Resource plasticity-driven carbon-nitrogen budgeting enables specialization and division of labor in a clonal community

Previously, we found that in glucose-limited Saccharomyces cerevisiae colonies, metabolic constraints drive cells into groups exhibiting gluconeogenic or glycolytic states. In that study, threshold amounts of trehalose - a limiting, produced carbon-resource, controls the emergence and self-organizat...

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Main Authors: Sriram Varahan, Vaibhhav Sinha, Adhish Walvekar, Sandeep Krishna, Sunil Laxman
Format: Article
Language:English
Published: eLife Sciences Publications Ltd 2020-09-01
Series:eLife
Subjects:
Online Access:https://elifesciences.org/articles/57609
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author Sriram Varahan
Vaibhhav Sinha
Adhish Walvekar
Sandeep Krishna
Sunil Laxman
author_facet Sriram Varahan
Vaibhhav Sinha
Adhish Walvekar
Sandeep Krishna
Sunil Laxman
author_sort Sriram Varahan
collection DOAJ
description Previously, we found that in glucose-limited Saccharomyces cerevisiae colonies, metabolic constraints drive cells into groups exhibiting gluconeogenic or glycolytic states. In that study, threshold amounts of trehalose - a limiting, produced carbon-resource, controls the emergence and self-organization of cells exhibiting the glycolytic state, serving as a carbon source that fuels glycolysis (Varahan et al., 2019). We now discover that the plasticity of use of a non-limiting resource, aspartate, controls both resource production and the emergence of heterogeneous cell states, based on differential metabolic budgeting. In gluconeogenic cells, aspartate is a carbon source for trehalose production, while in glycolytic cells using trehalose for carbon, aspartate is predominantly a nitrogen source for nucleotide synthesis. This metabolic plasticity of aspartate enables carbon-nitrogen budgeting, thereby driving the biochemical self-organization of distinct cell states. Through this organization, cells in each state exhibit true division of labor, providing growth/survival advantages for the whole community.
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spelling doaj.art-ca1b8dbbedb04f29a6a2f576d5dec48e2022-12-22T03:52:07ZengeLife Sciences Publications LtdeLife2050-084X2020-09-01910.7554/eLife.57609Resource plasticity-driven carbon-nitrogen budgeting enables specialization and division of labor in a clonal communitySriram Varahan0https://orcid.org/0000-0002-3609-4032Vaibhhav Sinha1https://orcid.org/0000-0002-5169-5485Adhish Walvekar2https://orcid.org/0000-0001-7344-7653Sandeep Krishna3https://orcid.org/0000-0002-0581-173XSunil Laxman4https://orcid.org/0000-0002-0861-5080InStem - Institute for Stem Cell Science and Regenerative Medicine, Bangalore, IndiaSimons Centre for the Study of Living Machines, National Center for Biological Sciences, Tata Institute for Fundamental Research, Bangalore, India; Manipal Academy of Higher Education, Manipal, IndiaInStem - Institute for Stem Cell Science and Regenerative Medicine, Bangalore, IndiaSimons Centre for the Study of Living Machines, National Center for Biological Sciences, Tata Institute for Fundamental Research, Bangalore, IndiaInStem - Institute for Stem Cell Science and Regenerative Medicine, Bangalore, IndiaPreviously, we found that in glucose-limited Saccharomyces cerevisiae colonies, metabolic constraints drive cells into groups exhibiting gluconeogenic or glycolytic states. In that study, threshold amounts of trehalose - a limiting, produced carbon-resource, controls the emergence and self-organization of cells exhibiting the glycolytic state, serving as a carbon source that fuels glycolysis (Varahan et al., 2019). We now discover that the plasticity of use of a non-limiting resource, aspartate, controls both resource production and the emergence of heterogeneous cell states, based on differential metabolic budgeting. In gluconeogenic cells, aspartate is a carbon source for trehalose production, while in glycolytic cells using trehalose for carbon, aspartate is predominantly a nitrogen source for nucleotide synthesis. This metabolic plasticity of aspartate enables carbon-nitrogen budgeting, thereby driving the biochemical self-organization of distinct cell states. Through this organization, cells in each state exhibit true division of labor, providing growth/survival advantages for the whole community.https://elifesciences.org/articles/57609division of laborself-organizationaspartatecross-feedingglycolysistrehalose
spellingShingle Sriram Varahan
Vaibhhav Sinha
Adhish Walvekar
Sandeep Krishna
Sunil Laxman
Resource plasticity-driven carbon-nitrogen budgeting enables specialization and division of labor in a clonal community
eLife
division of labor
self-organization
aspartate
cross-feeding
glycolysis
trehalose
title Resource plasticity-driven carbon-nitrogen budgeting enables specialization and division of labor in a clonal community
title_full Resource plasticity-driven carbon-nitrogen budgeting enables specialization and division of labor in a clonal community
title_fullStr Resource plasticity-driven carbon-nitrogen budgeting enables specialization and division of labor in a clonal community
title_full_unstemmed Resource plasticity-driven carbon-nitrogen budgeting enables specialization and division of labor in a clonal community
title_short Resource plasticity-driven carbon-nitrogen budgeting enables specialization and division of labor in a clonal community
title_sort resource plasticity driven carbon nitrogen budgeting enables specialization and division of labor in a clonal community
topic division of labor
self-organization
aspartate
cross-feeding
glycolysis
trehalose
url https://elifesciences.org/articles/57609
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AT sandeepkrishna resourceplasticitydrivencarbonnitrogenbudgetingenablesspecializationanddivisionoflaborinaclonalcommunity
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