In plants and mammals, DNA methylation plays a critical role in transcriptional silencing by delineating heterochromatin from transcriptionally active euchromatin. A homeostatic balance between heterochromatin and euchromatin is essential to genomic stability. This is evident in many diseases and mutants for heterochromatin maintenance, which are characterized by global losses of DNA methylation coupled with localized ectopic gains of DNA methylation that alter transcription. Furthermore, we have shown that genome-wide methylation patterns inArabidopsis thalianaare highly stable over generations, with the exception of rare epialleles. However, the extent to which natural variation in the robustness of targeting DNA methylation to heterochromatin exists, and the phenotypic consequences of such variation, remain to be fully explored. Here we describe the finding that heterochromatin and genic DNA methylation are highly variable among 725A. thalianaaccessions. We found that genic DNA methylation is inversely correlated with that in heterochromatin, suggesting that certain methylation pathway(s) may be redirected to genes upon the loss of heterochromatin. This redistribution likely involves a feedback loop involving the DNA methyltransferase, CHROMOMETHYLASE 3 (CMT3), H3K9me2, and histone turnover, as highly expressed, long genes with a high density of CMT3-preferred CWG sites are more likely to be methylated. Importantly, although the presence of CG methylation in genes alone may not affect transcription, genes containing CG methylation are more likely to become methylated at non-CG sites and silenced. These findings are consistent with the hypothesis that natural variation in DNA methylation homeostasis may underlie the evolution of epialleles that alter phenotypes.
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DNA methyltransferase CHROMOMETHYLASE3 prevents ONSEN transposon silencing under heat stress
DNA methylation plays crucial roles in transposon silencing and genome integrity. CHROMOMETHYLASE3 (CMT3) is a plant-specific DNA methyltransferase responsible for catalyzing DNA methylation at the CHG (H = A, T, C) context. Here, we identified a positive role of CMT3 in heat-induced activation of retrotransposonONSEN. We found that the full transcription ofONSENunder heat stress requires CMT3. Interestingly, loss-of-function CMT3 mutation led to increased CHH methylation atONSEN. The CHH methylation is mediated by CMT2, as evidenced by greatly reduced CHH methylation incmt2andcmt2 cmt3mutants coupled with increasedONSENtranscription. Furthermore, we found more CMT2 binding atONSENchromatin incmt3compared to wild-type accompanied with an ectopic accumulation of H3K9me2 under heat stress, suggesting a collaborative role of H3K9me2 and CHH methylation in preventing heat-inducedONSENactivation. In summary, this study identifies a non-canonical role of CMT3 in preventing transposon silencing and provides new insights into how DNA methyltransferases regulate transcription under stress conditions.
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- PAR ID:
- 10485382
- Editor(s):
- Springer, Nathan M.
- Publisher / Repository:
- A nonprofit publisher of open-access journal
- Date Published:
- Journal Name:
- PLOS Genetics
- Volume:
- 17
- Issue:
- 8
- ISSN:
- 1553-7404
- Page Range / eLocation ID:
- e1009710
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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