Nasmyth Kim, Haering Christian H
Institute of Molecular Pathology, A-1030 Vienna, Austria.
Annu Rev Biochem. 2005;74:595-648. doi: 10.1146/annurev.biochem.74.082803.133219.
Protein complexes consisting of structural maintenance of chromosomes (SMC) and kleisin subunits are crucial for the faithful segregation of chromosomes during cell proliferation in prokaryotes and eukaryotes. Two of the best-studied SMC complexes are cohesin and condensin. Cohesin is required to hold sister chromatids together, which allows their bio-orientation on the mitotic spindle. Cleavage of cohesin's kleisin subunit by the separase protease then triggers the movement of sister chromatids into opposite halves of the cell during anaphase. Condensin is required to organize mitotic chromosomes into coherent structures that prevent them from getting tangled up during segregation. Here we describe the discovery of SMC complexes and discuss recent advances in determining how members of this ancient protein family may function at a mechanistic level.
由染色体结构维持(SMC)和kleisin亚基组成的蛋白质复合物对于原核生物和真核生物细胞增殖过程中染色体的准确分离至关重要。研究得最为透彻的两种SMC复合物是黏连蛋白和凝缩蛋白。黏连蛋白需要将姐妹染色单体结合在一起,这使得它们能够在有丝分裂纺锤体上进行生物定向。然后,分离酶蛋白酶切割黏连蛋白的kleisin亚基,从而在后期触发姐妹染色单体向细胞的相反两极移动。凝缩蛋白需要将有丝分裂染色体组织成连贯的结构,以防止它们在分离过程中缠结在一起。在这里,我们描述了SMC复合物的发现,并讨论了在确定这个古老蛋白质家族的成员如何在分子机制层面发挥作用方面的最新进展。