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Genetic basis of phenotypic plasticity and genotype × environment interactions in a multi-parental tomato population

Deciphering the genetic basis of phenotypic plasticity and genotype × environment interactions (G×E) is of primary importance for plant breeding in the context of global climate change. Tomato (Solanum lycopersicum) is a widely cultivated crop that can grow in different geographical habitats and tha...

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Autores principales: Diouf, Isidore, Derivot, Laurent, Koussevitzky, Shai, Carretero, Yolande, Bitton, Frédérique, Moreau, Laurence, Causse, Mathilde
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501811/
https://www.ncbi.nlm.nih.gov/pubmed/32474596
http://dx.doi.org/10.1093/jxb/eraa265
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author Diouf, Isidore
Derivot, Laurent
Koussevitzky, Shai
Carretero, Yolande
Bitton, Frédérique
Moreau, Laurence
Causse, Mathilde
author_facet Diouf, Isidore
Derivot, Laurent
Koussevitzky, Shai
Carretero, Yolande
Bitton, Frédérique
Moreau, Laurence
Causse, Mathilde
author_sort Diouf, Isidore
collection PubMed
description Deciphering the genetic basis of phenotypic plasticity and genotype × environment interactions (G×E) is of primary importance for plant breeding in the context of global climate change. Tomato (Solanum lycopersicum) is a widely cultivated crop that can grow in different geographical habitats and that displays a great capacity for expressing phenotypic plasticity. We used a multi-parental advanced generation intercross (MAGIC) tomato population to explore G×E and plasticity for multiple traits measured in a multi-environment trial (MET) comprising optimal cultural conditions together with water deficit, salinity, and heat stress over 12 environments. Substantial G×E was observed for all the traits measured. Different plasticity parameters were estimated by employing Finlay–Wilkinson and factorial regression models and these were used together with genotypic means for quantitative trait loci (QTL) mapping analyses. In addition, mixed linear models were also used to investigate the presence of QTL × environment interactions. The results highlighted a complex genetic architecture of tomato plasticity and G×E. Candidate genes that might be involved in the occurrence of G×E are proposed, paving the way for functional characterization of stress response genes in tomato and for breeding climate-adapted cultivars.
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spelling pubmed-75018112020-09-23 Genetic basis of phenotypic plasticity and genotype × environment interactions in a multi-parental tomato population Diouf, Isidore Derivot, Laurent Koussevitzky, Shai Carretero, Yolande Bitton, Frédérique Moreau, Laurence Causse, Mathilde J Exp Bot Research Papers Deciphering the genetic basis of phenotypic plasticity and genotype × environment interactions (G×E) is of primary importance for plant breeding in the context of global climate change. Tomato (Solanum lycopersicum) is a widely cultivated crop that can grow in different geographical habitats and that displays a great capacity for expressing phenotypic plasticity. We used a multi-parental advanced generation intercross (MAGIC) tomato population to explore G×E and plasticity for multiple traits measured in a multi-environment trial (MET) comprising optimal cultural conditions together with water deficit, salinity, and heat stress over 12 environments. Substantial G×E was observed for all the traits measured. Different plasticity parameters were estimated by employing Finlay–Wilkinson and factorial regression models and these were used together with genotypic means for quantitative trait loci (QTL) mapping analyses. In addition, mixed linear models were also used to investigate the presence of QTL × environment interactions. The results highlighted a complex genetic architecture of tomato plasticity and G×E. Candidate genes that might be involved in the occurrence of G×E are proposed, paving the way for functional characterization of stress response genes in tomato and for breeding climate-adapted cultivars. Oxford University Press 2020-05-31 /pmc/articles/PMC7501811/ /pubmed/32474596 http://dx.doi.org/10.1093/jxb/eraa265 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Experimental Biology. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Papers
Diouf, Isidore
Derivot, Laurent
Koussevitzky, Shai
Carretero, Yolande
Bitton, Frédérique
Moreau, Laurence
Causse, Mathilde
Genetic basis of phenotypic plasticity and genotype × environment interactions in a multi-parental tomato population
title Genetic basis of phenotypic plasticity and genotype × environment interactions in a multi-parental tomato population
title_full Genetic basis of phenotypic plasticity and genotype × environment interactions in a multi-parental tomato population
title_fullStr Genetic basis of phenotypic plasticity and genotype × environment interactions in a multi-parental tomato population
title_full_unstemmed Genetic basis of phenotypic plasticity and genotype × environment interactions in a multi-parental tomato population
title_short Genetic basis of phenotypic plasticity and genotype × environment interactions in a multi-parental tomato population
title_sort genetic basis of phenotypic plasticity and genotype × environment interactions in a multi-parental tomato population
topic Research Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7501811/
https://www.ncbi.nlm.nih.gov/pubmed/32474596
http://dx.doi.org/10.1093/jxb/eraa265
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