Srs2 promotes Mus81-Mms4-mediated resolution of recombination intermediates

• Published in: Nucleic acids research Vol. 43; no. 7; pp. 3626 - 3642
• Main Authors: Chavdarova, Melita, Marini, Victoria, Sisakova, Alexandra, Sedlackova, Hana, Vigasova, Dana, Brill, Steven J, Lisby, Michael, Krejci, Lumir
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 20.04.2015
• Subjects: Base Sequence; DNA Helicases - physiology; DNA Primers; DNA-Binding Proteins - physiology; Endonucleases - physiology; Flap Endonucleases - physiology; Genome Integrity, Repair and; Microscopy, Fluorescence; Polymerase Chain Reaction; Recombination, Genetic; Saccharomyces cerevisiae - metabolism; Saccharomyces cerevisiae Proteins - physiology; Two-Hybrid System Techniques
• ISSN: 0305-1048; 1362-4962
• DOI: 10.1093/nar/gkv198

A variety of DNA lesions, secondary DNA structures or topological stress within the DNA template may lead to stalling of the replication fork. Recovery of such forks is essential for the maintenance of genomic stability. The structure-specific endonuclease Mus81-Mms4 has been implicated in processing DNA intermediates that arise from collapsed forks and homologous recombination. According to previous genetic studies, the Srs2 helicase may play a role in the repair of double-strand breaks and ssDNA gaps together with Mus81-Mms4. In this study, we show that the Srs2 and Mus81-Mms4 proteins physically interact in vitro and in vivo and we map the interaction domains within the Srs2 and Mus81 proteins. Further, we show that Srs2 plays a dual role in the stimulation of the Mus81-Mms4 nuclease activity on a variety of DNA substrates. First, Srs2 directly stimulates Mus81-Mms4 nuclease activity independent of its helicase activity. Second, Srs2 removes Rad51 from DNA to allow access of Mus81-Mms4 to cleave DNA. Concomitantly, Mus81-Mms4 inhibits the helicase activity of Srs2. Taken together, our data point to a coordinated role of Mus81-Mms4 and Srs2 in processing of recombination as well as replication intermediates.