Saccharomyces cerevisiae MER3 helicase stimulates 3′-5′ Heteroduplex extension by Rad51:: Implications for crossover control in meiotic recombination

被引:84
作者
Mazina, OM
Mazin, AV
Nakagawa, T
Kolodner, RD
Kowalczykowski, SC [1 ]
机构
[1] Univ Calif Davis, Div Biol Sci, Microbiol Sect, Davis, CA 95616 USA
[2] Univ Calif Davis, Sect Mol & Cellular BIol, Ctr Genet & Dev, Davis, CA 95616 USA
[3] Drexel Univ, Coll Med, Dept Biochem, Philadelphia, PA 19102 USA
[4] Univ Calif San Diego, Sch Med, Ludwig Inst Canc Res, Ctr Canc, La Jolla, CA 92093 USA
[5] Univ Calif San Diego, Sch Med, Dept Med, La Jolla, CA 92093 USA
关键词
D O I
10.1016/S0092-8674(04)00294-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Crossover and noncrossover recombinants can form by two different pathways during meiotic recombination in Saccharomyces cerevisiae. The MER3 gene is known to affect selectively crossover, but not noncrossover, recombination. The Mer3 protein is a DNA helicase that unwinds duplex DNA in the 3' to 5' direction. To define the underlying molecular steps of meiotic recombination, we investigated the role of Mer3 helicase in DNA strand exchange promoted by Rad51 protein. We found that Mer3 helicase does not function as an initiator of DNA pairing events but, rather, it stimulates DNA heteroduplex extension in the 3' --> 5' direction relative to the incoming (or displaced) single-stranded DNA. Conversely, Mer3 helicase blocks DNA heteroduplex extension in the 5' --> 3' direction. Our results support the idea that Mer3 helicase stabilizes nascent joint molecules via DNA heteroduplex extension to permit capture of the second processed end of a double-stranded DNA break, a step which is required for crossover recombinant product formation.
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页码:47 / 56
页数:10
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