Architecture of the human Ndc80-Hec1 complex, a critical constituent of the outer kinetochore

被引:143
作者
Ciferri, C
De Luca, J
Monzani, S
Ferrari, KJ
Ristic, D
Wyman, C
Stark, H
Kilmartin, J
Salmon, ED
Musacchio, A
机构
[1] European Inst Oncol, Dept Expt Oncol, I-20141 Milan, Italy
[2] Inst Mol Oncol Fdn, Italian Fdn Canc Res FIRC, I-20139 Milan, Italy
[3] Univ N Carolina, Dept Biol, Chapel Hill, NC 27599 USA
[4] Dr Daniel Den Hoed Canc Ctr, Dept Radiat Oncol, NL-3000 DR Rotterdam, Netherlands
[5] Erasmus Univ, Ctr Med, Dept Cell Biol & Genet, NL-3000 DR Rotterdam, Netherlands
[6] Max Planck Inst Biophys Chem, D-37077 Gottingen, Germany
[7] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
关键词
D O I
10.1074/jbc.M504070200
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
The Ndc80 complex is a constituent of the outer plate of the kinetochore and plays a critical role in establishing the stable kinetochore-microtubule interactions required for chromosome segregation in mitosis. The Ndc80 complex is evolutionarily conserved and contains the four subunits Spc24, Spc25, Nuf2, and Ndc80 ( whose human homologue is called Hec1). All four subunits are predicted to contain globular domains and extensive coiled coil regions. To gain an insight into the organization of the human Ndc80 complex, we reconstituted it using recombinant methods. The hydrodynamic properties of the recombinant Ndc80 complex are identical to those of the endogenous HeLa cell complex and are consistent with a 1: 1: 1: 1 stoichiometry of the four subunits and a very elongated shape. Two tight Hec1-Nuf2 and Spc24-Spc25 subcomplexes, each stabilized by a parallel heterodimeric coiled coil, maintain this organization. These subcomplexes tetramerize via an interaction of the C- and N-terminal portions of the Hec1-Nuf2 and Spc24-Spc25 coiled coils, respectively. The recombinant complex displays normal kinetochore localization upon injection in HeLa cells and is therefore a faithful copy of the endogenous Ndc80 complex.
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页码:29088 / 29095
页数:8
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