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Relationship of spindle assembly checkpoint fidelity to species body mass, lifespan, and developmental rate

We have examined the tolerance of the spindle assembly checkpoint (SAC), as measured by the appearance of tetraploid cells in the presence of a microtubule inhibitor, in a series of primary cell strains derived from species with diverse lifespan and body size. We find that the integrity of the SAC v...

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Autores principales: Lorenzini, Antonello, Fink, Lauren S., Stamato, Thomas, Torres, Claudio, Sell, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Impact Journals LLC 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3273901/
https://www.ncbi.nlm.nih.gov/pubmed/22201071
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author Lorenzini, Antonello
Fink, Lauren S.
Stamato, Thomas
Torres, Claudio
Sell, Christian
author_facet Lorenzini, Antonello
Fink, Lauren S.
Stamato, Thomas
Torres, Claudio
Sell, Christian
author_sort Lorenzini, Antonello
collection PubMed
description We have examined the tolerance of the spindle assembly checkpoint (SAC), as measured by the appearance of tetraploid cells in the presence of a microtubule inhibitor, in a series of primary cell strains derived from species with diverse lifespan and body size. We find that the integrity of the SAC varies among these species. There is a robust correlation between the integrity of the SAC and body size, but poor correlation with longevity and parameters of species development (i.e., time of female fertility, gestation length, and postnatal growth rate). The results suggest that fidelity of the SAC co-evolved more closely with the number of mitoses needed to reach adulthood than with species lifespan.
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spelling pubmed-32739012012-02-14 Relationship of spindle assembly checkpoint fidelity to species body mass, lifespan, and developmental rate Lorenzini, Antonello Fink, Lauren S. Stamato, Thomas Torres, Claudio Sell, Christian Aging (Albany NY) Research Paper We have examined the tolerance of the spindle assembly checkpoint (SAC), as measured by the appearance of tetraploid cells in the presence of a microtubule inhibitor, in a series of primary cell strains derived from species with diverse lifespan and body size. We find that the integrity of the SAC varies among these species. There is a robust correlation between the integrity of the SAC and body size, but poor correlation with longevity and parameters of species development (i.e., time of female fertility, gestation length, and postnatal growth rate). The results suggest that fidelity of the SAC co-evolved more closely with the number of mitoses needed to reach adulthood than with species lifespan. Impact Journals LLC 2011-12-26 /pmc/articles/PMC3273901/ /pubmed/22201071 Text en Copyright: © 2011 Lorenzini et al. http://creativecommons.org/licenses/by/2.5/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
spellingShingle Research Paper
Lorenzini, Antonello
Fink, Lauren S.
Stamato, Thomas
Torres, Claudio
Sell, Christian
Relationship of spindle assembly checkpoint fidelity to species body mass, lifespan, and developmental rate
title Relationship of spindle assembly checkpoint fidelity to species body mass, lifespan, and developmental rate
title_full Relationship of spindle assembly checkpoint fidelity to species body mass, lifespan, and developmental rate
title_fullStr Relationship of spindle assembly checkpoint fidelity to species body mass, lifespan, and developmental rate
title_full_unstemmed Relationship of spindle assembly checkpoint fidelity to species body mass, lifespan, and developmental rate
title_short Relationship of spindle assembly checkpoint fidelity to species body mass, lifespan, and developmental rate
title_sort relationship of spindle assembly checkpoint fidelity to species body mass, lifespan, and developmental rate
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3273901/
https://www.ncbi.nlm.nih.gov/pubmed/22201071
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