Department of Genetics, Stanford University School of Medicine, Stanford, CA 94305, USA.
Science. 2011 Dec 2;334(6060):1286-9. doi: 10.1126/science.1212424.
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.
大多数生物体依赖于同源重组交叉(COs)来确保减数分裂染色体的正确分离,但每个染色体对只产生很少的 COs。通过在秀丽隐杆线虫减数分裂过程中监测特定双链断裂(DSB)位点的修复事件,我们揭示了确保必需的 CO 形成同时限制 CO 数量的机制。我们发现,在不存在其他(新生)重组事件抑制效应的情况下,CO 是 DSB 修复的首选结果。因此,每个染色体对的单个 DSB 基本上足以确保 CO 的形成。此外,我们表明,同源作为修复模板的访问受到调控,同时关闭 CO 和非交叉(NCO)途径。我们提出,同源访问的调控限制了 CO 的数量,并有助于 CO 干扰。