Abstract B099: Elucidating the mechanisms that underpin RAG chromatin scanning in V(D)J recombination at antigen receptor gene loci

Zhaoqing Ba, S. Jain, Jiazhi Hu, F. Alt
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引用次数: 0

Abstract

Immunoglobulin heavy (IgH) and light (IgL) chain variable region exons are assembled from V, D and J segments by V(D)J recombination, which is initiated by RAG1/RAG2 endonuclease (RAG) that introduces DNA double-stranded breaks (DSBs) between a pair of V, D, and J coding segments and flanking recombination signal sequences (RSSs). IgH V(D)J recombination is ordered, with D-JH joining occurring before appendage of a VH to a DJH intermediate in pro-B cells. In pre-B cells, a single-step VL-to-JL recombination event is invoked at IgL loci, with Ig kappa rearrangement usually preceding that of Ig lambda. The mechanisms of Ig V(D)J recombination, especially long-range VH-to-DJH and Vkappa-to-Jkappa recombination are still not fully understood. Recently, our work showed CTCF-binding elements (CBEs) immediately downstream of frequently rearranged VH-RSSs increase recombination potential of their associated VH far beyond that provided by RSS alone. This CBE activity becomes particularly striking upon the inactivation of IgH IGCR1 control element, which promotes DJH intermediate formation by insulting Ds, JHs, and recombination center (RC) from upstream VHs in a CBE-anchored chromatin loop. By developing and applying 3C-HTGTS, a new high-throughput chromosome conformation capture method that shows great advantages over classical 4C-seq in sensitivity and specificity, we found VH-associated CBEs promotes interaction with the RC. Based on these, we proposed a RAG chromatin scanning model for V(D)J recombination, in which VH CBEs stabilize interactions of D-proximal VHs first encountered by the DJH RC during linear RAG scanning on chromatin and thereby promote dominant rearrangement of these VHs by an unanticipated chromatin accessibility-enhancing CBE function. However, it is still not known if such chromatin scanning also happens on other antigen receptor loci and what the underlying mechanism is. Here, we will show our new findings on the roles of RAG chromatin scanning in Vkappa-to-Jkappa recombination at Ig kappa locus by multiple comprehensive approaches. Moreover, we will also discuss our most updated understanding of the mechanisms underlying RAG chromatin scanning using a novel and sophisticated approach. The potent mutagenic and oncogenic effects of aberrant RAG chromatin scanning at RAG “off-target” sites genome-wide will be also discussed. Citation Format: Zhaoqing Ba, Suvi Jain, Jiazhi Hu, Frederick Alt. Elucidating the mechanisms that underpin RAG chromatin scanning in V(D)J recombination at antigen receptor gene loci [abstract]. In: Proceedings of the Fourth CRI-CIMT-EATI-AACR International Cancer Immunotherapy Conference: Translating Science into Survival; Sept 30-Oct 3, 2018; New York, NY. Philadelphia (PA): AACR; Cancer Immunol Res 2019;7(2 Suppl):Abstract nr B099.
B099:阐明抗原受体基因位点V(D)J重组中RAG染色质扫描的机制
免疫球蛋白重链(IgH)和轻链(IgL)可变区外显子通过V(D)J重组从V、D和J段组装而成,V(D)J重组由RAG1/RAG2核酸内切酶(RAG)启动,在一对V、D和J编码段和侧翼重组信号序列(rss)之间引入DNA双链断裂(DSBs)。在前b细胞中,IgH - V(D)J重组是有序的,D- jh连接发生在VH附着到DJH中间体之前。在前b细胞中,IgL位点触发了一个单步的VL-to-JL重组事件,Ig kappa重排通常先于Ig lambda重排。Ig V(D)J重组的机制,特别是vh - djh和vkappa - jkappa的远程重组机制尚不完全清楚。最近,我们的研究表明,经常重排的VH-RSS下游的ctcf结合元件(CBEs)增加了其相关VH的重组潜力,远远超过RSS单独提供的潜力。这种CBE活性在IgH IGCR1控制元件失活时变得特别突出,该元件通过在CBE锚定的染色质环中从上游VHs中破坏Ds、JHs和重组中心(RC)来促进DJH中间产物的形成。通过开发和应用一种新的高通量染色体构象捕获方法3C-HTGTS,我们发现vh相关的CBEs促进了与RC的相互作用,这种方法在敏感性和特异性上都优于经典的4C-seq。基于此,我们提出了一个用于V(D)J重组的RAG染色质扫描模型,其中VH CBE稳定了DJH RC在染色质线性RAG扫描期间首次遇到的D-近端VHs的相互作用,从而通过意想不到的染色质可及性增强CBE功能促进了这些VHs的显性重排。然而,目前尚不清楚这种染色质扫描是否也发生在其他抗原受体位点上,以及其潜在的机制是什么。在这里,我们将通过多种综合方法展示RAG染色质扫描在Ig kappa位点vkappa - jkappa重组中的作用的新发现。此外,我们还将使用一种新颖而复杂的方法讨论我们对RAG染色质扫描机制的最新理解。还将讨论在全基因组范围内RAG“脱靶”位点进行异常RAG染色质扫描的强致突变和致癌作用。引用本文:巴肇庆,Suvi Jain,胡嘉志,Frederick Alt.抗原受体基因位点V(D)J重组中RAG染色质扫描的机制研究[摘要]。第四届CRI-CIMT-EATI-AACR国际癌症免疫治疗会议:将科学转化为生存;2018年9月30日至10月3日;纽约,纽约。费城(PA): AACR;癌症免疫学杂志,2019;7(2增刊):摘要nr B099。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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