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Enhancer-bound LDB1 regulates a corticotrope promoter-pausing repression program.

Authors :
Feng Zhang
Tanasa, Bogdan
Merkurjev, Daria
Chijen Lin
Xiaoyuan Song
Wenbo Li
Yuliang Tan
Zhijie Liu
Jie Zhang
Ohgi, Kenneth A.
Krones, Anna
Skowronska-Krawczyk, Dorota
Rosenfeld, Michael G.
Source :
Proceedings of the National Academy of Sciences of the United States of America. 2/3/2015, Vol. 112 Issue 5, p1380-1385. 6p.
Publication Year :
2015

Abstract

Substantial evidence supports the hypothesis that enhancers are critical regulators of cell-type determination, orchestrating both positive and negative transcriptional programs; however, the basic mechanisms by which enhancers orchestrate interactions with cognate promoters during activation and repression events remain incompletely understood. Here we report the required actions of LIM domain-binding protein 1 (LDB1)/cofactor of LIM homeodomain protein 2/nuclear LIMinteractor, interactingwith the enhancer-binding protein achaete-scute complex homolog 1, to mediate looping to target gene promoters and target gene regulation in corticotrope cells. LDB1-mediated enhancer:promoter looping appears to be required for both activation and repression of these target genes. Although LDB1-dependent activated genes are regulated at the level of transcriptional initiation, the LDB1-dependent repressed transcription units appear to be regulated primarily at the level of promoter pausing, with LDB1 regulating recruitment of metastasis-associated 1 family, member 2, a component of the nucleosome remodeling deacetylase complex, on these negative enhancers, required for the repressive enhancer function. These results indicate that LDB1-dependent looping events can deliver repressive cargo to cognate promoters to mediate promoter pausing events in a pituitary cell type. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00278424
Volume :
112
Issue :
5
Database :
Academic Search Index
Journal :
Proceedings of the National Academy of Sciences of the United States of America
Publication Type :
Academic Journal
Accession number :
103328192
Full Text :
https://doi.org/10.1073/pnas.1424228112