Tarsounas M, Moens P B
Department of Biology, York University, Toronto, Ontario, M3J 1P3 Canada.
Curr Top Dev Biol. 2001;51:109-34. doi: 10.1016/s0070-2153(01)51004-2.
Meiotic checkpoints are manifested through protein complexes capable of detecting an abnormality in chromosome metabolism and signaling it to effector molecules that subsequently delay or arrest the progression of meiosis. Some checkpoints act during the first meiotic prophase to monitor the repair of chromosomal DSBs, predominantly by meiotic recombination, or to ensure the correct establishment of synapsis and its well-timed dissolution. In mammals, a number of checkpoint and repair proteins localize to the meiotic chromosomal cores, sometimes in the context of the synaptonemal complex (SC). Here we discuss possible functions of these proteins in the accomplishment of meiotic recombination and normal progression of the meiotic pathway. Also, we present arguments for a structural role of cores and SCs in the assembly of the repair and checkpoint protein complexes on the chromosomes.
减数分裂检查点通过能够检测染色体代谢异常并将其信号传递给效应分子的蛋白质复合物表现出来,这些效应分子随后会延迟或阻止减数分裂的进程。一些检查点在第一次减数分裂前期发挥作用,主要通过减数分裂重组来监测染色体双链断裂(DSB)的修复,或确保联会的正确建立及其适时解体。在哺乳动物中,许多检查点和修复蛋白定位于减数分裂染色体核心,有时是在联会复合体(SC)的背景下。在这里,我们讨论这些蛋白质在完成减数分裂重组和减数分裂途径正常进程中的可能功能。此外,我们还提出了关于核心和SC在染色体上修复和检查点蛋白复合物组装中的结构作用的观点。