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启动子/增强子全复合物对TCRβ基因组装的调控

Regulation of TCRbeta gene assembly by a promoter/enhancer holocomplex.

作者信息

Oestreich Kenneth J, Cobb Robin Milley, Pierce Steven, Chen Jianzhu, Ferrier Pierre, Oltz Eugene M

机构信息

Department of Microbiology and Immunology, Vanderbilt University, Nashville, Tennessee 37232, USA.

出版信息

Immunity. 2006 Apr;24(4):381-91. doi: 10.1016/j.immuni.2006.02.009.

Abstract

Antigen receptor gene assembly is governed by transcriptional promoters and enhancers that communicate over large distances and modulate chromatin accessibility to V(D)J recombinase. The precise role of these cis-acting elements in opening chromatin at recombinase targets and the mechanisms underlying their crosstalk remain unclear. We show that the TCRbeta enhancer (Ebeta) directs long-range chromatin opening over both DbetaJbeta clusters. Strikingly, chromatin associated with the Dbeta1 gene segment is refractory to Ebeta-mediated opening. Accessibility at Dbeta1 is accompanied by the formation of a stable holocomplex between a Dbeta-proximal promoter and Ebeta. These findings indicate a stepwise process for Dbeta --> Jbeta recombination that relies on distinct aspects of Ebeta activity: an intrinsic function that directs general chromatin opening and a cooperative function that facilitates the assembly of a promoter/enhancer holocomplex, unmasks the Dbeta1 gene segment, and triggers TCRbeta gene assembly.

摘要

抗原受体基因组装受转录启动子和增强子调控,这些元件可远距离通讯并调节染色质对V(D)J重组酶的可及性。这些顺式作用元件在重组酶靶点处打开染色质的确切作用及其相互作用的机制仍不清楚。我们发现TCRβ增强子(Eβ)指导跨越两个DβJβ簇的远距离染色质开放。令人惊讶的是,与Dβ1基因片段相关的染色质对Eβ介导的开放具有抗性。Dβ1处的可及性伴随着Dβ近端启动子与Eβ之间形成稳定的全复合物。这些发现表明Dβ→Jβ重组是一个逐步的过程,依赖于Eβ活性的不同方面:指导一般染色质开放的内在功能和促进启动子/增强子全复合物组装、暴露Dβ1基因片段并触发TCRβ基因组装的协同功能。

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