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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Rockefeller University Press
2015
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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. |
format | Online Article Text |
id | pubmed-4602037 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | The Rockefeller University Press |
record_format | MEDLINE/PubMed |
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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