A meiotic recombination checkpoint controlled by mitotic checkpoint genes

被引:279
作者
Lydall, D
Nikolsky, Y
Bishop, DK
Weinert, T
机构
[1] UNIV ARIZONA,DEPT MOL & CELLULAR BIOL,TUCSON,AZ 85721
[2] UNIV CHICAGO,DEPT RADIAT & CELLULAR ONCOL,DEPT MOL GENET & CELL BIOL,CHICAGO,IL 60638
关键词
D O I
10.1038/383840a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
IN budding yeast, meiotic recombination occurs at about 200 sites per cell and involves DNA double-strand break (DSB) intermediates(1-3). Here we provide evidence that a checkpoint control requiring the mitotic DNA-damage checkpoint genes RAD17, RAD24 and MEC1 ensures that meiotic recombination is complete before the first meiotic division (MI). First, RAD17, RAD24 and MEC1 are required for the meiotic arrest caused by blocking the repair of DSBs with a mutation in the recA homologue DMC1. Second, mec1 and rad24 single mutants (DMC1(+)) appear to undergo MI before all recombination events are complete. Curiously, the mitosis-specific checkpoint gene RAD9 is not required for meiotic arrest of dmc1 mutants(4), This shows that although mitotic and meiotic control mechanisms are related, they differ significantly, Rad17 and Rad24 proteins may contribute directly to formation of an arrest signal by association with single-strand DNA in mitosis and meiosis.
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页码:840 / 843
页数:4
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