The molecular basis of sister-chromatid cohesion

被引:140
作者
Lee, JY [1 ]
Orr-Weaver, TL
机构
[1] MIT, Whitehead Inst, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA 02142 USA
关键词
chromosome segregation; meiosis; mitosis; kinetochore; chiasmata;
D O I
10.1146/annurev.cellbio.17.1.753
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The replicated copies of each chromosome, the sister chromatids, are attached prior to their segregation in mitosis and meiosis. This association or cohesion is critical for each sister chromatid to bind to microtubules from opposite spindle poles and thus segregate away from each other at anaphase of mitosis or meiosis II. The cohesin protein complex is essential for cohesion in both mitosis and meiosis, and cleavage of one of the subunits is sufficient for loss of cohesion at anaphase. The localization of the cohesin complex and other cohesion proteins permits evaluation of the positions of sister-chromatid associations within the chromosome structure, as well as the relationship between cohesion and condensation. Recently, two key riddles in the mechanism of meiotic chromosome segregation have yielded to molecular answers. First, analysis of the cohesin complex in meiosis provides molecular support for the long-standing hypothesis that sister-chromatid cohesion links homologs in meiosis I by stabilizing chiasmata. Second, the isolation of the monopolin protein that controls kinetochore behavior in meiosis I defines a functional basis by which sister kinetochores are directed toward the same pole in meiosis I.
引用
收藏
页码:753 / 777
页数:29
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