 (ZC155.3) is involved in gene silencing, we performed RNA interference (RNAi)–mediated knockdown of morc-1 in the eri-1 sensitized background, in which a GFP transgene is silenced in most of the worm seam cells (Fig. 3D) (18). morc-1–depleted worms showed GFP reactivation similar to worms depleted of rde-4, an essential component of gene silencing in C. elegans (Fig. 3D) (19). These results suggest that MORCs may play an ancient and conserved role in gene silencing. In addition, the observation that morc-1 is required for gene silencing in C. elegans reinforces our view that MORCs in Arabidopsis are enforcing silencing by a mechanism that may not be directly linked with DNA methylation. It is interesting to note that the phenotype of the Morc1-knockout mouse resembles Miwi2- and Dnmt3L-knockout mouse phenotypes, showing male-specific meiotic defects during spermatogenesis (10, 2022). Miwi2 and Dnmt3L are both required for TE silencing, and it is possible that Morc1 might be involved in transposon silencing in mammals as well. We propose that MORC family ATPases act to regulate chromatin architecture and gene silencing in a wide variety of eukaryotes.

Supplementary Materials

Materials and Methods

Figs. S1 to S15

Tables S1 to S4

References (2444)

References and Notes

  1. Acknowledgments: We thank M. Akhavan for sequencing, L. Goddard and L. Iruela-Arispe for assistance with confocal microscopy, and P. Fransz and I. Schubert for helpful discussions. S.F. is a Special Fellow of the Leukemia and Lymphoma Society. J.C. is supported by the Ruth L. Kirschstein National Research Service Award GM007185. R.P.M. is supported by the National Institute of General Medical Sciences (grant F32GM100617), and J.D. is supported by a W. M. Keck Foundation Distinguished Young Scholar in Medical Research Award. Research in the Jacobsen, Kim, Michaels, and Dekker laboratories was supported by NIH grants GM60398, GM088565, GM075060, and HG003143, respectively. Sequencing files have been deposited at Gene Expression Omnibus (GEO) (accession code GSE37644). The authors declare no competing financial interests. S.E.J. is an investigator of the Howard Hughes Medical Institute. Correspondence and requests for materials should be addressed to S.E.J.
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