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Published online
doi:10.1083/jcb.200801049
The Journal of Cell Biology, Vol. 183, No. 2, 267-277
The Rockefeller University Press, 0021-9525 $30.00
© Osmundson et al.
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Article

The HECT E3 ligase Smurf2 is required for Mad2-dependent spindle assembly checkpoint



Evan C. Osmundson1,3, Dipankar Ray1, Finola E. Moore1, Qingshen Gao2,4, Gerald H. Thomsen5,6, and Hiroaki Kiyokawa1,2,3

1 Department of Molecular Pharmacology and Biological Chemistry and 2 Robert H. Lurie Comprehensive Cancer Center, Feinberg School of Medicine, Northwestern University, Chicago, IL 60611
3 Department of Biochemistry and Molecular Genetics, College of Medicine, University of Illinois, Chicago, IL 60607
4 Department of Medicine, Evanston Northwestern Healthcare Research Institute, Evanston, IL 60201
5 Department of Biochemistry and Cell Biology and 6 Center for Developmental Genetics, Stony Brook University, Stony Brook, NY 11794

Correspondence to Hiroaki Kiyokawa: Kiyokawa{at}northwestern.edu

Activation of the anaphase-promoting complex/cyclosome (APC/C) by Cdc20 is critical for the metaphase–anaphase transition. APC/C-Cdc20 is required for polyubiquitination and degradation of securin and cyclin B at anaphase onset. The spindle assembly checkpoint delays APC/C-Cdc20 activation until all kinetochores attach to mitotic spindles. In this study, we demonstrate that a HECT (homologous to the E6-AP carboxyl terminus) ubiquitin ligase, Smurf2, is required for the spindle checkpoint. Smurf2 localizes to the centrosome, mitotic midbody, and centromeres. Smurf2 depletion or the expression of a catalytically inactive Smurf2 results in misaligned and lagging chromosomes, premature anaphase onset, and defective cytokinesis. Smurf2 inactivation prevents nocodazole-treated cells from accumulating cyclin B and securin and prometaphase arrest. The silencing of Cdc20 in Smurf2-depleted cells restores mitotic accumulation of cyclin B and securin. Smurf2 depletion results in enhanced polyubiquitination and degradation of Mad2, a critical checkpoint effector. Mad2 is mislocalized in Smurf2-depleted cells, suggesting that Smurf2 regulates the localization and stability of Mad2. These data indicate that Smurf2 is a novel mitotic regulator.

Abbreviations used in this paper: ACA, anticentromere antibody; APC/C, anaphase-promoting complex/cyclosome; dsRNA, double-stranded RNA; HECT, homologous to the E6-AP carboxyl terminus; MCC, mitotic checkpoint complex.

© 2008 Osmundson et al. This article is distributed under the terms of an Attribution–Noncommercial–Share Alike–No Mirror Sites license for the first six months after the publication date (see http://www.jcb.org/misc/terms.shtml). After six months it is available under a Creative Commons License (Attribution–Noncommercial–Share Alike 3.0 Unported license, as described at http://creativecommons.org/licenses/by-nc-sa/3.0/).


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