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V(D)J重排:重组酶复合物形成及DNA修复机制募集方面的最新见解

V(D)J Recombination: Recent Insights in Formation of the Recombinase Complex and Recruitment of DNA Repair Machinery.

作者信息

Christie Shaun M, Fijen Carel, Rothenberg Eli

机构信息

Department of Biochemistry and Molecular Pharmacology, NYU Grossman School of Medicine, New York, NY, United States.

出版信息

Front Cell Dev Biol. 2022 Apr 29;10:886718. doi: 10.3389/fcell.2022.886718. eCollection 2022.

Abstract

V(D)J recombination is an essential mechanism of the adaptive immune system, producing a diverse set of antigen receptors in developing lymphocytes via regulated double strand DNA break and subsequent repair. DNA cleavage is initiated by the recombinase complex, consisting of lymphocyte specific proteins RAG1 and RAG2, while the repair phase is completed by classical non-homologous end joining (NHEJ). Many of the individual steps of this process have been well described and new research has increased the scale to understand the mechanisms of initiation and intermediate stages of the pathway. In this review we discuss 1) the regulatory functions of RAGs, 2) recruitment of RAGs to the site of recombination and formation of a paired complex, 3) the transition from a post-cleavage complex containing RAGs and cleaved DNA ends to the NHEJ repair phase, and 4) the potential redundant roles of certain factors in repairing the break. Regulatory (non-core) domains of RAGs are not necessary for catalytic activity, but likely influence recruitment and stabilization through interaction with modified histones and conformational changes. To form long range paired complexes, recent studies have found evidence in support of large scale chromosomal contraction through various factors to utilize diverse gene segments. Following the paired cleavage event, four broken DNA ends must now make a regulated transition to the repair phase, which can be controlled by dynamic conformational changes and post-translational modification of the factors involved. Additionally, we examine the overlapping roles of certain NHEJ factors which allows for prevention of genomic instability due to incomplete repair in the absence of one, but are lethal in combined knockouts. To conclude, we focus on the importance of understanding the detail of these processes in regards to off-target recombination or deficiency-mediated clinical manifestations.

摘要

V(D)J重组是适应性免疫系统的一种基本机制,通过调控双链DNA断裂及随后的修复过程,在发育中的淋巴细胞中产生一系列多样的抗原受体。DNA切割由重组酶复合物启动,该复合物由淋巴细胞特异性蛋白RAG1和RAG2组成,而修复阶段则通过经典的非同源末端连接(NHEJ)完成。这一过程的许多具体步骤已得到充分描述,新的研究进一步拓展了我们对该途径起始和中间阶段机制的理解。在本综述中,我们将讨论:1)RAGs的调控功能;2)RAGs招募至重组位点并形成配对复合物;3)从包含RAGs和切割后DNA末端的切割后复合物向NHEJ修复阶段的转变;4)某些因子在修复断裂过程中可能存在的冗余作用。RAGs的调控(非核心)结构域对于催化活性并非必需,但可能通过与修饰组蛋白的相互作用和构象变化影响招募和稳定性。为了形成远距离配对复合物,最近的研究发现了通过各种因子支持大规模染色体收缩以利用不同基因片段的证据。在配对切割事件之后,四个断裂的DNA末端现在必须有调控地过渡到修复阶段,这可以通过相关因子的动态构象变化和翻译后修饰来控制。此外,我们研究了某些NHEJ因子的重叠作用,这些作用能够防止因缺少其中一个因子导致的不完全修复所引起的基因组不稳定,但在联合敲除时是致命的。总之,我们强调了解这些过程细节对于脱靶重组或缺陷介导的临床表现的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/264b/9099191/226450b826be/fcell-10-886718-g001.jpg

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