Kinetochore microtubule dynamics and attachment stability are regulated by Hec1

被引:585
作者
DeLuca, Jennifer G.
Gall, Walter E.
Ciferri, Claudio
Cimini, Daniela
Musacchio, Andrea
Salmon, E. D.
机构
[1] Univ N Carolina, Dept Biol, Chapel Hill, NC 27599 USA
[2] Virginia Polytech Inst & State Univ, Dept Biol Sci, Blacksburg, VA 24061 USA
[3] European Inst Oncol, Dept Expt Oncol, I-20141 Milan, Italy
关键词
D O I
10.1016/j.cell.2006.09.047
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
Mitotic cells face the challenging tasks of linking kinetochores to growing and, shortening microtubules and actively regulating these dynamic attachments to produce accurate chromosome segregation. We report here that Ndc80/Hec1 functions in regulating kinetochore microtubule plus-end dynamics and attachment stability. Microinjection of an antibody to the N terminus of Hec1 suppresses both microtubule detachment and microtubule plus-end polymerization and depolymerization at kinetochores of PtK1 cells. Centromeres become hyperstretched, kinetochore fibers shorten from spindle poles, kinetochore microtubule attachment errors increase, and chromosomes severely mis-segregate. The N terminus of Hec1 is phosphorylated by Aurora B kinase in vitro, and cells expressing N-terminal nonphosphorylatable mutants of Hec1 exhibit an increase in merotelic attachments, hyperstretching of centromeres, and errors in chromosome segregation. These findings reveal a key role for the Hec1 N terminus in controlling dynamic behavior of kinetochore microtubules.
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收藏
页码:969 / 982
页数:14
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