PRAKASH, Rohit, D. SATORY, E. DRAY, A. PAPUSHA, J. SCHELLER, W. KRAMER, Lumír KREJČÍ, Hannah KLEIN, J.E. HABER, Patrick SUNG and Grzegorz IRA. Yeast Mph1 helicase dissociates Rad51-made D-loops: implications for crossover control in mitotic recombination. Genes Dev. 2009, vol. 23, No 1, p. 67-79, 12 pp. ISSN 1549-5477.
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Basic information
Original name Yeast Mph1 helicase dissociates Rad51-made D-loops: implications for crossover control in mitotic recombination.
Name in Czech Kvasinková Mph1 helikáza potlačuje mitotické chromosomové crossovery
Authors PRAKASH, Rohit (840 United States of America), D. SATORY (840 United States of America), E. DRAY (840 United States of America), A. PAPUSHA (840 United States of America), J. SCHELLER (276 Germany), W. KRAMER (276 Germany), Lumír KREJČÍ (203 Czech Republic, guarantor), Hannah KLEIN (840 United States of America), J.E. HABER (840 United States of America), Patrick SUNG (840 United States of America) and Grzegorz IRA (840 United States of America).
Edition Genes Dev. 2009, 1549-5477.
Other information
Original language English
Type of outcome Article in a journal
Field of Study Genetics and molecular biology
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 12.075
RIV identification code RIV/00216224:14310/09:00029171
Organization unit Faculty of Science
UT WoS 000262369700007
Keywords in English Genome instability; recombination; DNA helicase; crossing over; Fanconi anemia
Tags crossing over, DNA helicase, Fanconi anemia, Genome instability, recombination
Tags International impact, Reviewed
Changed by Changed by: doc. Mgr. Lumír Krejčí, Ph.D., učo 18098. Changed: 1/7/2009 08:12.
Abstract
Eukaryotes possess mechanisms to limit crossing over during homologous recombination, thus avoiding possible chromosomal rearrangements. We show here that budding yeast Mph1, an ortholog of human FancM helicase, utilizes its helicase activity to suppress spontaneous unequal sister chromatid exchanges and DNA double-strand break-induced chromosome crossovers. Since the efficiency and kinetics of break repair are unaffected, Mph1 appears to channel repair intermediates into a noncrossover pathway. Importantly, Mph1 works independently of two other helicases-Srs2 and Sgs1-that also attenuate crossing over. By chromatin immunoprecipitation, we find targeting of Mph1 to double-strand breaks in cells. Purified Mph1 binds D-loop structures and is particularly adept at unwinding these structures. Importantly, Mph1, but not a helicase-defective variant, dissociates Rad51-made D-loops. Overall, the results from our analyses suggest a new role of Mph1 in promoting the noncrossover repair of DNA double-strand breaks.
Abstract (in Czech)
Eukaryotes possess mechanisms to limit crossing over during homologous recombination, thus avoiding possible chromosomal rearrangements. We show here that budding yeast Mph1, an ortholog of human FancM helicase, utilizes its helicase activity to suppress spontaneous unequal sister chromatid exchanges and DNA double-strand break-induced chromosome crossovers. Since the efficiency and kinetics of break repair are unaffected, Mph1 appears to channel repair intermediates into a noncrossover pathway. Importantly, Mph1 works independently of two other helicases-Srs2 and Sgs1-that also attenuate crossing over. By chromatin immunoprecipitation, we find targeting of Mph1 to double-strand breaks in cells. Purified Mph1 binds D-loop structures and is particularly adept at unwinding these structures. Importantly, Mph1, but not a helicase-defective variant, dissociates Rad51-made D-loops. Overall, the results from our analyses suggest a new role of Mph1 in promoting the noncrossover repair of DNA double-strand breaks.
Links
GA301/09/1917, research and development projectName: Štěpení replikačních-rekombinačních DNA meziproduktů a jejich úloha při nestabilitě genomu
Investor: Czech Science Foundation
GD203/09/H046, research and development projectName: Biochemie na rozcestí mezi in silico a in vitro
Investor: Czech Science Foundation
LC06030, research and development projectName: Biomolekulární centrum
Investor: Ministry of Education, Youth and Sports of the CR, Biomolecular centre
MSM0021622413, plan (intention)Name: Proteiny v metabolismu a při interakci organismů s prostředím
Investor: Ministry of Education, Youth and Sports of the CR, Proteins in metabolism and interaction of organisms with the environment
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