Hochwagen Andreas, Amon Angelika
Center for Cancer Research and Howard Hughes Medical Institute, Massachusetts Institute of Technology, E17-233, 40 Ames Street, Cambridge Massachusetts 02139, USA.
Curr Biol. 2006 Mar 21;16(6):R217-28. doi: 10.1016/j.cub.2006.03.009.
Numerous DNA double-strand breaks (DSBs) are introduced into the genome in the course of meiotic recombination. This poses a significant hazard to the genomic integrity of the cell. Studies in a number of organisms have unveiled the existence of surveillance mechanisms or checkpoints that couple the formation and repair of DSBs to cell cycle progression. Through these mechanisms, aberrant meiocytes are delayed in their meiotic progression, thereby facilitating repair of meiotic DSBs, or are culled through programmed cell death, thereby protecting the germline from aneuploidies that could lead to spontaneous abortions, birth defects and cancer predisposition in the offspring. Here we summarize recent progress in our understanding of these checkpoints. This review focuses on the surveillance mechanisms of the budding yeast S. cerevisiae, where the molecular details are best understood, but will frequently compare and contrast these mechanisms with observations in other organisms.
在减数分裂重组过程中,基因组会产生大量DNA双链断裂(DSB)。这对细胞的基因组完整性构成了重大威胁。对多种生物体的研究揭示了存在一些监测机制或检查点,这些机制将DSB的形成和修复与细胞周期进程联系起来。通过这些机制,异常的减数分裂细胞在减数分裂进程中被延迟,从而促进减数分裂DSB的修复,或者通过程序性细胞死亡被剔除,从而保护种系免受可能导致后代自然流产、出生缺陷和癌症易感性的非整倍体影响。在此,我们总结了我们对这些检查点理解的最新进展。本综述重点关注芽殖酵母酿酒酵母的监测机制,其分子细节最为清楚,但也会经常将这些机制与其他生物体中的观察结果进行比较和对比。