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RanGTP aids anaphase entry through Ubr5-mediated protein turnover

RanGTP is known to regulate the spindle assembly checkpoint (SAC), but the underlying molecular mechanism is unclear. BuGZ stabilizes SAC protein Bub3 through direct interaction and facilitates its mitotic function. Here we show that RanGTP promotes the turnover of BuGZ and Bub3 in metaphase, which...

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Detalles Bibliográficos
Autores principales: Jiang, Hao, He, Xiaonan, Feng, Di, Zhu, Xueliang, Zheng, Yixian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Rockefeller University Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602037/
https://www.ncbi.nlm.nih.gov/pubmed/26438829
http://dx.doi.org/10.1083/jcb.201503122
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author Jiang, Hao
He, Xiaonan
Feng, Di
Zhu, Xueliang
Zheng, Yixian
author_facet Jiang, Hao
He, Xiaonan
Feng, Di
Zhu, Xueliang
Zheng, Yixian
author_sort Jiang, Hao
collection PubMed
description RanGTP is known to regulate the spindle assembly checkpoint (SAC), but the underlying molecular mechanism is unclear. BuGZ stabilizes SAC protein Bub3 through direct interaction and facilitates its mitotic function. Here we show that RanGTP promotes the turnover of BuGZ and Bub3 in metaphase, which in turn facilitates metaphase-to-anaphase transition. BuGZ and Bub3 interact with either importin-β or an E3 ubiquitin ligase, Ubr5. RanGTP promotes the dissociation of importin-β from BuGZ and Bub3 in metaphase. This results in increased binding of BuGZ and Bub3 to Ubr5, leading to ubiquitination and subsequent turnover of both proteins. We propose that elevated metaphase RanGTP levels use Ubr5 to couple overall chromosome congression to SAC silencing.
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spelling pubmed-46020372016-04-12 RanGTP aids anaphase entry through Ubr5-mediated protein turnover Jiang, Hao He, Xiaonan Feng, Di Zhu, Xueliang Zheng, Yixian J Cell Biol Research Articles RanGTP is known to regulate the spindle assembly checkpoint (SAC), but the underlying molecular mechanism is unclear. BuGZ stabilizes SAC protein Bub3 through direct interaction and facilitates its mitotic function. Here we show that RanGTP promotes the turnover of BuGZ and Bub3 in metaphase, which in turn facilitates metaphase-to-anaphase transition. BuGZ and Bub3 interact with either importin-β or an E3 ubiquitin ligase, Ubr5. RanGTP promotes the dissociation of importin-β from BuGZ and Bub3 in metaphase. This results in increased binding of BuGZ and Bub3 to Ubr5, leading to ubiquitination and subsequent turnover of both proteins. We propose that elevated metaphase RanGTP levels use Ubr5 to couple overall chromosome congression to SAC silencing. The Rockefeller University Press 2015-10-12 /pmc/articles/PMC4602037/ /pubmed/26438829 http://dx.doi.org/10.1083/jcb.201503122 Text en © 2015 Jiang 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.rupress.org/terms). 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
Jiang, Hao
He, Xiaonan
Feng, Di
Zhu, Xueliang
Zheng, Yixian
RanGTP aids anaphase entry through Ubr5-mediated protein turnover
title RanGTP aids anaphase entry through Ubr5-mediated protein turnover
title_full RanGTP aids anaphase entry through Ubr5-mediated protein turnover
title_fullStr RanGTP aids anaphase entry through Ubr5-mediated protein turnover
title_full_unstemmed RanGTP aids anaphase entry through Ubr5-mediated protein turnover
title_short RanGTP aids anaphase entry through Ubr5-mediated protein turnover
title_sort rangtp aids anaphase entry through ubr5-mediated protein turnover
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4602037/
https://www.ncbi.nlm.nih.gov/pubmed/26438829
http://dx.doi.org/10.1083/jcb.201503122
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