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Dearth of polymorphism associated with a sustained response to selection for flowering time in maize
BACKGROUND: Long term selection experiments bring unique insights on the genetic architecture of quantitative traits and their evolvability. Indeed, they are utilized to (i) monitor changes in allele frequencies and assess the effects of genomic regions involved traits determinism; (ii) evaluate the...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4458035/ https://www.ncbi.nlm.nih.gov/pubmed/26049736 http://dx.doi.org/10.1186/s12862-015-0382-5 |
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author | Durand, Eleonore Tenaillon, Maud I Raffoux, Xavier Thépot, Stéphanie Falque, Matthieu Jamin, Philippe Bourgais, Aurélie Ressayre, Adrienne Dillmann, Christine |
author_facet | Durand, Eleonore Tenaillon, Maud I Raffoux, Xavier Thépot, Stéphanie Falque, Matthieu Jamin, Philippe Bourgais, Aurélie Ressayre, Adrienne Dillmann, Christine |
author_sort | Durand, Eleonore |
collection | PubMed |
description | BACKGROUND: Long term selection experiments bring unique insights on the genetic architecture of quantitative traits and their evolvability. Indeed, they are utilized to (i) monitor changes in allele frequencies and assess the effects of genomic regions involved traits determinism; (ii) evaluate the role of standing variation versus new mutations during adaptation; (iii) investigate the contribution of non allelic interactions. Here we describe genetic and phenotypic evolution of two independent Divergent Selection Experiments (DSEs) for flowering time conducted during 16 years from two early maize inbred lines. RESULTS: Our experimental design uses selfing as the mating system and small population sizes, so that two independent families evolved within each population, Late and Early. Observed patterns are strikingly similar between the two DSEs. We observed a significant response to selection in both directions during the first 7 generations of selection. Within Early families, the response is linear through 16 generations, consistent with the maintenance of genetic variance. Within Late families and despite maintenance of significant genetic variation across 17 generations, the response to selection reached a plateau after 7 generations. This plateau is likely caused by physiological limits. Residual heterozygosity in the initial inbreds can partly explain the observed responses as evidenced by 42 markers derived from both Methyl-Sensitive Amplification- and Amplified Fragment Length- Polymorphisms. Among the 42, a subset of 13 markers most of which are in high linkage disequilibrium, display a strong association with flowering time variation. Their fast fixation throughout DSEs’ pedigrees results in strong genetic differentiation between populations and families. CONCLUSIONS: Our results reveal a paradox between the sustainability of the response to selection and the associated dearth of polymorphisms. Among other hypotheses, we discuss the maintenance of heritable variation by few mutations with strong epistatic interactions whose effects are modified by continuous changes of the genetic background through time. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-015-0382-5) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4458035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-44580352015-06-07 Dearth of polymorphism associated with a sustained response to selection for flowering time in maize Durand, Eleonore Tenaillon, Maud I Raffoux, Xavier Thépot, Stéphanie Falque, Matthieu Jamin, Philippe Bourgais, Aurélie Ressayre, Adrienne Dillmann, Christine BMC Evol Biol Research Article BACKGROUND: Long term selection experiments bring unique insights on the genetic architecture of quantitative traits and their evolvability. Indeed, they are utilized to (i) monitor changes in allele frequencies and assess the effects of genomic regions involved traits determinism; (ii) evaluate the role of standing variation versus new mutations during adaptation; (iii) investigate the contribution of non allelic interactions. Here we describe genetic and phenotypic evolution of two independent Divergent Selection Experiments (DSEs) for flowering time conducted during 16 years from two early maize inbred lines. RESULTS: Our experimental design uses selfing as the mating system and small population sizes, so that two independent families evolved within each population, Late and Early. Observed patterns are strikingly similar between the two DSEs. We observed a significant response to selection in both directions during the first 7 generations of selection. Within Early families, the response is linear through 16 generations, consistent with the maintenance of genetic variance. Within Late families and despite maintenance of significant genetic variation across 17 generations, the response to selection reached a plateau after 7 generations. This plateau is likely caused by physiological limits. Residual heterozygosity in the initial inbreds can partly explain the observed responses as evidenced by 42 markers derived from both Methyl-Sensitive Amplification- and Amplified Fragment Length- Polymorphisms. Among the 42, a subset of 13 markers most of which are in high linkage disequilibrium, display a strong association with flowering time variation. Their fast fixation throughout DSEs’ pedigrees results in strong genetic differentiation between populations and families. CONCLUSIONS: Our results reveal a paradox between the sustainability of the response to selection and the associated dearth of polymorphisms. Among other hypotheses, we discuss the maintenance of heritable variation by few mutations with strong epistatic interactions whose effects are modified by continuous changes of the genetic background through time. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12862-015-0382-5) contains supplementary material, which is available to authorized users. BioMed Central 2015-06-07 /pmc/articles/PMC4458035/ /pubmed/26049736 http://dx.doi.org/10.1186/s12862-015-0382-5 Text en © Durand et al. 2015 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 use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Durand, Eleonore Tenaillon, Maud I Raffoux, Xavier Thépot, Stéphanie Falque, Matthieu Jamin, Philippe Bourgais, Aurélie Ressayre, Adrienne Dillmann, Christine Dearth of polymorphism associated with a sustained response to selection for flowering time in maize |
title | Dearth of polymorphism associated with a sustained response to selection for flowering time in maize |
title_full | Dearth of polymorphism associated with a sustained response to selection for flowering time in maize |
title_fullStr | Dearth of polymorphism associated with a sustained response to selection for flowering time in maize |
title_full_unstemmed | Dearth of polymorphism associated with a sustained response to selection for flowering time in maize |
title_short | Dearth of polymorphism associated with a sustained response to selection for flowering time in maize |
title_sort | dearth of polymorphism associated with a sustained response to selection for flowering time in maize |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4458035/ https://www.ncbi.nlm.nih.gov/pubmed/26049736 http://dx.doi.org/10.1186/s12862-015-0382-5 |
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