Department of Cellular and Molecular Medicine, University of California, San Diego, La Jolla, California 92093, USA; email:
Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, California 92093, USA.
Annu Rev Genet. 2021 Nov 23;55:497-526. doi: 10.1146/annurev-genet-071719-020235. Epub 2021 Sep 16.
The specialized two-stage meiotic cell division program halves a cell's chromosome complement in preparation for sexual reproduction. This reduction in ploidy requires that in meiotic prophase, each pair of homologous chromosomes (homologs) identify one another and form physical links through DNA recombination. Here, we review recent advances in understanding the complex morphological changes that chromosomes undergo during meiotic prophase to promote homolog identification and crossing over. We focus on the structural maintenance of chromosomes (SMC) family cohesin complexes and the meiotic chromosome axis, which together organize chromosomes and promote recombination. We then discuss the architecture and dynamics of the conserved synaptonemal complex (SC), which assembles between homologs and mediates local and global feedback to ensure high fidelity in meiotic recombination. Finally, we discuss exciting new advances, including mechanisms for boosting recombination on particular chromosomes or chromosomal domains and the implications of a new liquid crystal model for SC assembly and structure.
特化的两阶段减数分裂细胞分裂程序将细胞的染色体组减半,为有性繁殖做准备。这种倍性的减少要求在减数分裂前期,每一对同源染色体(同源染色体)相互识别,并通过 DNA 重组形成物理连接。在这里,我们回顾了近年来在理解染色体在减数分裂前期经历的复杂形态变化以促进同源染色体识别和交叉方面的进展。我们专注于结构维持染色体(SMC)家族黏合蛋白复合物和减数分裂染色体轴,它们共同组织染色体并促进重组。然后,我们讨论了保守联会复合体(SC)的结构和动力学,该复合体在同源染色体之间组装,并介导局部和全局反馈,以确保减数分裂重组的高保真度。最后,我们讨论了令人兴奋的新进展,包括在特定染色体或染色体区域上增强重组的机制,以及 SC 组装和结构的新液晶模型的意义。