Du Hansen, Ishii Haruhiko, Pazin Michael J, Sen Ranjan
Laboratory of Cellular and Molecular Biology, National Institute on Aging, Baltimore, MD 21224, USA.
Mol Cell. 2008 Sep 5;31(5):641-9. doi: 10.1016/j.molcel.2008.08.012.
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.
(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。