Cargando…

Adaptation of Maize to Temperate Climates: Mid-Density Genome-Wide Association Genetics and Diversity Patterns Reveal Key Genomic Regions, with a Major Contribution of the Vgt2 (ZCN8) Locus

The migration of maize from tropical to temperate climates was accompanied by a dramatic evolution in flowering time. To gain insight into the genetic architecture of this adaptive trait, we conducted a 50K SNP-based genome-wide association and diversity investigation on a panel of tropical and temp...

Descripción completa

Detalles Bibliográficos
Autores principales: Bouchet, Sophie, Servin, Bertrand, Bertin, Pascal, Madur, Delphine, Combes, Valérie, Dumas, Fabrice, Brunel, Dominique, Laborde, Jacques, Charcosset, Alain, Nicolas, Stéphane
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3758321/
https://www.ncbi.nlm.nih.gov/pubmed/24023610
http://dx.doi.org/10.1371/journal.pone.0071377
_version_ 1782477124046684160
author Bouchet, Sophie
Servin, Bertrand
Bertin, Pascal
Madur, Delphine
Combes, Valérie
Dumas, Fabrice
Brunel, Dominique
Laborde, Jacques
Charcosset, Alain
Nicolas, Stéphane
author_facet Bouchet, Sophie
Servin, Bertrand
Bertin, Pascal
Madur, Delphine
Combes, Valérie
Dumas, Fabrice
Brunel, Dominique
Laborde, Jacques
Charcosset, Alain
Nicolas, Stéphane
author_sort Bouchet, Sophie
collection PubMed
description The migration of maize from tropical to temperate climates was accompanied by a dramatic evolution in flowering time. To gain insight into the genetic architecture of this adaptive trait, we conducted a 50K SNP-based genome-wide association and diversity investigation on a panel of tropical and temperate American and European representatives. Eighteen genomic regions were associated with flowering time. The number of early alleles cumulated along these regions was highly correlated with flowering time. Polymorphism in the vicinity of the ZCN8 gene, which is the closest maize homologue to Arabidopsis major flowering time (FT) gene, had the strongest effect. This polymorphism is in the vicinity of the causal factor of Vgt2 QTL. Diversity was lower, whereas differentiation and LD were higher for associated loci compared to the rest of the genome, which is consistent with selection acting on flowering time during maize migration. Selection tests also revealed supplementary loci that were highly differentiated among groups and not associated with flowering time in our panel, whereas they were in other linkage-based studies. This suggests that allele fixation led to a lack of statistical power when structure and relatedness were taken into account in a linear mixed model. Complementary designs and analysis methods are necessary to unravel the architecture of complex traits. Based on linkage disequilibrium (LD) estimates corrected for population structure, we concluded that the number of SNPs genotyped should be at least doubled to capture all QTLs contributing to the genetic architecture of polygenic traits in this panel. These results show that maize flowering time is controlled by numerous QTLs of small additive effect and that strong polygenic selection occurred under cool climatic conditions. They should contribute to more efficient genomic predictions of flowering time and facilitate the dissemination of diverse maize genetic resources under a wide range of environments.
format Online
Article
Text
id pubmed-3758321
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-37583212013-09-10 Adaptation of Maize to Temperate Climates: Mid-Density Genome-Wide Association Genetics and Diversity Patterns Reveal Key Genomic Regions, with a Major Contribution of the Vgt2 (ZCN8) Locus Bouchet, Sophie Servin, Bertrand Bertin, Pascal Madur, Delphine Combes, Valérie Dumas, Fabrice Brunel, Dominique Laborde, Jacques Charcosset, Alain Nicolas, Stéphane PLoS One Research Article The migration of maize from tropical to temperate climates was accompanied by a dramatic evolution in flowering time. To gain insight into the genetic architecture of this adaptive trait, we conducted a 50K SNP-based genome-wide association and diversity investigation on a panel of tropical and temperate American and European representatives. Eighteen genomic regions were associated with flowering time. The number of early alleles cumulated along these regions was highly correlated with flowering time. Polymorphism in the vicinity of the ZCN8 gene, which is the closest maize homologue to Arabidopsis major flowering time (FT) gene, had the strongest effect. This polymorphism is in the vicinity of the causal factor of Vgt2 QTL. Diversity was lower, whereas differentiation and LD were higher for associated loci compared to the rest of the genome, which is consistent with selection acting on flowering time during maize