共 57 条
Linking kinetochore-microtubule binding to the spindle checkpoint
被引:58
作者:

Burke, Daniel J.
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Virginia, Med Ctr, Dept Biochem & Mol Genet, Charlottesville, VA 22908 USA Univ Virginia, Med Ctr, Dept Biochem & Mol Genet, Charlottesville, VA 22908 USA

Stukenberg, P. Todd
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h-index: 0
机构:
Univ Virginia, Med Ctr, Dept Biochem & Mol Genet, Charlottesville, VA 22908 USA Univ Virginia, Med Ctr, Dept Biochem & Mol Genet, Charlottesville, VA 22908 USA
机构:
[1] Univ Virginia, Med Ctr, Dept Biochem & Mol Genet, Charlottesville, VA 22908 USA
关键词:
D O I:
10.1016/j.devcel.2008.03.015
中图分类号:
Q2 [细胞生物学];
学科分类号:
071009 ;
090102 ;
摘要:
The spindle checkpoint blocks cell-cycle progression until chromosomes are properly attached to the mitotic spindle. Popular models propose that checkpoint proteins associate with kinetochores to produce a "wait anaphase" signal that inhibits anaphase. Recent data suggest that a two-state switch results from using the same kinetochore proteins to bind microtubules and checkpoint proteins. At least eight protein kinases are implicated in spindle checkpoint signaling, arguing that a traditional signal transduction cascade is integral to spindle checkpoint signaling.
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页码:474 / 479
页数:6
相关论文
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