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Mps1 kinase promotes sister-kinetochore bi-orientation by a tension-dependent mechanism
被引:91
作者:
Maure, Jean-Frangois
[1
]
Kitamura, Etsushi
[1
]
Tanaka, Tomoyuki U.
[1
]
机构:
[1] Univ Dundee, Coll Life Sci, Wellcome Trust Ctr Gene Regulat & Express, Dundee DD1 5EH, Scotland
关键词:
D O I:
10.1016/j.cub.2007.11.032
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:
Segregation of sister chromatids to opposite spindle poles during anaphase is dependent on the prior capture of sister kinetochores by microtubules extending from opposite spindle poles (bi-orientation). If sister kinetochores attach to microtubules from the same pole (syntelic attachment), the kinetochore-spindle pole connections must be re-oriented to be converted to proper bi-orientation [1, 2]. This re-orientation is facilitated by Aurora B kinase (IpI1 in budding yeast), which eliminates kinetochore-spindle pole connections that do not generate tension [3-6]. Mps1 is another evolutionarily conserved protein kinase, required for spindle-assembly checkpoint and, in some organisms, for duplication of microtubule-organizing centers [7]. Separately from these functions, however, Mps1 has an important role in chromosome segregation [8]. Here we show that, in budding yeast, Mps1 has a crucial role in establishing sister-kinetochore bi-orientation on the mitotic spindle. Failure in bi-orientation with inactive Mps1 is not due to a lack of kinetochore-spindle pole connections by microtubules, but due to a defect in properly orienting the connections. Mps1 promotes re-orientation of kinetochore-spindle pole connections and eliminates those that do not generate tension between sister kinetochores. We did not find evidence that IpI1 regulates Mps1 or vice versa; therefore, they play similar, but possibly independent, roles in facilitating bi-orientation.
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页码:2175 / 2182
页数:8
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