Literature DB >> 31563432

Mediator Condensates Localize Signaling Factors to Key Cell Identity Genes.

Alicia V Zamudio1, Alessandra Dall'Agnese2, Jonathan E Henninger2, John C Manteiga1, Lena K Afeyan1, Nancy M Hannett2, Eliot L Coffey1, Charles H Li1, Ozgur Oksuz2, Benjamin R Sabari2, Ann Boija2, Isaac A Klein3, Susana W Hawken4, Jan-Hendrik Spille5, Tim-Michael Decker6, Ibrahim I Cisse5, Brian J Abraham7, Tong I Lee2, Dylan J Taatjes6, Jurian Schuijers8, Richard A Young9.   

Abstract

The gene expression programs that define the identity of each cell 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 use 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.
Copyright © 2019 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  JAK/STAT; TGF-β; WNT; gene regulation; signaling pathway; transcriptional condensates

Mesh:

Substances:

Year:  2019        PMID: 31563432      PMCID: PMC6898777          DOI: 10.1016/j.molcel.2019.08.016

Source DB:  PubMed          Journal:  Mol Cell        ISSN: 1097-2765            Impact factor:   17.970


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