| Literature DB >> 31901448 |
Maria Ninova1, Baira Godneeva2, Yung-Chia Ariel Chen1, Yicheng Luo1, Sharan J Prakash1, Ferenc Jankovics3, Miklós Erdélyi3, Alexei A Aravin4, Katalin Fejes Tóth5.
Abstract
Сhromatin is critical for genome compaction and gene expression. On a coarse scale, the genome is divided into euchromatin, which harbors the majority of genes and is enriched in active chromatin marks, and heterochromatin, which is gene-poor but repeat-rich. The conserved molecular hallmark of heterochromatin is the H3K9me3 modification, which is associated with gene silencing. We found that in Drosophila, deposition of most of the H3K9me3 mark depends on SUMO and the SUMO ligase Su(var)2-10, which recruits the histone methyltransferase complex SetDB1/Wde. In addition to repressing repeats, H3K9me3 influences expression of both hetero- and euchromatic host genes. High H3K9me3 levels in heterochromatin are required to suppress spurious transcription and ensure proper gene expression. In euchromatin, a set of conserved genes is repressed by Su(var)2-10/SetDB1-induced H3K9 trimethylation, ensuring tissue-specific gene expression. Several components of heterochromatin are themselves repressed by this pathway, providing a negative feedback mechanism to ensure chromatin homeostasis.Entities:
Keywords: H3K9me3; SUMO; cell fate maintenance; chromatin; epigenetics; gene regulation; germline; heterochromatin; transcriptional repression; transposons
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Year: 2019 PMID: 31901448 PMCID: PMC7007874 DOI: 10.1016/j.molcel.2019.09.033
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970