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PTEN regulates spindle assembly checkpoint timing through MAD1 in interphase

The spindle assembly checkpoint (SAC) restrains anaphase progression to ensure all chromosomes attach properly to the spindle. Although SAC timing has been extensively investigated in mitosis, its mechanism of regulation in interphase is unclear. We report that PTEN functions as a crucial activator...

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Detalles Bibliográficos
Autores principales: Liu, Yu, Du, Xiao, Zhang, Shuting, Liu, Yang, Zhang, Qiaoling, Yin, Qi, McNutt, Michael A., Yin, Yuxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716712/
https://www.ncbi.nlm.nih.gov/pubmed/29228672
http://dx.doi.org/10.18632/oncotarget.20532
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author Liu, Yu
Du, Xiao
Zhang, Shuting
Liu, Yang
Zhang, Qiaoling
Yin, Qi
McNutt, Michael A.
Yin, Yuxin
author_facet Liu, Yu
Du, Xiao
Zhang, Shuting
Liu, Yang
Zhang, Qiaoling
Yin, Qi
McNutt, Michael A.
Yin, Yuxin
author_sort Liu, Yu
collection PubMed
description The spindle assembly checkpoint (SAC) restrains anaphase progression to ensure all chromosomes attach properly to the spindle. Although SAC timing has been extensively investigated in mitosis, its mechanism of regulation in interphase is unclear. We report that PTEN functions as a crucial activator of SAC timing and protects chromosome segregation under both spindle poison treated and untreated conditions. We show that PTEN physically interacts with MAD1 and promotes its dimerization and localization in the nuclear pore. Consequently, PTEN is important for the formation of the mitotic checkpoint complex (MCC) in interphase. We propose PTEN/MAD1 signaling is essential for maintenance of SAC timing and chromosome integrity.
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spelling pubmed-57167122017-12-08 PTEN regulates spindle assembly checkpoint timing through MAD1 in interphase Liu, Yu Du, Xiao Zhang, Shuting Liu, Yang Zhang, Qiaoling Yin, Qi McNutt, Michael A. Yin, Yuxin Oncotarget Research Paper The spindle assembly checkpoint (SAC) restrains anaphase progression to ensure all chromosomes attach properly to the spindle. Although SAC timing has been extensively investigated in mitosis, its mechanism of regulation in interphase is unclear. We report that PTEN functions as a crucial activator of SAC timing and protects chromosome segregation under both spindle poison treated and untreated conditions. We show that PTEN physically interacts with MAD1 and promotes its dimerization and localization in the nuclear pore. Consequently, PTEN is important for the formation of the mitotic checkpoint complex (MCC) in interphase. We propose PTEN/MAD1 signaling is essential for maintenance of SAC timing and chromosome integrity. Impact Journals LLC 2017-08-24 /pmc/articles/PMC5716712/ /pubmed/29228672 http://dx.doi.org/10.18632/oncotarget.20532 Text en Copyright: © 2017 Liu 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/) (CC-BY), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Research Paper
Liu, Yu
Du, Xiao
Zhang, Shuting
Liu, Yang
Zhang, Qiaoling
Yin, Qi
McNutt, Michael A.
Yin, Yuxin
PTEN regulates spindle assembly checkpoint timing through MAD1 in interphase
title PTEN regulates spindle assembly checkpoint timing through MAD1 in interphase
title_full PTEN regulates spindle assembly checkpoint timing through MAD1 in interphase
title_fullStr PTEN regulates spindle assembly checkpoint timing through MAD1 in interphase
title_full_unstemmed PTEN regulates spindle assembly checkpoint timing through MAD1 in interphase
title_short PTEN regulates spindle assembly checkpoint timing through MAD1 in interphase
title_sort pten regulates spindle assembly checkpoint timing through mad1 in interphase
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5716712/
https://www.ncbi.nlm.nih.gov/pubmed/29228672
http://dx.doi.org/10.18632/oncotarget.20532
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