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Yeast Growth Plasticity Is Regulated by Environment-Specific Multi-QTL Interactions

For a unicellular, non-motile organism like Saccharomyces cerevisiae, carbon sources act both as nutrients and as signaling molecules and consequently affect various fitness parameters including growth. It is therefore advantageous for yeast strains to adapt their growth to carbon source variation....

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Autores principales: Bhatia, Aatish, Yadav, Anupama, Zhu, Chenchen, Gagneur, Julien, Radhakrishnan, Aparna, Steinmetz, Lars M., Bhanot, Gyan, Sinha, Himanshu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Genetics Society of America 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4025475/
https://www.ncbi.nlm.nih.gov/pubmed/24474169
http://dx.doi.org/10.1534/g3.113.009142
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author Bhatia, Aatish
Yadav, Anupama
Zhu, Chenchen
Gagneur, Julien
Radhakrishnan, Aparna
Steinmetz, Lars M.
Bhanot, Gyan
Sinha, Himanshu
author_facet Bhatia, Aatish
Yadav, Anupama
Zhu, Chenchen
Gagneur, Julien
Radhakrishnan, Aparna
Steinmetz, Lars M.
Bhanot, Gyan
Sinha, Himanshu
author_sort Bhatia, Aatish
collection PubMed
description For a unicellular, non-motile organism like Saccharomyces cerevisiae, carbon sources act both as nutrients and as signaling molecules and consequently affect various fitness parameters including growth. It is therefore advantageous for yeast strains to adapt their growth to carbon source variation. The ability of a given genotype to manifest different phenotypes in varying environments is known as phenotypic plasticity. To identify quantitative trait loci (QTL) that drive plasticity in growth, two growth parameters (growth rate and biomass) were measured in a published dataset from meiotic recombinants of two genetically divergent yeast strains grown in different carbon sources. To identify QTL contributing to plasticity across pairs of environments, gene–environment interaction mapping was performed, which identified several QTL that have a differential effect across environments, some of which act antagonistically across pairs of environments. Multi-QTL analysis identified loci interacting with previously known growth affecting QTL as well as novel two-QTL interactions that affect growth. A QTL that had no significant independent effect was found to alter growth rate and biomass for several carbon sources through two-QTL interactions. Our study demonstrates that environment-specific epistatic interactions contribute to the growth plasticity in yeast. We propose that a targeted scan for epistatic interactions, such as the one described here, can help unravel mechanisms regulating phenotypic plasticity.
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spelling pubmed-40254752014-05-30 Yeast Growth Plasticity Is Regulated by Environment-Specific Multi-QTL Interactions Bhatia, Aatish Yadav, Anupama Zhu, Chenchen Gagneur, Julien Radhakrishnan, Aparna Steinmetz, Lars M. Bhanot, Gyan Sinha, Himanshu G3 (Bethesda) Investigations For a unicellular, non-motile organism like Saccharomyces cerevisiae, carbon sources act both as nutrients and as signaling molecules and consequently affect various fitness parameters including growth. It is therefore advantageous for yeast strains to adapt their growth to carbon source variation. The ability of a given genotype to manifest different phenotypes in varying environments is known as phenotypic plasticity. To identify quantitative trait loci (QTL) that drive plasticity in growth, two growth parameters (growth rate and biomass) were measured in a published dataset from meiotic recombinants of two genetically divergent yeast strains grown in different carbon sources. To identify QTL contributing to plasticity across pairs of environments, gene–environment interaction mapping was performed, which identified several QTL that have a differential effect across environments, some of which act antagonistically across pairs of environments. Multi-QTL analysis identified loci interacting with previously known growth affecting QTL as well as novel two-QTL interactions that affect growth. A QTL that had no significant independent effect was found to alter growth rate and biomass for several carbon sources through two-QTL interactions. Our study demonstrates that environment-specific epistatic interactions contribute to the growth plasticity in yeast. We propose that a targeted scan for epistatic interactions, such as the one described here, can help unravel mechanisms regulating phenotypic plasticity. Genetics Society of America 2014-01-28 /pmc/articles/PMC4025475/ /pubmed/24474169 http://dx.doi.org/10.1534/g3.113.009142 Text en Copyright © 2014 Bhatia et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution Unported License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Investigations
Bhatia, Aatish
Yadav, Anupama
Zhu, Chenchen
Gagneur, Julien
Radhakrishnan, Aparna
Steinmetz, Lars M.
Bhanot, Gyan
Sinha, Himanshu
Yeast Growth Plasticity Is Regulated by Environment-Specific Multi-QTL Interactions
title Yeast Growth Plasticity Is Regulated by Environment-Specific Multi-QTL Interactions
title_full Yeast Growth Plasticity Is Regulated by Environment-Specific Multi-QTL Interactions
title_fullStr Yeast Growth Plasticity Is Regulated by Environment-Specific Multi-QTL Interactions
title_full_unstemmed Yeast Growth Plasticity Is Regulated by Environment-Specific Multi-QTL Interactions
title_short Yeast Growth Plasticity Is Regulated by Environment-Specific Multi-QTL Interactions
title_sort yeast growth plasticity is regulated by environment-specific multi-qtl interactions
topic Investigations
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4025475/
https://www.ncbi.nlm.nih.gov/pubmed/24474169
http://dx.doi.org/10.1534/g3.113.009142
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