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Cell cycle Start is coupled to entry into the yeast metabolic cycle across diverse strains and growth rates
Cells have evolved oscillators with different frequencies to coordinate periodic processes. Here we studied the interaction of two oscillators, the cell division cycle (CDC) and the yeast metabolic cycle (YMC), in budding yeast. Previous work suggested that the CDC and YMC interact to separate high...
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/PMC4694762/ https://www.ncbi.nlm.nih.gov/pubmed/26538026 http://dx.doi.org/10.1091/mbc.E15-07-0454 |
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author | Burnetti, Anthony J. Aydin, Mert Buchler, Nicolas E. |
author_facet | Burnetti, Anthony J. Aydin, Mert Buchler, Nicolas E. |
author_sort | Burnetti, Anthony J. |
collection | PubMed |
description | Cells have evolved oscillators with different frequencies to coordinate periodic processes. Here we studied the interaction of two oscillators, the cell division cycle (CDC) and the yeast metabolic cycle (YMC), in budding yeast. Previous work suggested that the CDC and YMC interact to separate high oxygen consumption (HOC) from DNA replication to prevent genetic damage. To test this hypothesis, we grew diverse strains in chemostat and measured DNA replication and oxygen consumption with high temporal resolution at different growth rates. Our data showed that HOC is not strictly separated from DNA replication; rather, cell cycle Start is coupled with the initiation of HOC and catabolism of storage carbohydrates. The logic of this YMC–CDC coupling may be to ensure that DNA replication and cell division occur only when sufficient cellular energy reserves have accumulated. Our results also uncovered a quantitative relationship between CDC period and YMC period across different strains. More generally, our approach shows how studies in genetically diverse strains efficiently identify robust phenotypes and steer the experimentalist away from strain-specific idiosyncrasies. |
format | Online Article Text |
id | pubmed-4694762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | The American Society for Cell Biology |
record_format | MEDLINE/PubMed |
spelling | pubmed-46947622016-03-16 Cell cycle Start is coupled to entry into the yeast metabolic cycle across diverse strains and growth rates Burnetti, Anthony J. Aydin, Mert Buchler, Nicolas E. Mol Biol Cell Articles Cells have evolved oscillators with different frequencies to coordinate periodic processes. Here we studied the interaction of two oscillators, the cell division cycle (CDC) and the yeast metabolic cycle (YMC), in budding yeast. Previous work suggested that the CDC and YMC interact to separate high oxygen consumption (HOC) from DNA replication to prevent genetic damage. To test this hypothesis, we grew diverse strains in chemostat and measured DNA replication and oxygen consumption with high temporal resolution at different growth rates. Our data showed that HOC is not strictly separated from DNA replication; rather, cell cycle Start is coupled with the initiation of HOC and catabolism of storage carbohydrates. The logic of this YMC–CDC coupling may be to ensure that DNA replication and cell division occur only when sufficient cellular energy reserves have accumulated. Our results also uncovered a quantitative relationship between CDC period and YMC period across different strains. More generally, our approach shows how studies in genetically diverse strains efficiently identify robust phenotypes and steer the experimentalist away from strain-specific idiosyncrasies. The American Society for Cell Biology 2016-01-01 /pmc/articles/PMC4694762/ /pubmed/26538026 http://dx.doi.org/10.1091/mbc.E15-07-0454 Text en © 2016 Burnetti 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 Burnetti, Anthony J. Aydin, Mert Buchler, Nicolas E. Cell cycle Start is coupled to entry into the yeast metabolic cycle across diverse strains and growth rates |
title | Cell cycle Start is coupled to entry into the yeast metabolic cycle across diverse strains and growth rates |
title_full | Cell cycle Start is coupled to entry into the yeast metabolic cycle across diverse strains and growth rates |
title_fullStr | Cell cycle Start is coupled to entry into the yeast metabolic cycle across diverse strains and growth rates |
title_full_unstemmed | Cell cycle Start is coupled to entry into the yeast metabolic cycle across diverse strains and growth rates |
title_short | Cell cycle Start is coupled to entry into the yeast metabolic cycle across diverse strains and growth rates |
title_sort | cell cycle start is coupled to entry into the yeast metabolic cycle across diverse strains and growth rates |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4694762/ https://www.ncbi.nlm.nih.gov/pubmed/26538026 http://dx.doi.org/10.1091/mbc.E15-07-0454 |
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