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Letter
Nature Cell Biology  6, 1135 - 1141 (2004)
Published online: 24 October 2004; | doi:10.1038/ncb1187

A conserved Mis12 centromere complex is linked to heterochromatic HP1 and outer kinetochore protein Zwint-1

Chikashi Obuse1, 2, Osamu Iwasaki1, 2, Tomomi Kiyomitsu1, Gohta Goshima1, 3, Yusuke Toyoda1 & Mitsuhiro Yanagida1

1  Department of Gene Mechanisms, Graduate School of Biostudies, Kyoto University, Yoshida-Honmachi, Sakyo-ku, Kyoto 606-8501, Japan.

2  These authors contributed equally to this work.

3  Present address: Department of Cellular and Molecular Pharmacology, University of California, San Francisco, San Francisco, CA 94107, USA.

Correspondence should be addressed to Mitsuhiro Yanagida yanagida@kozo.lif.kyoto-u.ac.jp
Defects in kinetochore proteins often lead to aneuploidy and cancer. Mis12−Mtw1 is a conserved, essential kinetochore protein family. Here, we show that a Mis12 core complex exists in Schizosaccharomyces pombe and human cells. Nine polypeptides bind to human hMis12; two of these, HEC1 and Zwint-1, are authentic kinetochore proteins. Four other human proteins of unknown function (c20orf172, DC8, PMF1 and KIAA1570) correspond to yeast Mis12−Mtw1 complex components and are shown to be required for chromosome segregation in HeLa cells using RNA interference (RNAi). Surprisingly, hMis12 also forms a stable complex with the centromeric heterochromatin components HP1alpha and HP1bold gamma. Double HP1 RNAi abolishes kinetochore localization of hMis12 and DC8. Therefore, centromeric HP1 may be the base to anchor the hMis12 core complex that is enriched with coiled coils and extends to outer Zwint-1 during mitosis.


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Nature Cell Biology
ISSN: 1465-7392
EISSN: 1476-4679
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