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Sgol2 provides a regulatory platform that coordinates essential cell cycle processes during meiosis I in oocytes
Accurate chromosome segregation depends on coordination between cohesion resolution and kinetochore-microtubule interactions (K-fibers), a process regulated by the spindle assembly checkpoint (SAC). How these diverse processes are coordinated remains unclear. We show that in mammalian oocytes Shugos...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3816256/ https://www.ncbi.nlm.nih.gov/pubmed/24192037 http://dx.doi.org/10.7554/eLife.01133 |
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author | Rattani, Ahmed Wolna, Magda Ploquin, Mickael Helmhart, Wolfgang Morrone, Seamus Mayer, Bernd Godwin, Jonathan Xu, Wenqing Stemmann, Olaf Pendas, Alberto Nasmyth, Kim |
author_facet | Rattani, Ahmed Wolna, Magda Ploquin, Mickael Helmhart, Wolfgang Morrone, Seamus Mayer, Bernd Godwin, Jonathan Xu, Wenqing Stemmann, Olaf Pendas, Alberto Nasmyth, Kim |
author_sort | Rattani, Ahmed |
collection | PubMed |
description | Accurate chromosome segregation depends on coordination between cohesion resolution and kinetochore-microtubule interactions (K-fibers), a process regulated by the spindle assembly checkpoint (SAC). How these diverse processes are coordinated remains unclear. We show that in mammalian oocytes Shugoshin-like protein 2 (Sgol2) in addition to protecting cohesin, plays an important role in turning off the SAC, in promoting the congression and bi-orientation of bivalents on meiosis I spindles, in facilitating formation of K-fibers and in limiting bivalent stretching. Sgol2’s ability to protect cohesin depends on its interaction with PP2A, as is its ability to silence the SAC, with the latter being mediated by direct binding to Mad2. In contrast, its effect on bivalent stretching and K-fiber formation is independent of PP2A and mediated by recruitment of MCAK and inhibition of Aurora C kinase activity respectively. By virtue of its multiple interactions, Sgol2 links many of the processes essential for faithful chromosome segregation. DOI: http://dx.doi.org/10.7554/eLife.01133.001 |
format | Online Article Text |
id | pubmed-3816256 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-38162562013-11-06 Sgol2 provides a regulatory platform that coordinates essential cell cycle processes during meiosis I in oocytes Rattani, Ahmed Wolna, Magda Ploquin, Mickael Helmhart, Wolfgang Morrone, Seamus Mayer, Bernd Godwin, Jonathan Xu, Wenqing Stemmann, Olaf Pendas, Alberto Nasmyth, Kim eLife Cell Biology Accurate chromosome segregation depends on coordination between cohesion resolution and kinetochore-microtubule interactions (K-fibers), a process regulated by the spindle assembly checkpoint (SAC). How these diverse processes are coordinated remains unclear. We show that in mammalian oocytes Shugoshin-like protein 2 (Sgol2) in addition to protecting cohesin, plays an important role in turning off the SAC, in promoting the congression and bi-orientation of bivalents on meiosis I spindles, in facilitating formation of K-fibers and in limiting bivalent stretching. Sgol2’s ability to protect cohesin depends on its interaction with PP2A, as is its ability to silence the SAC, with the latter being mediated by direct binding to Mad2. In contrast, its effect on bivalent stretching and K-fiber formation is independent of PP2A and mediated by recruitment of MCAK and inhibition of Aurora C kinase activity respectively. By virtue of its multiple interactions, Sgol2 links many of the processes essential for faithful chromosome segregation. DOI: http://dx.doi.org/10.7554/eLife.01133.001 eLife Sciences Publications, Ltd 2013-11-05 /pmc/articles/PMC3816256/ /pubmed/24192037 http://dx.doi.org/10.7554/eLife.01133 Text en Copyright © 2013, Rattani et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Cell Biology Rattani, Ahmed Wolna, Magda Ploquin, Mickael Helmhart, Wolfgang Morrone, Seamus Mayer, Bernd Godwin, Jonathan Xu, Wenqing Stemmann, Olaf Pendas, Alberto Nasmyth, Kim Sgol2 provides a regulatory platform that coordinates essential cell cycle processes during meiosis I in oocytes |
title | Sgol2 provides a regulatory platform that coordinates essential cell cycle processes during meiosis I in oocytes |
title_full | Sgol2 provides a regulatory platform that coordinates essential cell cycle processes during meiosis I in oocytes |
title_fullStr | Sgol2 provides a regulatory platform that coordinates essential cell cycle processes during meiosis I in oocytes |
title_full_unstemmed | Sgol2 provides a regulatory platform that coordinates essential cell cycle processes during meiosis I in oocytes |
title_short | Sgol2 provides a regulatory platform that coordinates essential cell cycle processes during meiosis I in oocytes |
title_sort | sgol2 provides a regulatory platform that coordinates essential cell cycle processes during meiosis i in oocytes |
topic | Cell Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3816256/ https://www.ncbi.nlm.nih.gov/pubmed/24192037 http://dx.doi.org/10.7554/eLife.01133 |
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