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在无转录情况下,hSWI/SNF复合物对12/23-RSS依赖性RAG切割的激活作用。

Activation of 12/23-RSS-dependent RAG cleavage by hSWI/SNF complex in the absence of transcription.

作者信息

Du Hansen, Ishii Haruhiko, Pazin Michael J, Sen Ranjan

机构信息

Laboratory of Cellular and Molecular Biology, National Institute on Aging, Baltimore, MD 21224, USA.

出版信息

Mol Cell. 2008 Sep 5;31(5):641-9. doi: 10.1016/j.molcel.2008.08.012.

Abstract

Maintenance of genomic integrity during antigen receptor gene rearrangements requires (1) regulated access of the V(D)J recombinase to specific loci and (2) generation of double-strand DNA breaks only after recognition of a pair of matched recombination signal sequences (RSSs). Here we recapitulate both key aspects of regulated recombinase accessibility in a cell-free system using plasmid substrates assembled into chromatin. We show that recruitment of the SWI/SNF chromatin-remodeling complex to both RSSs increases coupled cleavage by RAG1 and RAG2 proteins. SWI/SNF functions by altering local chromatin structure in the absence of RNA polymerase II-dependent transcription or histone modifications. These observations demonstrate a direct role for cis-sequence-regulated local chromatin remodeling in RAG1/2-dependent initiation of V(D)J recombination.

摘要

在抗原受体基因重排过程中维持基因组完整性需要

(1)V(D)J重组酶有调控地接近特定基因座;(2)仅在识别一对匹配的重组信号序列(RSS)后才产生双链DNA断裂。在这里,我们使用组装成染色质的质粒底物,在无细胞系统中重现了重组酶可及性调控的两个关键方面。我们表明,SWI/SNF染色质重塑复合物被募集到两个RSS上会增加RAG1和RAG2蛋白的偶联切割。在没有RNA聚合酶II依赖性转录或组蛋白修饰的情况下,SWI/SNF通过改变局部染色质结构发挥作用。这些观察结果证明了顺式序列调控的局部染色质重塑在RAG1/2依赖性V(D)J重组起始中的直接作用。

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