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How the cell cycle clock ticks

Eukaryotic cell division has been studied thoroughly and is understood in great mechanistic detail. Paradoxically, however, we lack an understanding of its core control process, in which the master regulator of the cell cycle, cyclin-dependent kinase (CDK), temporally coordinates an array of complex...

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Autores principales: Örd, Mihkel, Loog, Mart
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Cell Biology 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6589557/
https://www.ncbi.nlm.nih.gov/pubmed/30640587
http://dx.doi.org/10.1091/mbc.E18-05-0272
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author Örd, Mihkel
Loog, Mart
author_facet Örd, Mihkel
Loog, Mart
author_sort Örd, Mihkel
collection PubMed
description Eukaryotic cell division has been studied thoroughly and is understood in great mechanistic detail. Paradoxically, however, we lack an understanding of its core control process, in which the master regulator of the cell cycle, cyclin-dependent kinase (CDK), temporally coordinates an array of complex molecular events. The core elements of the CDK control system are conserved in eukaryotic cells, which contain multiple cyclin–CDK forms that have poorly defined and partially overlapping responsibilities in the cell cycle. However, a single CDK can drive all events of cell division in both mammalian and yeast cells, and in fission yeast a single mitotic cyclin can drive the cell cycle without major problems. But how can the same CDK induce different events when activated at different times during the cell cycle? This question, which has bewildered cell cycle researchers for decades, now has a sufficiently clear mechanistic answer. This Perspective aims to provide a synthesis of recent data to facilitate a better understanding of this central cellular control system.
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spelling pubmed-65895572019-06-28 How the cell cycle clock ticks Örd, Mihkel Loog, Mart Mol Biol Cell Perspectives Eukaryotic cell division has been studied thoroughly and is understood in great mechanistic detail. Paradoxically, however, we lack an understanding of its core control process, in which the master regulator of the cell cycle, cyclin-dependent kinase (CDK), temporally coordinates an array of complex molecular events. The core elements of the CDK control system are conserved in eukaryotic cells, which contain multiple cyclin–CDK forms that have poorly defined and partially overlapping responsibilities in the cell cycle. However, a single CDK can drive all events of cell division in both mammalian and yeast cells, and in fission yeast a single mitotic cyclin can drive the cell cycle without major problems. But how can the same CDK induce different events when activated at different times during the cell cycle? This question, which has bewildered cell cycle researchers for decades, now has a sufficiently clear mechanistic answer. This Perspective aims to provide a synthesis of recent data to facilitate a better understanding of this central cellular control system. The American Society for Cell Biology 2019-01-15 /pmc/articles/PMC6589557/ /pubmed/30640587 http://dx.doi.org/10.1091/mbc.E18-05-0272 Text en © 2019 Örd and Loog. “ASCB®,” “The American Society for Cell Biology®,” and “Molecular Biology of the Cell®” are registered trademarks of The American Society for Cell Biology. http://creativecommons.org/licenses/by-nc-sa/3.0 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.
spellingShingle Perspectives
Örd, Mihkel
Loog, Mart
How the cell cycle clock ticks
title How the cell cycle clock ticks
title_full How the cell cycle clock ticks
title_fullStr How the cell cycle clock ticks
title_full_unstemmed How the cell cycle clock ticks
title_short How the cell cycle clock ticks
title_sort how the cell cycle clock ticks
topic Perspectives
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6589557/
https://www.ncbi.nlm.nih.gov/pubmed/30640587
http://dx.doi.org/10.1091/mbc.E18-05-0272
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