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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...

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Autores principales: Rattani, Ahmed, Wolna, Magda, Ploquin, Mickael, Helmhart, Wolfgang, Morrone, Seamus, Mayer, Bernd, Godwin, Jonathan, Xu, Wenqing, Stemmann, Olaf, Pendas, Alberto, Nasmyth, Kim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2013
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
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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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