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Dual mechanisms regulate the recruitment of spindle assembly checkpoint proteins to the budding yeast kinetochore

Recruitment of spindle assembly checkpoint (SAC) proteins by an unattached kinetochore leads to SAC activation. This recruitment is licensed by the Mps1 kinase, which phosphorylates the kinetochore protein Spc105 at one or more of its six MELT repeats. Spc105 then recruits the Bub3-Bub1 and Mad1-Mad...

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Autores principales: Aravamudhan, Pavithra, Chen, Renjie, Roy, Babhrubahan, Sim, Janice, Joglekar, Ajit P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5221577/
https://www.ncbi.nlm.nih.gov/pubmed/27170178
http://dx.doi.org/10.1091/mbc.E16-01-0007
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author Aravamudhan, Pavithra
Chen, Renjie
Roy, Babhrubahan
Sim, Janice
Joglekar, Ajit P.
author_facet Aravamudhan, Pavithra
Chen, Renjie
Roy, Babhrubahan
Sim, Janice
Joglekar, Ajit P.
author_sort Aravamudhan, Pavithra
collection PubMed
description Recruitment of spindle assembly checkpoint (SAC) proteins by an unattached kinetochore leads to SAC activation. This recruitment is licensed by the Mps1 kinase, which phosphorylates the kinetochore protein Spc105 at one or more of its six MELT repeats. Spc105 then recruits the Bub3-Bub1 and Mad1-Mad2 complexes, which produce the inhibitory signal that arrests cell division. The strength of this signal depends, in part, on the number of Bub3-Bub1 and Mad1-Mad2 molecules that Spc105 recruits. Therefore regulation of this recruitment will influence SAC signaling. To understand this regulation, we established the physiological binding curves that describe the binding of Bub3-Bub1 and Mad1-Mad2 to the budding yeast kinetochore. We find that the binding of both follows the mass action law. Mps1 likely phosphorylates all six MELT repeats of Spc105. However, two mechanisms prevent Spc105 from recruiting six Bub3-Bub1 molecules: low Bub1 abundance and hindrance in the binding of more than one Bub3-Bub1 molecule to the same Spc105. Surprisingly, the kinetochore recruits two Mad1-Mad2 heterotetramers for every Bub3-Bub1 molecule. Finally, at least three MELT repeats per Spc105 are needed for accurate chromosome segregation. These data reveal that kinetochore-intrinsic and -extrinsic mechanisms influence the physiological operation of SAC signaling, potentially to maximize chromosome segregation accuracy.
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spelling pubmed-52215772017-01-22 Dual mechanisms regulate the recruitment of spindle assembly checkpoint proteins to the budding yeast kinetochore Aravamudhan, Pavithra Chen, Renjie Roy, Babhrubahan Sim, Janice Joglekar, Ajit P. Mol Biol Cell Articles Recruitment of spindle assembly checkpoint (SAC) proteins by an unattached kinetochore leads to SAC activation. This recruitment is licensed by the Mps1 kinase, which phosphorylates the kinetochore protein Spc105 at one or more of its six MELT repeats. Spc105 then recruits the Bub3-Bub1 and Mad1-Mad2 complexes, which produce the inhibitory signal that arrests cell division. The strength of this signal depends, in part, on the number of Bub3-Bub1 and Mad1-Mad2 molecules that Spc105 recruits. Therefore regulation of this recruitment will influence SAC signaling. To understand this regulation, we established the physiological binding curves that describe the binding of Bub3-Bub1 and Mad1-Mad2 to the budding yeast kinetochore. We find that the binding of both follows the mass action law. Mps1 likely phosphorylates all six MELT repeats of Spc105. However, two mechanisms prevent Spc105 from recruiting six Bub3-Bub1 molecules: low Bub1 abundance and hindrance in the binding of more than one Bub3-Bub1 molecule to the same Spc105. Surprisingly, the kinetochore recruits two Mad1-Mad2 heterotetramers for every Bub3-Bub1 molecule. Finally, at least three MELT repeats per Spc105 are needed for accurate chromosome segregation. These data reveal that kinetochore-intrinsic and -extrinsic mechanisms influence the physiological operation of SAC signaling, potentially to maximize chromosome segregation accuracy. The American Society for Cell Biology 2016-11-07 /pmc/articles/PMC5221577/ /pubmed/27170178 http://dx.doi.org/10.1091/mbc.E16-01-0007 Text en © 2016 Aravamudhan et al. This article is distributed by The American Society for Cell Biology under license from the author(s). Two months after publication it is available to the public under an Attribution–Noncommercial–Share Alike 3.0 Unported Creative Commons License (http://creativecommons.org/licenses/by-nc-sa/3.0). “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology.
spellingShingle Articles
Aravamudhan, Pavithra
Chen, Renjie
Roy, Babhrubahan
Sim, Janice
Joglekar, Ajit P.
Dual mechanisms regulate the recruitment of spindle assembly checkpoint proteins to the budding yeast kinetochore
title Dual mechanisms regulate the recruitment of spindle assembly checkpoint proteins to the budding yeast kinetochore
title_full Dual mechanisms regulate the recruitment of spindle assembly checkpoint proteins to the budding yeast kinetochore
title_fullStr Dual mechanisms regulate the recruitment of spindle assembly checkpoint proteins to the budding yeast kinetochore
title_full_unstemmed Dual mechanisms regulate the recruitment of spindle assembly checkpoint proteins to the budding yeast kinetochore
title_short Dual mechanisms regulate the recruitment of spindle assembly checkpoint proteins to the budding yeast kinetochore
title_sort dual mechanisms regulate the recruitment of spindle assembly checkpoint proteins to the budding yeast kinetochore
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5221577/
https://www.ncbi.nlm.nih.gov/pubmed/27170178
http://dx.doi.org/10.1091/mbc.E16-01-0007
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