| Literature DB >> 28985501 |
Senthilkumar Cinghu1, Pengyi Yang1, Justin P Kosak1, Amanda E Conway1, Dhirendra Kumar1, Andrew J Oldfield1, Karen Adelman1, Raja Jothi2.
Abstract
Eukaryotic gene transcription is regulated at many steps, including RNA polymerase II (Pol II) recruitment, transcription initiation, promoter-proximal Pol II pause release, and transcription termination; however, mechanisms regulating transcription during productive elongation remain poorly understood. Enhancers, which activate gene transcription, themselves undergo Pol II-mediated transcription, but our understanding of enhancer transcription and enhancer RNAs (eRNAs) remains incomplete. Here we show that transcription at intragenic enhancers interferes with and attenuates host gene transcription during productive elongation. While the extent of attenuation correlates positively with nascent eRNA expression, the act of intragenic enhancer transcription alone, but not eRNAs, explains the attenuation. Through CRISPR/Cas9-mediated deletions, we demonstrate a physiological role for intragenic enhancer-mediated transcription attenuation in cell fate determination. We propose that intragenic enhancers not only enhance transcription of one or more genes from a distance but also fine-tune transcription of their host gene through transcription interference, facilitating differential utilization of the same regulatory element for disparate functions. Published by Elsevier Inc.Entities:
Keywords: enhancer; enhancer RNA; enhancer transcription; genetics; genomics; transcription regulation
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Year: 2017 PMID: 28985501 PMCID: PMC5683415 DOI: 10.1016/j.molcel.2017.09.010
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970