Uhlmann Frank
Lincoln's Inn Fields Laboratories, Cancer Research UK, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.
Curr Biol. 2003 Feb 4;13(3):R104-14. doi: 10.1016/s0960-9822(03)00039-3.
Sister chromatid cohesion and separation are fundamental for accurate genome inheritance over cell generations. Work over recent years has established the existence of a chromosomal protein complex, cohesin, that connects sister chromatids from the time they are generated in S phase onwards, and which is destroyed at the onset of anaphase through cleavage by the protease separase. Over the last year, the function of cohesin has been investigated in higher eukaryotes, including humans, with results that have uncovered important new aspects of this process. The first structural views of cohesin have become available, and significant steps been made towards a mechanistic understanding of chromosome cohesion. Studies on separase have revealed new levels of regulation of chromosome segregation.
姐妹染色单体的黏连与分离对于基因组在细胞世代间的准确遗传至关重要。近年来的研究证实了一种染色体蛋白复合体——黏连蛋白的存在,它从姐妹染色单体在S期生成之时起就将它们连接在一起,并在后期开始时被蛋白酶分离酶切割而破坏。在过去的一年里,人们对包括人类在内的高等真核生物中黏连蛋白的功能进行了研究,结果揭示了这一过程重要的新方面。黏连蛋白的首批结构视图已经可得,并且在对染色体黏连的机制理解方面取得了重大进展。对分离酶的研究揭示了染色体分离调控的新层面。