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Getting to S: CDK functions and targets on the path to cell-cycle commitment

How and when eukaryotic cells make the irrevocable commitment to divide remain central questions in the cell-cycle field. Parallel studies in yeast and mammalian cells seemed to suggest analogous control mechanisms operating during the G1 phase—at Start or the restriction (R) point, respectively—to...

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Detalles Bibliográficos
Autor principal: Fisher, Robert P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000Research 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5040153/
https://www.ncbi.nlm.nih.gov/pubmed/27746911
http://dx.doi.org/10.12688/f1000research.9463.1
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author Fisher, Robert P.
author_facet Fisher, Robert P.
author_sort Fisher, Robert P.
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description How and when eukaryotic cells make the irrevocable commitment to divide remain central questions in the cell-cycle field. Parallel studies in yeast and mammalian cells seemed to suggest analogous control mechanisms operating during the G1 phase—at Start or the restriction (R) point, respectively—to integrate nutritional and developmental signals and decide between distinct cell fates: cell-cycle arrest or exit versus irreversible commitment to a round of division. Recent work has revealed molecular mechanisms underlying this decision-making process in both yeast and mammalian cells but also cast doubt on the nature and timing of cell-cycle commitment in multicellular organisms. These studies suggest an expanded temporal window of mitogen sensing under certain growth conditions, illuminate unexpected obstacles and exit ramps on the path to full cell-cycle commitment, and raise new questions regarding the functions of cyclin-dependent kinases (CDKs) that drive G1 progression and S-phase entry.
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spelling pubmed-50401532016-10-13 Getting to S: CDK functions and targets on the path to cell-cycle commitment Fisher, Robert P. F1000Res Review How and when eukaryotic cells make the irrevocable commitment to divide remain central questions in the cell-cycle field. Parallel studies in yeast and mammalian cells seemed to suggest analogous control mechanisms operating during the G1 phase—at Start or the restriction (R) point, respectively—to integrate nutritional and developmental signals and decide between distinct cell fates: cell-cycle arrest or exit versus irreversible commitment to a round of division. Recent work has revealed molecular mechanisms underlying this decision-making process in both yeast and mammalian cells but also cast doubt on the nature and timing of cell-cycle commitment in multicellular organisms. These studies suggest an expanded temporal window of mitogen sensing under certain growth conditions, illuminate unexpected obstacles and exit ramps on the path to full cell-cycle commitment, and raise new questions regarding the functions of cyclin-dependent kinases (CDKs) that drive G1 progression and S-phase entry. F1000Research 2016-09-26 /pmc/articles/PMC5040153/ /pubmed/27746911 http://dx.doi.org/10.12688/f1000research.9463.1 Text en Copyright: © 2016 Fisher RP http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Fisher, Robert P.
Getting to S: CDK functions and targets on the path to cell-cycle commitment
title Getting to S: CDK functions and targets on the path to cell-cycle commitment
title_full Getting to S: CDK functions and targets on the path to cell-cycle commitment
title_fullStr Getting to S: CDK functions and targets on the path to cell-cycle commitment
title_full_unstemmed Getting to S: CDK functions and targets on the path to cell-cycle commitment
title_short Getting to S: CDK functions and targets on the path to cell-cycle commitment
title_sort getting to s: cdk functions and targets on the path to cell-cycle commitment
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5040153/
https://www.ncbi.nlm.nih.gov/pubmed/27746911
http://dx.doi.org/10.12688/f1000research.9463.1
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