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姐妹染色单体配对的机制。

Mechanisms of sister chromatid pairing.

作者信息

Skibbens Robert V

机构信息

Department of Biological Sciences, Lehigh University, Bethlehem, Pennsylvania 18015, USA.

出版信息

Int Rev Cell Mol Biol. 2008;269:283-339. doi: 10.1016/S1937-6448(08)01005-8.

Abstract

The continuance of life through cell division requires high fidelity DNA replication and chromosome segregation. During DNA replication, each parental chromosome is duplicated exactly and one time only. At the same time, the resulting chromosomes (called sister chromatids) become tightly paired along their length. This S-phase pairing, or cohesion, identifies chromatids as sisters over time. During mitosis in most eukaryotes, sister chromatids bi-orient to the mitotic spindle. After each chromosome pair is properly oriented, the cohesion established during S phase is inactivated in a tightly regulated fashion, allowing sister chromatids to segregate away from each other. Recent findings of cohesin structure and enzymology provide new insights into cohesion, while many critical facets of cohesion (how cohesins tether together sister chromatids and how those tethers are established) remain actively debated.

摘要

通过细胞分裂维持生命需要高保真的DNA复制和染色体分离。在DNA复制过程中,每条亲代染色体被精确复制且仅复制一次。同时,产生的染色体(称为姐妹染色单体)沿其长度紧密配对。这种S期配对或黏连随着时间推移将染色单体识别为姐妹染色单体。在大多数真核生物的有丝分裂过程中,姐妹染色单体双定向于有丝分裂纺锤体。在每对染色体正确定向后,S期建立的黏连以严格调控的方式失活,使姐妹染色单体彼此分离。黏连蛋白结构和酶学的最新发现为黏连提供了新见解,而黏连的许多关键方面(黏连蛋白如何将姐妹染色单体拴在一起以及这些连接是如何建立的)仍在激烈争论中。

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