Mediator condensates localize signaling factors to key cell identity genes. Zamudio et al. S1

Main Author: Zamudio, Alicia
Format: Dataset
Terbitan: Mendeley , 2019
Subjects:
Online Access: https:/data.mendeley.com/datasets/99bt56v4zs
ctrlnum 0.17632-99bt56v4zs.1
fullrecord <?xml version="1.0"?> <dc><creator>Zamudio, Alicia</creator><title>Mediator condensates localize signaling factors to key cell identity genes. Zamudio et al. S1</title><publisher>Mendeley</publisher><description>The gene expression programs that define each cell&#x2019;s identity are controlled by master transcription factors (TFs) that bind cell-type specific enhancers, as well as signaling factors, which bring extracellular stimuli to these enhancers. Recent studies have revealed that master TFs form phase-separated condensates with the Mediator coactivator at super-enhancers. Here we present evidence that signaling factors for the WNT, TGF-&#x3B2; and JAK/STAT pathways employ their intrinsically disordered regions (IDRs) to enter and concentrate in Mediator condensates at super-enhancers. We show that the WNT coactivator &#x3B2;-catenin interacts both with components of condensates and DNA binding factors to selectively occupy super-enhancer associated genes. We propose that the cell-type specificity of the response to signaling is mediated, in part, by the IDRs of the signaling factors, which cause these factors to partition into condensates established by the master TFs and Mediator at genes with prominent roles in cell identity.</description><subject>Molecular Mechanism of Gene Regulation</subject><type>Other:Dataset</type><identifier>10.17632/99bt56v4zs.1</identifier><rights>Creative Commons Attribution 4.0 International</rights><rights>http://creativecommons.org/licenses/by/4.0</rights><relation>https:/data.mendeley.com/datasets/99bt56v4zs</relation><date>2019-09-16T17:58:57Z</date><date>2019-09-25T00:00:00Z</date><recordID>0.17632-99bt56v4zs.1</recordID></dc>
format Other:Dataset
Other
author Zamudio, Alicia
title Mediator condensates localize signaling factors to key cell identity genes. Zamudio et al. S1
publisher Mendeley
publishDate 2019
topic Molecular Mechanism of Gene Regulation
url https:/data.mendeley.com/datasets/99bt56v4zs
contents The gene expression programs that define each cell’s identity are controlled by master transcription factors (TFs) that bind cell-type specific enhancers, as well as signaling factors, which bring extracellular stimuli to these enhancers. Recent studies have revealed that master TFs form phase-separated condensates with the Mediator coactivator at super-enhancers. Here we present evidence that signaling factors for the WNT, TGF-β and JAK/STAT pathways employ their intrinsically disordered regions (IDRs) to enter and concentrate in Mediator condensates at super-enhancers. We show that the WNT coactivator β-catenin interacts both with components of condensates and DNA binding factors to selectively occupy super-enhancer associated genes. We propose that the cell-type specificity of the response to signaling is mediated, in part, by the IDRs of the signaling factors, which cause these factors to partition into condensates established by the master TFs and Mediator at genes with prominent roles in cell identity.
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