Structural and Functional Organization of the Ska Complex, a Key Component of the Kinetochore-Microtubule Interface

被引:130
作者
Jeyaprakash, A. Arockia [1 ,2 ]
Santamaria, Anna [3 ]
Jayachandran, Uma [1 ]
Chan, Ying Wai [3 ,4 ]
Benda, Christian [1 ]
Nigg, Erich A. [3 ]
Conti, Elena [1 ]
机构
[1] Max Planck Inst Biochem, Dept Struct Cell Biol, D-82152 Martinsried, Germany
[2] Univ Edinburgh, Inst Cell Biol, Wellcome Trust Ctr Cell Biol, Edinburgh EH9 3JR, Midlothian, Scotland
[3] Univ Basel, Biozentrum, CH-4056 Basel, Switzerland
[4] Canc Res UK, London Res Inst, Clare Hall Labs, S Mimms EN6 3LD, Herts, England
基金
瑞士国家科学基金会;
关键词
DAM1; COMPLEX; NDC80; RING COMPLEX; DEPOLYMERIZATION; ARCHITECTURE; ATTACHMENT; SPINDLE; NETWORK; POINT;
D O I
10.1016/j.molcel.2012.03.005
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 Ska complex is an essential mitotic component required for accurate cell division in human cells. It is composed of three subunits that function together to establish stable kinetochore-microtubule interactions in concert with the Ndc80 network. We show that the structure of the Ska core complex is a W-shaped dimer of coiled coils, formed by intertwined interactions between Ska1, Ska2, and Ska3. The C-terminal domains of Skal and Ska3 protrude at each end of the homodimer, bind microtubules in vitro when connected to the central core, and are essential in vivo. Mutations disrupting the central coiled coil or the dimerization interface result in chromosome congression failure followed by cell death. The Ska complex is thus endowed with bipartite and cooperative tubulin-binding properties at the ends of a 350 angstrom-long molecule. We discuss how this symmetric architecture might complement and stabilize the Ndc80-microtubule attachments with analogies to the yeast Dam1/DASH complex.
引用
收藏
页码:274 / 286
页数:13
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