migration. Selection tests also revealed supplementary loci that were highly differentiated among groups and not associated with flowering time in our panel, whereas they were in other linkage-based studies. This suggests that allele fixation led to a lack of statistical power when structure and relatedness were taken into account in a linear mixed model. Complementary designs and analysis methods are necessary to unravel the architecture of complex traits. Based on linkage disequilibrium (LD) estimates corrected for population structure, we concluded that the number of SNPs genotyped should be at least doubled to capture all QTLs contributing to the genetic architecture of polygenic traits in this panel. These results show that maize flowering time is controlled by numerous QTLs of small additive effect and that strong polygenic selection occurred under cool climatic conditions. They should contribute to more efficient genomic predictions of flowering time and facilitate the dissemination of diverse maize genetic resources under a wide range of environments. Public Library of Science 2013-08-30 /pmc/articles/PMC3758321/ /pubmed/24023610 http://dx.doi.org/10.1371/journal.pone.0071377 Text en © 2013 Bouchet 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
Bouchet, Sophie
Servin, Bertrand
Bertin, Pascal
Madur, Delphine
Combes, Valérie
Dumas, Fabrice
Brunel, Dominique
Laborde, Jacques
Charcosset, Alain
Nicolas, Stéphane
Adaptation of Maize to Temperate Climates: Mid-Density Genome-Wide Association Genetics and Diversity Patterns Reveal Key Genomic Regions, with a Major Contribution of the Vgt2 (ZCN8) Locus
title Adaptation of Maize to Temperate Climates: Mid-Density Genome-Wide Association Genetics and Diversity Patterns Reveal Key Genomic Regions, with a Major Contribution of the Vgt2 (ZCN8) Locus
title_full Adaptation of Maize to Temperate Climates: Mid-Density Genome-Wide Association Genetics and Diversity Patterns Reveal Key Genomic Regions, with a Major Contribution of the Vgt2 (ZCN8) Locus
title_fullStr Adaptation of Maize to Temperate Climates: Mid-Density Genome-Wide Association Genetics and Diversity Patterns Reveal Key Genomic Regions, with a Major Contribution of the Vgt2 (ZCN8) Locus
title_full_unstemmed Adaptation of Maize to Temperate Climates: Mid-Density Genome-Wide Association Genetics and Diversity Patterns Reveal Key Genomic Regions, with a Major Contribution of the Vgt2 (ZCN8) Locus
title_short Adaptation of Maize to Temperate Climates: Mid-Density Genome-Wide Association Genetics and Diversity Patterns Reveal Key Genomic Regions, with a Major Contribution of the Vgt2 (ZCN8) Locus
title_sort adaptation of maize to temperate climates: mid-density genome-wide association genetics and diversity patterns reveal key genomic regions, with a major contribution of the vgt2 (zcn8) locus
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3758321/
https://www.ncbi.nlm.nih.gov/pubmed/24023610
http://dx.doi.org/10.1371/journal.pone.0071377
work_keys_str_mv AT bouchetsophie adaptationofmaizetotemperateclimatesmiddensitygenomewideassociationgeneticsanddiversitypatternsrevealkeygenomicregionswithamajorcontributionofthevgt2zcn8locus
AT servinbertrand adaptationofmaizetotemperateclimatesmiddensitygenomewideassociationgeneticsanddiversitypatternsrevealkeygenomicregionswithamajorcontributionofthevgt2zcn8locus
AT bertinpascal adaptationofmaizetotemperateclimatesmiddensitygenomewideassociationgeneticsanddiversitypatternsrevealkeygenomicregionswithamajorcontributionofthevgt2zcn8locus
AT madurdelphine adaptationofmaizetotemperateclimatesmiddensitygenomewideassociationgeneticsanddiversitypatternsrevealkeygenomicregionswithamajorcontributionofthevgt2zcn8locus
AT combesvalerie adaptationofmaizetotemperateclimatesmiddensitygenomewideassociationgeneticsanddiversitypatternsrevealkeygenomicregionswithamajorcontributionofthevgt2zcn8locus
AT dumasfabrice adaptationofmaizetotemperateclimatesmiddensitygenomewideassociationgeneticsanddiversitypatternsrevealkeygenomicregionswithamajorcontributionofthevgt2zcn8locus
AT bruneldominique adaptationofmaizetotemperateclimatesmiddensitygenomewideassociationgeneticsanddiversitypatternsrevealkeygenomicregionswithamajorcontributionofthevgt2zcn8locus
AT labordejacques adaptationofmaizetotemperateclimatesmiddensitygenomewideassociationgeneticsanddiversitypatternsrevealkeygenomicregionswithamajorcontributionofthevgt2zcn8locus
AT charcossetalain adaptationofmaizetotemperateclimatesmiddensitygenomewideassociationgeneticsanddiversitypatternsrevealkeygenomicregionswithamajorcontributionofthevgt2zcn8locus
AT nicolasstephane adaptationofmaizetotemperateclimatesmiddensitygenomewideassociationgeneticsanddiversitypatternsrevealkeygenomicregionswithamajorcontributionofthevgt2zcn8locus