RAD51AP1通过增强RAD51重组酶促进同源重组和基因组稳定性。

Promotion of homologous recombination and genomic stability by RAD51AP1 via RAD51 recombinase enhancement.

作者信息

Wiese Claudia, Dray Eloïse, Groesser Torsten, San Filippo Joseph, Shi Idina, Collins David W, Tsai Miaw-Sheue, Williams Gareth J, Rydberg Bjorn, Sung Patrick, Schild David

机构信息

Life Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA.

出版信息

Mol Cell. 2007 Nov 9;28(3):482-90. doi: 10.1016/j.molcel.2007.08.027.

Abstract

Homologous recombination (HR) repairs chromosome damage and is indispensable for tumor suppression in humans. RAD51 mediates the DNA strand-pairing step in HR. RAD51 associated protein 1 (RAD51AP1) is a RAD51-interacting protein whose function has remained elusive. Knockdown of RAD51AP1 in human cells by RNA interference engenders sensitivity to different types of genotoxic stress, and RAD51AP1 is epistatic to the HR protein XRCC3. Moreover, RAD51AP1-depleted cells are impaired for the recombinational repair of a DNA double-strand break and exhibit chromatid breaks both spontaneously and upon DNA-damaging treatment. Purified RAD51AP1 binds both dsDNA and a D loop structure and, only when able to interact with RAD51, greatly stimulates the RAD51-mediated D loop reaction. Biochemical and cytological results show that RAD51AP1 functions at a step subsequent to the assembly of the RAD51-ssDNA nucleoprotein filament. Our findings provide evidence that RAD51AP1 helps maintain genomic integrity via RAD51 recombinase enhancement.

摘要

同源重组(HR)修复染色体损伤,对人类肿瘤抑制至关重要。RAD51介导HR中的DNA链配对步骤。RAD51相关蛋白1(RAD51AP1)是一种与RAD51相互作用的蛋白,其功能一直不明。通过RNA干扰在人类细胞中敲低RAD51AP1会导致对不同类型的基因毒性应激敏感,且RAD51AP1对HR蛋白XRCC3呈上位性。此外,RAD51AP1缺失的细胞在DNA双链断裂的重组修复方面存在缺陷,并且在自发状态以及DNA损伤处理后均表现出染色单体断裂。纯化的RAD51AP1既能结合双链DNA,也能结合D环结构,并且只有在能够与RAD51相互作用时,才会极大地刺激RAD51介导的D环反应。生化和细胞学结果表明,RAD51AP1在RAD51-单链DNA核蛋白丝组装之后的步骤发挥作用。我们的研究结果证明,RAD51AP1通过增强RAD51重组酶来帮助维持基因组完整性。

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