| Literature DB >> 33631105 |
Isabel Regadas1, Olle Dahlberg1, Roshan Vaid1, Oanh Ho2, Sergey Belikov1, Gunjan Dixit3, Sebastian Deindl2, Jiayu Wen4, Mattias Mannervik5.
Abstract
Organismal development and cell differentiation critically depend on chromatin state transitions. However, certain developmentally regulated genes lack histone 3 lysine 9 and 27 acetylation (H3K9ac and H3K27ac, respectively) and histone 3 lysine 4 (H3K4) methylation, histone modifications common to most active genes. Here we describe a chromatin state featuring unique histone 3 lysine 14 acetylation (H3K14ac) peaks in key tissue-specific genes in Drosophila and human cells. Replacing H3K14 in Drosophila demonstrates that H3K14 is essential for expression of genes devoid of canonical histone modifications in the embryonic gut and larval wing imaginal disc, causing lethality and defective wing patterning. We find that the SWI/SNF protein Brahma (Brm) recognizes H3K14ac, that brm acts in the same genetic pathway as H3K14R, and that chromatin accessibility at H3K14ac-unique genes is decreased in H3K14R mutants. Our results show that acetylation of a single lysine is essential at genes devoid of canonical histone marks and uncover an important requirement for H3K14 in tissue-specific gene regulation.Entities:
Keywords: Brahma; Drosophila; SWI/SNF; chromatin state; developmental genomics; gene regulation; histone acetylation; mesenchymal stem cells
Year: 2021 PMID: 33631105 DOI: 10.1016/j.molcel.2021.01.041
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970