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Cellular Plasticity Enables Adaptation to Unforeseen Cell-Cycle Rewiring Challenges

The fundamental dynamics of the cell cycle, underlying cell growth and reproduction, were previously found to be robust under a wide range of environmental and internal perturbations. This property was commonly attributed to its network structure, which enables the coordinated interactions among hun...

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Autores principales: Katzir, Yair, Stolovicki, Elad, Stern, Shay, Braun, Erez
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3445480/
https://www.ncbi.nlm.nih.gov/pubmed/23028834
http://dx.doi.org/10.1371/journal.pone.0045184
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author Katzir, Yair
Stolovicki, Elad
Stern, Shay
Braun, Erez
author_facet Katzir, Yair
Stolovicki, Elad
Stern, Shay
Braun, Erez
author_sort Katzir, Yair
collection PubMed
description The fundamental dynamics of the cell cycle, underlying cell growth and reproduction, were previously found to be robust under a wide range of environmental and internal perturbations. This property was commonly attributed to its network structure, which enables the coordinated interactions among hundreds of proteins. Despite significant advances in deciphering the components and autonomous interactions of this network, understanding the interfaces of the cell cycle with other major cellular processes is still lacking. To gain insight into these interfaces, we used the process of genome-rewiring in yeast by placing an essential metabolic gene HIS3 from the histidine biosynthesis pathway, under the exclusive regulation of different cell-cycle promoters. In a medium lacking histidine and under partial inhibition of the HIS3p, the rewired cells encountered an unforeseen multitasking challenge; the cell-cycle regulatory genes were required to regulate the essential histidine-pathway gene in concert with the other metabolic demands, while simultaneously driving the cell cycle through its proper temporal phases. We show here that chemostat cell populations with rewired cell-cycle promoters adapted within a short time to accommodate the inhibition of HIS3p and stabilized a new phenotypic state. Furthermore, a significant fraction of the population was able to adapt and grow into mature colonies on plates under such inhibiting conditions. The adapted state was shown to be stably inherited across generations. These adaptation dynamics were accompanied by a non-specific and irreproducible genome-wide transcriptional response. Adaptation of the cell-cycle attests to its multitasking capabilities and flexible interface with cellular metabolic processes and requirements. Similar adaptation features were found in our previous work when rewiring HIS3 to the GAL system and switching cells from galactose to glucose. Thus, at the basis of cellular plasticity is the emergence of a yet-unknown general, non-specific mechanism allowing fast inherited adaptation to unforeseen challenges.
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spelling pubmed-34454802012-10-01 Cellular Plasticity Enables Adaptation to Unforeseen Cell-Cycle Rewiring Challenges Katzir, Yair Stolovicki, Elad Stern, Shay Braun, Erez PLoS One Research Article The fundamental dynamics of the cell cycle, underlying cell growth and reproduction, were previously found to be robust under a wide range of environmental and internal perturbations. This property was commonly attributed to its network structure, which enables the coordinated interactions among hundreds of proteins. Despite significant advances in deciphering the components and autonomous interactions of this network, understanding the interfaces of the cell cycle with other major cellular processes is still lacking. To gain insight into these interfaces, we used the process of genome-rewiring in yeast by placing an essential metabolic gene HIS3 from the histidine biosynthesis pathway, under the exclusive regulation of different cell-cycle promoters. In a medium lacking histidine and under partial inhibition of the HIS3p, the rewired cells encountered an unforeseen multitasking challenge; the cell-cycle regulatory genes were required to regulate the essential histidine-pathway gene in concert with the other metabolic demands, while simultaneously driving the cell cycle through its proper temporal phases. We show here that chemostat cell populations with rewired cell-cycle promoters adapted within a short time to accommodate the inhibition of HIS3p and stabilized a new phenotypic state. Furthermore, a significant fraction of the population was able to adapt and grow into mature colonies on plates under such inhibiting conditions. The adapted state was shown to be stably inherited across generations. These adaptation dynamics were accompanied by a non-specific and irreproducible genome-wide transcriptional response. Adaptation of the cell-cycle attests to its multitasking capabilities and flexible interface with cellular metabolic processes and requirements. Similar adaptation features were found in our previous work when rewiring HIS3 to the GAL system and switching cells from galactose to glucose. Thus, at the basis of cellular plasticity is the emergence of a yet-unknown general, non-specific mechanism allowing fast inherited adaptation to unforeseen challenges. Public Library of Science 2012-09-18 /pmc/articles/PMC3445480/ /pubmed/23028834 http://dx.doi.org/10.1371/journal.pone.0045184 Text en © 2012 Katzir 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Katzir, Yair
Stolovicki, Elad
Stern, Shay
Braun, Erez
Cellular Plasticity Enables Adaptation to Unforeseen Cell-Cycle Rewiring Challenges
title Cellular Plasticity Enables Adaptation to Unforeseen Cell-Cycle Rewiring Challenges
title_full Cellular Plasticity Enables Adaptation to Unforeseen Cell-Cycle Rewiring Challenges
title_fullStr Cellular Plasticity Enables Adaptation to Unforeseen Cell-Cycle Rewiring Challenges
title_full_unstemmed Cellular Plasticity Enables Adaptation to Unforeseen Cell-Cycle Rewiring Challenges
title_short Cellular Plasticity Enables Adaptation to Unforeseen Cell-Cycle Rewiring Challenges
title_sort cellular plasticity enables adaptation to unforeseen cell-cycle rewiring challenges
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3445480/
https://www.ncbi.nlm.nih.gov/pubmed/23028834
http://dx.doi.org/10.1371/journal.pone.0045184
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