BCLAF1是BACH1的功能伴侣,参与DNA损伤应答

IF 3 3区 生物学 Q2 GENETICS & HEREDITY DNA Repair Pub Date : 2022-10-01 DOI:10.1016/j.dnarep.2022.103371
Kai Jiang , Yuanyuan Ding , Changjiang Dong , Feifei Shan , Kun Guo , Jiwang Zhang , Feng Zhang
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引用次数: 1

摘要

BACH1 (Brca1-Associated C-terminal Helicase)是一种重要的DNA损伤应答因子,参与DNA损伤修复和基因组稳定性的维持。在本研究中,通过串联蛋白亲和纯化,我们鉴定出BCLAF1是BACH1的一个新的功能伙伴。无论DNA损伤如何,BCLAF1都能与BACH1相互作用。然而,在对DNA损伤的反应中,BCLAF1与BACH1一起被招募到DNA损伤位点,BCLAF1的招募受BACH1和BRCA1的调节。有趣的是,BCLAF1缺陷细胞缺乏dsb启动的HR,但RAD51病灶形成在IR治疗后是完整的。综上所述,这些发现表明BCLAF1是BACH1的功能性结合伙伴,在DNA损伤反应中起关键作用。
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BCLAF1, a functional partner of BACH1, participates in DNA damage response

BACH1 (Brca1-Associated C-terminal Helicase) is an important DNA damage response factor, which is involved in DNA damage repair and maintenance of genomic stability. In this study, by using tandem protein affinity purification, we have identified BCLAF1 as a novel functional partner of BACH1. BCLAF1 constitutively interacts with BACH1 regardless of DNA damage. However, in response to DNA damage, along with BACH1, BCLAF1 is recruited to the DNA damage sites and the recruitment of BCLAF1 was regulated by BACH1 and BRCA1. Interestingly, BCLAF1 deficient cells are deficient for DSB-initiated HR, but RAD51 foci formation is intact following IR treatment. Taken together, these findings reveal that BCLAF1 is a functional binding partner of BACH1 playing a key role in DNA damage response.

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来源期刊
DNA Repair
DNA Repair 生物-毒理学
CiteScore
7.60
自引率
5.30%
发文量
91
审稿时长
59 days
期刊介绍: DNA Repair provides a forum for the comprehensive coverage of DNA repair and cellular responses to DNA damage. The journal publishes original observations on genetic, cellular, biochemical, structural and molecular aspects of DNA repair, mutagenesis, cell cycle regulation, apoptosis and other biological responses in cells exposed to genomic insult, as well as their relationship to human disease. DNA Repair publishes full-length research articles, brief reports on research, and reviews. The journal welcomes articles describing databases, methods and new technologies supporting research on DNA repair and responses to DNA damage. Letters to the Editor, hot topics and classics in DNA repair, historical reflections, book reviews and meeting reports also will be considered for publication.
期刊最新文献
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