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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Cell Biology
2016
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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. |
format | Online Article Text |
id | pubmed-5221577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
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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