An inner centromere protein that stimulates the microtubule depolymerizing activity of a Kinl kinesin

被引:96
作者
Ohi, R [1 ]
Coughlin, ML
Lane, WS
Mitchison, TJ
机构
[1] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[2] Harvard Univ, Harvard Microchem Facil, Cambridge, MA 02138 USA
[3] Harvard Univ, Sch Med, Inst Chem & Cell Biol, Boston, MA 02115 USA
关键词
D O I
10.1016/S1534-5807(03)00229-6
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitosis requires precise control of microtubule dynamics. The Kinl kinesin MCAK, a microtubule depolymerase, is critical for this regulation. In a screen to discover previously uncharacterized microtubule-associated proteins, we identified ICIS, a protein that stimulates MCAK activity in vitro. Consistent with this biochemical property, blocking ICIS function in Xenopus extracts with antibodies caused excessive microtubule growth and inhibited spindle formation. Prior to anaphase, ICIS localized in an MCAK-dependent manner to inner centromeres, the chromosomal region located in between sister kinetochores. From Xenopus extracts, ICIS coimmunoprecipitated MCAK and the inner centromere proteins INCENP and Aurora B, which are thought to promote chromosome biorientation. By immunoelectron microscopy, we found that ICIS is present on the surface of inner centromeres, placing it in an ideal location to depolymerize microtubules associated laterally with inner centromeres. At inner centromeres, MCAK-ICIS may destabilize these microtubules and provide a mechanism that prevents kinetochore-microtubule attachment errors.
引用
收藏
页码:309 / 321
页数:13
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