| Literature DB >> 30104406 |
Lian-Mei Tan1,2, Cui-Jun Zhang1, Xiao-Mei Hou1, Chang-Rong Shao1, Yu-Jia Lu1, Jin-Xing Zhou1, Yong-Qiang Li1, Lin Li1, She Chen1, Xin-Jian He3,2.
Abstract
In eukaryotes, heterochromatin regions are typically subjected to transcriptional silencing. DNA methylation has an important role in such silencing and has been studied extensively. However, little is known about how methylated heterochromatin regions are subjected to silencing. We conducted a genetic screen and identified an epcr (enhancer of polycomb-related) mutant that releases heterochromatin silencing in Arabidopsis thaliana We demonstrated that EPCR1 functions redundantly with its paralog EPCR2 and interacts with PWWP domain-containing proteins (PWWPs), AT-rich interaction domain-containing proteins (ARIDs), and telomere repeat binding proteins (TRBs), thus forming multiple functionally redundant protein complexes named PEAT (PWWPs-EPCRs-ARIDs-TRBs). The PEAT complexes mediate histone deacetylation and heterochromatin condensation and thereby facilitate heterochromatin silencing. In heterochromatin regions, the production of small interfering RNAs (siRNAs) and DNA methylation is repressed by the PEAT complexes. The study reveals how histone deacetylation, heterochromatin condensation, siRNA production, and DNA methylation interplay with each other and thereby maintain heterochromatin silencing.Entities:
Keywords: zzm321990EPLzzm321990; DNA methylation; PEAT complex; heterochromatin silencing; histone deacetylation; siRNA
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Year: 2018 PMID: 30104406 PMCID: PMC6166130 DOI: 10.15252/embj.201798770
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598