Gaines William A, Godin Stephen K, Kabbinavar Faiz F, Rao Timsi, VanDemark Andrew P, Sung Patrick, Bernstein Kara A
Department of Molecular Biochemistry and Biophysics, Yale University School of Medicine, New Haven, Conneticut 06510, USA.
Department of Microbiology and Molecular Genetics, University of Pittsburgh School of Medicine, 5117 Centre Avenue, UPCI Research Pavilion, G5.c, Pittsburgh, Pennsylvania 15217, USA.
Nat Commun. 2015 Jul 28;6:7834. doi: 10.1038/ncomms8834.
The conserved budding yeast Rad51 paralogues, including Rad55, Rad57, Csm2 and Psy3 are indispensable for homologous recombination (HR)-mediated chromosome damage repair. Rad55 and Rad57 are associated in a heterodimer, while Csm2 and Psy3 form the Shu complex with Shu1 and Shu2. Here we show that Rad55 bridges an interaction between Csm2 with Rad51 and Rad52 and, using a fully reconstituted system, demonstrate that the Shu complex synergizes with Rad55-Rad57 and Rad52 to promote nucleation of Rad51 on single-stranded DNA pre-occupied by replication protein A (RPA). The csm2-F46A allele is unable to interact with Rad55, ablating the ability of the Shu complex to enhance Rad51 presynaptic filament assembly in vitro and impairing HR in vivo. Our results reveal that Rad55-Rad57, the Shu complex and Rad52 act as a functional ensemble to promote Rad51-filament assembly, which has important implications for understanding the role of the human RAD51 paralogues in Fanconi anaemia and cancer predisposition.
保守的芽殖酵母Rad51旁系同源物,包括Rad55、Rad57、Csm2和Psy3,对于同源重组(HR)介导的染色体损伤修复是不可或缺的。Rad55和Rad57以异二聚体形式结合,而Csm2和Psy3与Shu1和Shu2形成Shu复合体。在这里,我们表明Rad55在Csm2与Rad51和Rad52之间架起了相互作用的桥梁,并使用一个完全重构的系统证明,Shu复合体与Rad55-Rad57和Rad52协同作用,以促进Rad51在被复制蛋白A(RPA)占据的单链DNA上的成核。csm2-F46A等位基因无法与Rad55相互作用,从而消除了Shu复合体在体外增强Rad51突触前丝组装的能力,并在体内损害了同源重组。我们的结果表明,Rad55-Rad57、Shu复合体和Rad52作为一个功能整体,促进Rad51丝的组装,这对于理解人类RAD51旁系同源物在范可尼贫血和癌症易感性中的作用具有重要意义。