Centro de Investigaciones Biológicas (CIB-CSIC), Calle Ramiro de Maeztu 928040 Madrid, Spain.
Bioessays. 2018 Oct;40(10):e1800109. doi: 10.1002/bies.201800109. Epub 2018 Aug 14.
Cohesion is established in S-phase through the action of key replisome factors as replication forks engage cohesin molecules. By holding sister chromatids together, cohesion critically assists both an equal segregation of the duplicated genetic material and an efficient repair of DNA breaks. Nonetheless, the molecular events leading the entrapment of nascent chromatids by cohesin during replication are only beginning to be understood. The authors describe here the essential structural features of the cohesin complex in connection to its ability to associate DNA molecules and review the current knowledge on the architectural-functional organization of the eukaryotic replisome, significantly advanced by recent biochemical and structural studies. In light of this novel insight, the authors discuss the mechanisms proposed to assist interfacing of replisomes with chromatin-bound cohesin complexes and elaborate on models for nascent chromatids entrapment by cohesin in the environment of the replication fork.
黏合是在 S 期通过关键复制体因子的作用建立的,因为复制叉与黏合蛋白分子结合。通过将姐妹染色单体保持在一起,黏合对于均等分离复制的遗传物质和有效修复 DNA 断裂至关重要。然而,导致在复制过程中黏合蛋白捕获新生染色单体的分子事件才刚刚开始被理解。作者在这里描述了黏合蛋白复合物的基本结构特征及其与 DNA 分子结合的能力,并回顾了最近的生化和结构研究显著推进的真核复制体的结构-功能组织的现有知识。根据这一新的认识,作者讨论了拟议的协助复制体与染色质结合的黏合蛋白复合物相互作用的机制,并详细阐述了在复制叉环境中黏合蛋白捕获新生染色单体的模型。