Reconstituting the kinetochore-microtubule interface: what, why, and how

被引:14
作者
Akiyoshi, Bungo [1 ]
Biggins, Sue [2 ]
机构
[1] Univ Oxford, Sir William Dunn Sch Pathol, Oxford OX1 3RE, England
[2] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98109 USA
基金
美国国家卫生研究院;
关键词
SPINDLE-ASSEMBLY CHECKPOINT; AURORA-B KINASE; PROTEIN PHOSPHATASE 1; CENP-A NUCLEOSOMES; BUDDING YEAST; MITOTIC SPINDLE; FISSION YEAST; DAM1; COMPLEX; MOLECULAR ARCHITECTURE; OUTER KINETOCHORE;
D O I
10.1007/s00412-012-0362-0
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The kinetochore is the proteinaceous complex that governs the movement of duplicated chromosomes by interacting with spindle microtubules during mitosis and meiosis. Faithful chromosome segregation requires that kinetochores form robust load-bearing attachments to the tips of dynamic spindle microtubules, correct microtubule attachment errors, and delay the onset of anaphase until all chromosomes have made proper attachments. To understand how this macromolecular machine operates to segregate duplicated chromosomes with exquisite accuracy, it is critical to reconstitute and study kinetochore-microtubule interactions in vitro using defined components. Here, we review the current status of reconstitution as well as recent progress in understanding the microtubule-binding functions of kinetochores in vivo.
引用
收藏
页码:235 / 250
页数:16
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