Shetty Keerthi, Schatz David G
Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut, USA.
Department of Immunobiology, Yale University School of Medicine, New Haven, Connecticut, USA Howard Hughes Medical Institute, Yale University School of Medicine, New Haven, Connecticut, USA
Mol Cell Biol. 2015 Nov;35(21):3701-13. doi: 10.1128/MCB.00219-15. Epub 2015 Aug 24.
V(D)J recombination is initiated by the binding of the RAG1 and RAG2 proteins to recombination signal sequences (RSSs) that consist of conserved heptamer and nonamer sequences separated by a spacer of either 12 or 23 bp. Here, we used RAG-inducible pro-B v-Abl cell lines in conjunction with chromatin immunoprecipitation to better understand the protein and RSS requirements for RAG recruitment to chromatin. Using a catalytic mutant form of RAG1 to prevent recombination, we did not observe cooperation between RAG1 and RAG2 in their recruitment to endogenous Jκ gene segments over a 48-h time course. Using retroviral recombination substrates, we found that RAG1 was recruited inefficiently to substrates lacking an RSS or containing a single RSS, better to substrates with two 12-bp RSSs (12RSSs) or two 23-bp RSSs (23RSSs), and more efficiently to a substrate with a 12/23RSS pair. RSS mutagenesis demonstrated a major role for the nonamer element in RAG1 binding, and correspondingly, a cryptic RSS consisting of a repeat of CA dinucleotides, which poorly re-creates the nonamer, was ineffective in recruiting RAG1. Our findings suggest that 12RSS-23RSS cooperation (the "12/23 rule") is important not only for regulating RAG-mediated DNA cleavage but also for the efficiency of RAG recruitment to chromatin.
V(D)J重排是由RAG1和RAG2蛋白与重组信号序列(RSS)结合启动的,RSS由保守的七聚体和九聚体序列组成,中间间隔12或23个碱基对的间隔序列。在此,我们使用RAG诱导的前B细胞v-Abl细胞系结合染色质免疫沉淀技术,以更好地了解RAG募集到染色质上所需的蛋白质和RSS。使用RAG1的催化突变形式来阻止重排,在48小时的时间进程中,我们未观察到RAG1和RAG2在募集到内源性Jκ基因片段上存在协同作用。使用逆转录病毒重组底物,我们发现RAG1募集到缺乏RSS或含有单个RSS的底物上效率低下,募集到具有两个12碱基对RSS(12RSS)或两个23碱基对RSS(23RSS)的底物上效果较好,而募集到具有12/23 RSS对的底物上效率更高。RSS诱变表明九聚体元件在RAG1结合中起主要作用,相应地,由CA二核苷酸重复组成的隐蔽RSS由于很难重现九聚体,在募集RAG1方面无效。我们的研究结果表明,12RSS-23RSS协同作用(“12/23规则”)不仅对调节RAG介导的DNA切割很重要,而且对RAG募集到染色质的效率也很重要。