| Literature DB >> 29920280 |
Zeyang Ma1, Claudia Castillo-González1, Zhiye Wang1, Di Sun1, Xiaomei Hu1, Xuefeng Shen2, Magdalena E Potok3, Xiuren Zhang4.
Abstract
Serrate (SE) is a key component in RNA metabolism. Little is known about whether and how it can regulate epigenetic silencing. Here, we report histone methyltransferases ATXR5 and ATXR6 (ATXR5/6) as novel partners of SE. ATXR5/6 deposit histone 3 lysine 27 monomethylation (H3K27me1) to promote heterochromatin formation, repress transposable elements (TEs), and control genome stability in Arabidopsis. SE binds to ATXR5/6-regulated TE loci and promotes H3K27me1 accumulation in these regions. Furthermore, SE directly enhances ATXR5 enzymatic activity in vitro. Unexpectedly, se mutation suppresses the TE reactivation and DNA re-replication phenotypes in the atxr5 atxr6 mutant. The suppression of TE expression results from triggering RNA-dependent RNA polymerase 6 (RDR6)-dependent RNA silencing in the se atxr5 atxr6 mutant. We propose that SE facilitates ATXR5/6-mediated deposition of the H3K27me1 mark while inhibiting RDR6-mediated RNA silencing to protect TE transcripts. Hence, SE coordinates epigenetic silencing and RNA processing machineries to fine-tune the TE expression.Entities:
Keywords: RNA silencing; chromatin modification; epigenetic; gene expression; histone methylation
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Year: 2018 PMID: 29920280 DOI: 10.1016/j.devcel.2018.05.023
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270