| Literature DB >> 34375584 |
Xiaoyi Wang1, Joao A Paulo2, Xue Li3, Haining Zhou1, Juntao Yu1, Steven P Gygi2, Danesh Moazed4.
Abstract
Epigenetic inheritance of heterochromatin requires DNA-sequence-independent propagation mechanisms, coupling to RNAi, or input from DNA sequence, but how DNA contributes to inheritance is not understood. Here, we identify a DNA element (termed "maintainer") that is sufficient for epigenetic inheritance of pre-existing histone H3 lysine 9 methylation (H3K9me) and heterochromatin in Schizosaccharomyces pombe but cannot establish de novo gene silencing in wild-type cells. This maintainer is a composite DNA element with binding sites for the Atf1/Pcr1 and Deb1 transcription factors and the origin recognition complex (ORC), located within a 130-bp region, and can be converted to a silencer in cells with lower rates of H3K9me turnover, suggesting that it participates in recruiting the H3K9 methyltransferase Clr4/Suv39h. These results suggest that, in the absence of RNAi, histone H3K9me is only heritable when it can collaborate with maintainer-associated DNA-binding proteins that help recruit the enzyme responsible for its epigenetic deposition.Entities:
Keywords: Atf1; Clr4; Deb1; H3K9me; ORC; Pcr1; Suv39h; epigenetic inheritance; heterochromatin; maintainer
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Year: 2021 PMID: 34375584 PMCID: PMC8500937 DOI: 10.1016/j.molcel.2021.07.017
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 19.328