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Mol Cell DOI:10.1016/j.molcel.2019.06.034

The Histone Deacetylase SIRT6 Restrains Transcription Elongation via Promoter-Proximal Pausing.

Publication TypeJournal Article
Year of Publication2019
AuthorsEtchegaray, J-P, Zhong, L, Li, C, Henriques, T, Ablondi, E, Nakadai, T, Van Rechem, C, Ferrer, C, Ross, KN, Choi, J-E, Samarakkody, A, Ji, F, Chang, A, Sadreyev, RI, Ramaswamy, S, Nechaev, S, Whetstine, JR, Roeder, RG, Adelman, K, Goren, A, Mostoslavsky, R
JournalMol Cell
Volume75
Issue4
Pages683-699.e7
Date Published2019 Aug 22
ISSN1097-4164
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.

DOI10.1016/j.molcel.2019.06.034
Pubmed

http://www.ncbi.nlm.nih.gov/pubmed/31399344?dopt=Abstract

Alternate JournalMol. Cell
PubMed ID31399344