RWD domain: a recurring module in kinetochore architecture shown by a Ctf19-Mcm21 complex structure

被引:52
作者
Schmitzberger, Florian [1 ]
Harrison, Stephen C. [1 ,2 ]
机构
[1] Harvard Univ, Sch Med, Dept Biol Chem & Mol Pharmacol, Boston, MA 02115 USA
[2] Harvard Univ, Sch Med, Howard Hughes Med Inst, Boston, MA 02115 USA
关键词
COMA; mitosis; X-ray crystallography; yeast; BUDDING YEAST KINETOCHORE; SACCHAROMYCES-CEREVISIAE; MOLECULAR ARCHITECTURE; OUTER KINETOCHORE; FISSION YEAST; CHROMOSOME SEGREGATION; CENP-A; PROTEIN; SPINDLE; CONSERVATION;
D O I
10.1038/embor.2012.1
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 proteins Ctf19, Okp1, Mcm21 and Ame1 are the components of COMA, a subassembly of budding-yeast kinetochores. We have determined the crystal structure of a conserved COMA subcomplex-the Ctf19-Mcm21 heterodimer-from Kluyveromyces lactis. Both proteins contain 'double-RWD' domains, which together form a Y-shaped framework with flexible N-terminal extensions. The kinetochore proteins Csm1, Spc24 and Spc25 have related single RWD domains, and Ctf19 and Mcm21 associate with pseudo-twofold symmetry analogous to that in the Csm1 homodimer and the Spc24-Spc25 heterodimer. The double-RWD domain core of the Ctf19-Mcm21 heterodimer is sufficient for association with Okp1-Ame1; the less conserved N-terminal regions may interact with components of a more extensive 'CTF19 complex'. Our structure shows the RWD domain to be a recurring module of kinetochore architecture that may be present in other kinetochore substructures. Like many eukaryotic molecular machines, kinetochores may have evolved from simpler assemblies by multiplication of a few ancestral modules.
引用
收藏
页码:216 / 222
页数:7
相关论文
共 38 条
[1]   ConSurf 2010: calculating evolutionary conservation in sequence and structure of proteins and nucleic acids [J].
Ashkenazy, Haim ;
Erez, Elana ;
Martz, Eric ;
Pupko, Tal ;
Ben-Tal, Nir .
NUCLEIC ACIDS RESEARCH, 2010, 38 :W529-W533
[2]   Structural Evidence for Common Ancestry of the Nuclear Pore Complex and Vesicle Coats [J].
Brohawn, Stephen G. ;
Leksa, Nina C. ;
Spear, Eric D. ;
Rajashankar, Kanagalaghatta R. ;
Schwartz, Thomas U. .
SCIENCE, 2008, 322 (5906) :1369-1373
[3]   Anatomy of the E2 ligase fold: Implications for enzymology and evolution of ubiquitin/Ub-like protein conjugation [J].
Burroughs, A. Maxwell ;
Jaffee, Marcie ;
Iyer, Lakshminarayan M. ;
Aravind, L. .
JOURNAL OF STRUCTURAL BIOLOGY, 2008, 162 (02) :205-218
[4]   Phospho-regulation of kinetochore-microtubule attachments by the aurora kinase Ipl1p [J].
Cheeseman, LM ;
Anderson, S ;
Jwa, M ;
Green, EM ;
Kang, JS ;
Yates, JR ;
Chan, CSM ;
Drubin, DG ;
Barnes, G .
CELL, 2002, 111 (02) :163-172
[5]   The structure of the catalytic subunit FANCL of the Fanconi anemia core complex [J].
Cole, Ambrose R. ;
Lewis, Laurence P. C. ;
Walden, Helen .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2010, 17 (03) :294-U54
[6]   The Monopolin Complex Crosslinks Kinetochore Components to Regulate Chromosome-Microtubule Attachments [J].
Corbett, Kevin D. ;
Yip, Calvin K. ;
Ee, Ly-Sha ;
Walz, Thomas ;
Amon, Angelika ;
Harrison, Stephen C. .
CELL, 2010, 142 (04) :556-567
[7]   Hierarchical assembly of the budding yeast kinetochore from multiple subcomplexes [J].
De Wulf, P ;
McAinsh, AD ;
Sorger, PK .
GENES & DEVELOPMENT, 2003, 17 (23) :2902-2921
[8]   Systematic identification of novel protein domain families associated with nuclear functions [J].
Doerks, T ;
Copley, RR ;
Schultz, J ;
Ponting, CP ;
Bork, P .
GENOME RESEARCH, 2002, 12 (01) :47-56
[9]   Establishment of Cohesion at the Pericentromere by the Ctf19 Kinetochore Subcomplex and the Replication Fork-Associated Factor, Csm3 [J].
Fernius, Josefin ;
Marston, Adele L. .
PLOS GENETICS, 2009, 5 (09)
[10]  
Fleig U, 1996, MOL CELL BIOL, V16, P6169