4.8 Article

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

出版社

NATL ACAD SCIENCES
DOI: 10.1073/pnas.1424228112

关键词

LDB1; ASCL1; MTA2; looping; enhancer

资金

  1. National Institutes of Health
  2. National Cancer Institute [DK018477, HL065445, NS034934, GM104459, DK039949, DK074868, CA173903, 5U24DK097748]
  3. Fonds de recherche du Quebec - Sante

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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 LIM interactor, interacting with 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.

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