Robust Crossover Assurance and Regulated Interhomolog Access Maintain Meiotic Crossover Number

被引:96
|
作者
Rosu, Simona [1 ]
Libuda, Diana E. [2 ]
Villeneuve, Anne M. [1 ,2 ]
机构
[1] Stanford Univ, Sch Med, Dept Genet, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Dev Biol, Stanford, CA 94305 USA
关键词
DNA BREAK REPAIR; CROSSING-OVER; C-ELEGANS; MEIOSIS; RECOMBINATION; MECHANISM; INTERFERENCE; HOMEOSTASIS; SYNAPSIS;
D O I
10.1126/science.1212424
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
Most organisms rely on interhomolog crossovers (COs) to ensure proper meiotic chromosome segregation but make few COs per chromosome pair. By monitoring repair events at a defined double-strand break (DSB) site during Caenorhabditis elegans meiosis, we reveal mechanisms that ensure formation of the obligate CO while limiting CO number. We find that CO is the preferred DSB repair outcome in the absence of inhibitory effects of other (nascent) recombination events. Thus, a single DSB per chromosome pair is largely sufficient to ensure CO formation. Further, we show that access to the homolog as a repair template is regulated, shutting down simultaneously for both CO and noncrossover (NCO) pathways. We propose that regulation of interhomolog access limits CO number and contributes to CO interference.
引用
收藏
页码:1286 / 1289
页数:4
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