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Artificial selection reveals complex genetic architecture of shoot branching and its response to nitrate supply in Arabidopsis
Quantitative traits may be controlled by many loci, many alleles at each locus, and subject to genotype-by-environment interactions, making them difficult to map. One example of such a complex trait is shoot branching in the model plant Arabidopsis, and its plasticity in response to nitrate. Here, w...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10482290/ https://www.ncbi.nlm.nih.gov/pubmed/37616321 http://dx.doi.org/10.1371/journal.pgen.1010863 |
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author | Tavares, Hugo Readshaw, Anne Kania, Urszula de Jong, Maaike Pasam, Raj K. McCulloch, Hayley Ward, Sally Shenhav, Liron Forsyth, Elizabeth Leyser, Ottoline |
author_facet | Tavares, Hugo Readshaw, Anne Kania, Urszula de Jong, Maaike Pasam, Raj K. McCulloch, Hayley Ward, Sally Shenhav, Liron Forsyth, Elizabeth Leyser, Ottoline |
author_sort | Tavares, Hugo |
collection | PubMed |
description | Quantitative traits may be controlled by many loci, many alleles at each locus, and subject to genotype-by-environment interactions, making them difficult to map. One example of such a complex trait is shoot branching in the model plant Arabidopsis, and its plasticity in response to nitrate. Here, we use artificial selection under contrasting nitrate supplies to dissect the genetic architecture of this complex trait, where loci identified by association mapping failed to explain heritability estimates. We found a consistent response to selection for high branching, with correlated responses in other traits such as plasticity and flowering time. Genome-wide scans for selection and simulations suggest that at least tens of loci control this trait, with a distinct genetic architecture between low and high nitrate treatments. While signals of selection could be detected in the populations selected for high branching on low nitrate, there was very little overlap in the regions selected in three independent populations. Thus the regulatory network controlling shoot branching can be tuned in different ways to give similar phenotypes. |
format | Online Article Text |
id | pubmed-10482290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-104822902023-09-07 Artificial selection reveals complex genetic architecture of shoot branching and its response to nitrate supply in Arabidopsis Tavares, Hugo Readshaw, Anne Kania, Urszula de Jong, Maaike Pasam, Raj K. McCulloch, Hayley Ward, Sally Shenhav, Liron Forsyth, Elizabeth Leyser, Ottoline PLoS Genet Research Article Quantitative traits may be controlled by many loci, many alleles at each locus, and subject to genotype-by-environment interactions, making them difficult to map. One example of such a complex trait is shoot branching in the model plant Arabidopsis, and its plasticity in response to nitrate. Here, we use artificial selection under contrasting nitrate supplies to dissect the genetic architecture of this complex trait, where loci identified by association mapping failed to explain heritability estimates. We found a consistent response to selection for high branching, with correlated responses in other traits such as plasticity and flowering time. Genome-wide scans for selection and simulations suggest that at least tens of loci control this trait, with a distinct genetic architecture between low and high nitrate treatments. While signals of selection could be detected in the populations selected for high branching on low nitrate, there was very little overlap in the regions selected in three independent populations. Thus the regulatory network controlling shoot branching can be tuned in different ways to give similar phenotypes. Public Library of Science 2023-08-24 /pmc/articles/PMC10482290/ /pubmed/37616321 http://dx.doi.org/10.1371/journal.pgen.1010863 Text en © 2023 Tavares et al https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Tavares, Hugo Readshaw, Anne Kania, Urszula de Jong, Maaike Pasam, Raj K. McCulloch, Hayley Ward, Sally Shenhav, Liron Forsyth, Elizabeth Leyser, Ottoline Artificial selection reveals complex genetic architecture of shoot branching and its response to nitrate supply in Arabidopsis |
title | Artificial selection reveals complex genetic architecture of shoot branching and its response to nitrate supply in Arabidopsis |
title_full | Artificial selection reveals complex genetic architecture of shoot branching and its response to nitrate supply in Arabidopsis |
title_fullStr | Artificial selection reveals complex genetic architecture of shoot branching and its response to nitrate supply in Arabidopsis |
title_full_unstemmed | Artificial selection reveals complex genetic architecture of shoot branching and its response to nitrate supply in Arabidopsis |
title_short | Artificial selection reveals complex genetic architecture of shoot branching and its response to nitrate supply in Arabidopsis |
title_sort | artificial selection reveals complex genetic architecture of shoot branching and its response to nitrate supply in arabidopsis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10482290/ https://www.ncbi.nlm.nih.gov/pubmed/37616321 http://dx.doi.org/10.1371/journal.pgen.1010863 |
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