| Literature DB >> 31399344 |
Jean-Pierre Etchegaray1, Lei Zhong2, Catherine Li2, Telmo Henriques3, Eileen Ablondi3, Tomoyoshi Nakadai4, Capucine Van Rechem2, Christina Ferrer2, Kenneth N Ross2, Jee-Eun Choi2, Ann Samarakkody5, Fei Ji6, Andrew Chang2, Ruslan I Sadreyev7, Sridhar Ramaswamy2, Sergei Nechaev5, Johnathan R Whetstine2, Robert G Roeder4, Karen Adelman3, Alon Goren8, Raul Mostoslavsky9.
Abstract
Transcriptional regulation in eukaryotes occurs at promoter-proximal regions wherein transcriptionally engaged RNA polymerase II (Pol II) pauses before proceeding toward productive elongation. The role of chromatin in pausing remains poorly understood. Here, we demonstrate that the histone deacetylase SIRT6 binds to Pol II and prevents the release of the negative elongation factor (NELF), thus stabilizing Pol II promoter-proximal pausing. Genetic depletion of SIRT6 or its chromatin deficiency upon glucose deprivation causes intragenic enrichment of acetylated histone H3 at lysines 9 (H3K9ac) and 56 (H3K56ac), activation of cyclin-dependent kinase 9 (CDK9)-that phosphorylates NELF and the carboxyl terminal domain of Pol II-and enrichment of the positive transcription elongation factors MYC, BRD4, PAF1, and the super elongation factors AFF4 and ELL2. These events lead to increased expression of genes involved in metabolism, protein synthesis, and embryonic development. Our results identified SIRT6 as a Pol II promoter-proximal pausing-dedicated histone deacetylase.Entities:
Keywords: BRD4; NELF; SIRT6; chromatin; epigenetics; histone deacetylation; transcription elongation; transcriptional pausing
Mesh:
Substances:
Year: 2019 PMID: 31399344 PMCID: PMC6907403 DOI: 10.1016/j.molcel.2019.06.034
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970