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

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...

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Autores principales: Osmundson, Evan C., Ray, Dipankar, Moore, Finola E., Gao, Qingshen, Thomsen, Gerald H., Kiyokawa, Hiroaki
Formato: Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2568023/
https://www.ncbi.nlm.nih.gov/pubmed/18852296
http://dx.doi.org/10.1083/jcb.200801049
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author Osmundson, Evan C.
Ray, Dipankar
Moore, Finola E.
Gao, Qingshen
Thomsen, Gerald H.
Kiyokawa, Hiroaki
author_facet Osmundson, Evan C.
Ray, Dipankar
Moore, Finola E.
Gao, Qingshen
Thomsen, Gerald H.
Kiyokawa, Hiroaki
author_sort Osmundson, Evan C.
collection PubMed
description 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.
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spelling pubmed-25680232009-04-20 The HECT E3 ligase Smurf2 is required for Mad2-dependent spindle assembly checkpoint Osmundson, Evan C. Ray, Dipankar Moore, Finola E. Gao, Qingshen Thomsen, Gerald H. Kiyokawa, Hiroaki J Cell Biol Research Articles 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. The Rockefeller University Press 2008-10-20 /pmc/articles/PMC2568023/ /pubmed/18852296 http://dx.doi.org/10.1083/jcb.200801049 Text en © 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/).
spellingShingle Research Articles
Osmundson, Evan C.
Ray, Dipankar
Moore, Finola E.
Gao, Qingshen
Thomsen, Gerald H.
Kiyokawa, Hiroaki
The HECT E3 ligase Smurf2 is required for Mad2-dependent spindle assembly checkpoint
title The HECT E3 ligase Smurf2 is required for Mad2-dependent spindle assembly checkpoint
title_full The HECT E3 ligase Smurf2 is required for Mad2-dependent spindle assembly checkpoint
title_fullStr The HECT E3 ligase Smurf2 is required for Mad2-dependent spindle assembly checkpoint
title_full_unstemmed The HECT E3 ligase Smurf2 is required for Mad2-dependent spindle assembly checkpoint
title_short The HECT E3 ligase Smurf2 is required for Mad2-dependent spindle assembly checkpoint
title_sort hect e3 ligase smurf2 is required for mad2-dependent spindle assembly checkpoint
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2568023/
https://www.ncbi.nlm.nih.gov/pubmed/18852296
http://dx.doi.org/10.1083/jcb.200801049
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