Zhang Feng, Tanasa Bogdan, Merkurjev Daria, Lin Chijen, Song Xiaoyuan, Li Wenbo, Tan Yuliang, Liu Zhijie, Zhang Jie, Ohgi Kenneth A, Krones Anna, Skowronska-Krawczyk Dorota, Rosenfeld Michael G
Howard Hughes Medical Institute and Department of Medicine, School of Medicine,
Howard Hughes Medical Institute and Department of Medicine, School of Medicine.
Proc Natl Acad Sci U S A. 2015 Feb 3;112(5):1380-5. doi: 10.1073/pnas.1424228112. Epub 2015 Jan 20.
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.
增强子是细胞类型决定的关键调节因子,协调正负转录程序;然而,增强子在激活和抑制事件中协调与同源启动子相互作用的基本机制仍未完全了解。在这里,我们报告了LIM结构域结合蛋白1(LDB1)/LIM同源结构域蛋白2的辅因子/核LIM相互作用因子的必要作用,其与增强子结合蛋白无翅型MMTV整合位点家族成员1相互作用,以介导与促肾上腺皮质激素细胞中靶基因启动子的环化及靶基因调控。LDB1介导的增强子:启动子环化似乎是这些靶基因激活和抑制所必需的。虽然依赖LDB1的激活基因在转录起始水平受到调控,但依赖LDB1的抑制转录单元似乎主要在启动子暂停水平受到调控,LDB1在这些负增强子上调节转移相关蛋白1家族成员2(核小体重塑去乙酰化酶复合体的一个组分)的募集,这是抑制性增强子功能所必需的。这些结果表明,依赖LDB1的环化事件可将抑制性物质传递至同源启动子,以介导垂体细胞类型中的启动子暂停事件。