A novel protein, Rsf1/Pxd1, is critical for the single‐strand annealing pathway of double‐strand break repair in Schizosaccharomyces pombe. Issue 6 (11th April 2015)

• Record Type: Journal Article
• Authors: Wang, Hanqian; Zhang, Zhanlu; Zhang, Lan; Zhang, Qiuxue; Zhang, Liang; Zhao, Yangmin; Wang, Weibu; Fan, Yunliu; Wang, Lei
• Is Part Of: Molecular microbiology. Volume 96:Issue 6(2015)
• Page Start: 1211
• Page End: 1225
• Publication Date: 2015-04-11
• Subjects: Molecular microbiology -- Periodicals; 572.829
• DOI: 10.1111/mmi.13001
• Languages: English
• ISSNs: 0950-382X

Abstract

<abstract abstract-type="main"> <title>Summary</title> <p>The process of single‐strand annealing (SSA) repairs DNA double‐strand breaks that are flanked by direct repeat sequences through the coordinated actions of a series of proteins implicated in recombination, mismatch repair and nucleotide excision repair (NER). Many of the molecular and mechanistic insights gained in SSA repair have principally come from studies in the budding yeast <italic>S</italic><italic>accharomyces cerevisiae</italic>. However, there is little molecular understanding of the SSA pathway in the fission yeast <italic>S</italic><italic>chizosaccharomyces pombe</italic>. To further our understanding of this important process, we established a new chromosome‐based SSA assay in fission yeast. Our genetic analyses showed that, although many homologous components participate in SSA repair in these species indicating that some evolutionary conservation, Saw1 and Slx4 are not principal agents in the SSA repair pathway in fission yeast. This is in marked contrast to the function of Saw1 and Slx4 in budding yeast. Additionally, a novel genus‐specific protein, Rsf1/Pxd1, physically interacts with Rad16, Swi10 and Saw1 <italic>in vitro</italic> and <italic>in vivo</italic>. We find that Rsf1/Pxd1 is not required for NER and demonstrate that, in fission yeast, Rsf1/Pxd1, but not Saw1, plays a critical role in SSA recombination.</p> </abstract>