Cargando…

A size-invariant bud-duration timer enables robustness in yeast cell size control

Cell populations across nearly all forms of life generally maintain a characteristic cell type-dependent size, but how size control is achieved has been a long-standing question. The G1/S boundary of the cell cycle serves as a major point of size control, and mechanisms operating here restrict passa...

Descripción completa

Detalles Bibliográficos
Autores principales: Allard, Corey A. H., Decker, Franziska, Weiner, Orion D., Toettcher, Jared E., Graziano, Brian R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303054/
https://www.ncbi.nlm.nih.gov/pubmed/30576342
http://dx.doi.org/10.1371/journal.pone.0209301
_version_ 1783382107139080192
author Allard, Corey A. H.
Decker, Franziska
Weiner, Orion D.
Toettcher, Jared E.
Graziano, Brian R.
author_facet Allard, Corey A. H.
Decker, Franziska
Weiner, Orion D.
Toettcher, Jared E.
Graziano, Brian R.
author_sort Allard, Corey A. H.
collection PubMed
description Cell populations across nearly all forms of life generally maintain a characteristic cell type-dependent size, but how size control is achieved has been a long-standing question. The G1/S boundary of the cell cycle serves as a major point of size control, and mechanisms operating here restrict passage of cells to Start if they are too small. In contrast, it is less clear how size is regulated post-Start, during S/G2/M. To gain further insight into post-Start size control, we prepared budding yeast that can be reversibly blocked from bud initiation. While blocked, cells continue to grow isotropically, increasing their volume by more than an order of magnitude over unperturbed cells. Upon release from their block, giant mothers reenter the cell cycle and their progeny rapidly return to the original unperturbed size. We found this behavior to be consistent with a size-invariant ‘timer’ specifying the duration of S/G2/M. These results indicate that yeast use at least two distinct mechanisms at different cell cycle phases to ensure size homeostasis.
format Online
Article
Text
id pubmed-6303054
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-63030542019-01-08 A size-invariant bud-duration timer enables robustness in yeast cell size control Allard, Corey A. H. Decker, Franziska Weiner, Orion D. Toettcher, Jared E. Graziano, Brian R. PLoS One Research Article Cell populations across nearly all forms of life generally maintain a characteristic cell type-dependent size, but how size control is achieved has been a long-standing question. The G1/S boundary of the cell cycle serves as a major point of size control, and mechanisms operating here restrict passage of cells to Start if they are too small. In contrast, it is less clear how size is regulated post-Start, during S/G2/M. To gain further insight into post-Start size control, we prepared budding yeast that can be reversibly blocked from bud initiation. While blocked, cells continue to grow isotropically, increasing their volume by more than an order of magnitude over unperturbed cells. Upon release from their block, giant mothers reenter the cell cycle and their progeny rapidly return to the original unperturbed size. We found this behavior to be consistent with a size-invariant ‘timer’ specifying the duration of S/G2/M. These results indicate that yeast use at least two distinct mechanisms at different cell cycle phases to ensure size homeostasis. Public Library of Science 2018-12-21 /pmc/articles/PMC6303054/ /pubmed/30576342 http://dx.doi.org/10.1371/journal.pone.0209301 Text en © 2018 Allard et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Allard, Corey A. H.
Decker, Franziska
Weiner, Orion D.
Toettcher, Jared E.
Graziano, Brian R.
A size-invariant bud-duration timer enables robustness in yeast cell size control
title A size-invariant bud-duration timer enables robustness in yeast cell size control
title_full A size-invariant bud-duration timer enables robustness in yeast cell size control
title_fullStr A size-invariant bud-duration timer enables robustness in yeast cell size control
title_full_unstemmed A size-invariant bud-duration timer enables robustness in yeast cell size control
title_short A size-invariant bud-duration timer enables robustness in yeast cell size control
title_sort size-invariant bud-duration timer enables robustness in yeast cell size control
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6303054/
https://www.ncbi.nlm.nih.gov/pubmed/30576342
http://dx.doi.org/10.1371/journal.pone.0209301
work_keys_str_mv AT allardcoreyah asizeinvariantbuddurationtimerenablesrobustnessinyeastcellsizecontrol
AT deckerfranziska asizeinvariantbuddurationtimerenablesrobustnessinyeastcellsizecontrol
AT weineroriond asizeinvariantbuddurationtimerenablesrobustnessinyeastcellsizecontrol
AT toettcherjarede asizeinvariantbuddurationtimerenablesrobustnessinyeastcellsizecontrol
AT grazianobrianr asizeinvariantbuddurationtimerenablesrobustnessinyeastcellsizecontrol
AT allardcoreyah sizeinvariantbuddurationtimerenablesrobustnessinyeastcellsizecontrol
AT deckerfranziska sizeinvariantbuddurationtimerenablesrobustnessinyeastcellsizecontrol
AT weineroriond sizeinvariantbuddurationtimerenablesrobustnessinyeastcellsizecontrol
AT toettcherjarede sizeinvariantbuddurationtimerenablesrobustnessinyeastcellsizecontrol
AT grazianobrianr sizeinvariantbuddurationtimerenablesrobustnessinyeastcellsizecontrol