The Human Kinetochore Ska1 Complex Facilitates Microtubule Depolymerization-Coupled Motility

被引:206
|
作者
Welburn, Julie P. I. [1 ,2 ]
Grishchuk, Ekaterina L. [3 ]
Backer, Chelsea B. [1 ,2 ]
Wilson-Kubalek, Elizabeth M. [4 ]
Yates, John R., III [4 ]
Cheeseman, Iain M. [1 ,2 ]
机构
[1] MIT, Whitehead Inst Biomed Res, Cambridge, MA 02142 USA
[2] MIT, Dept Biol, Cambridge, MA 02142 USA
[3] Univ Colorado, Dept Mol Cellular & Dev Biol, Boulder, CO 80309 USA
[4] Scripps Res Inst, Dept Cell Biol, La Jolla, CA 92037 USA
关键词
MITOTIC SPINDLE; DASH COMPLEX; OUTER KINETOCHORE; NDC80; COMPLEX; FISSION YEAST; RING COMPLEX; ATTACHMENT; INTERFACE; PROTEINS; DYNAMICS;
D O I
10.1016/j.devcel.2009.01.011
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Mitotic chromosome segregation requires that kinetochores attach to microtubule polymers and harness microtubule dynamics to drive chromosome movement. In budding yeast, the Dam1 complex couples kinetochores with microtubule depolymerization. However, a metazoan homolog of the Dam1 complex has not been identified. To identify proteins that play a corresponding role at the vertebrate kinetochore-microtubule interface, we isolated a three subunit human Ska1 complex, including the previously uncharacterized protein Ramal that localizes to the outer kinetochore and spindle microtubules. Depletion of Ska1 complex subunits severely compromises proper chromosome segregation. Reconstituted Ska1 complex possesses two separable biochemical activities: direct microtubule binding through the Ska1 subunit, and microtubule-stimulated oligomenzation imparted by the Ramal subunit. The full Ska1 complex forms assemblies on microtubules that can facilitate the processive movement of microspheres along depolymerizing microtubules. In total, these results demonstrate a critical role for the Skal complex in interacting with dynamic microtubules at the outer kinetochore.
引用
收藏
页码:374 / 385
页数:12
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