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Genome-wide association mapping of growth dynamics detects time-specific and general quantitative trait loci
Growth is a complex trait determined by the interplay between many genes, some of which play a role at a specific moment during development whereas others play a more general role. To identify the genetic basis of growth, natural variation in Arabidopsis rosette growth was followed in 324 accessions...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585414/ https://www.ncbi.nlm.nih.gov/pubmed/25922493 http://dx.doi.org/10.1093/jxb/erv176 |
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author | Bac-Molenaar, Johanna A. Vreugdenhil, Dick Granier, Christine Keurentjes, Joost J.B. |
author_facet | Bac-Molenaar, Johanna A. Vreugdenhil, Dick Granier, Christine Keurentjes, Joost J.B. |
author_sort | Bac-Molenaar, Johanna A. |
collection | PubMed |
description | Growth is a complex trait determined by the interplay between many genes, some of which play a role at a specific moment during development whereas others play a more general role. To identify the genetic basis of growth, natural variation in Arabidopsis rosette growth was followed in 324 accessions by a combination of top-view imaging, high-throughput image analysis, modelling of growth dynamics, and end-point fresh weight determination. Genome-wide association (GWA) mapping of the temporal growth data resulted in the detection of time-specific quantitative trait loci (QTLs), whereas mapping of model parameters resulted in another set of QTLs related to the whole growth curve. The positive correlation between projected leaf area (PLA) at different time points during the course of the experiment suggested the existence of general growth factors with a function in multiple developmental stages or with prolonged downstream effects. Many QTLs could not be identified when growth was evaluated only at a single time point. Eleven candidate genes were identified, which were annotated to be involved in the determination of cell number and size, seed germination, embryo development, developmental phase transition, or senescence. For eight of these, a mutant or overexpression phenotype related to growth has been reported, supporting the identification of true positives. In addition, the detection of QTLs without obvious candidate genes implies the annotation of novel functions for underlying genes. |
format | Online Article Text |
id | pubmed-4585414 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-45854142015-09-29 Genome-wide association mapping of growth dynamics detects time-specific and general quantitative trait loci Bac-Molenaar, Johanna A. Vreugdenhil, Dick Granier, Christine Keurentjes, Joost J.B. J Exp Bot Research Paper Growth is a complex trait determined by the interplay between many genes, some of which play a role at a specific moment during development whereas others play a more general role. To identify the genetic basis of growth, natural variation in Arabidopsis rosette growth was followed in 324 accessions by a combination of top-view imaging, high-throughput image analysis, modelling of growth dynamics, and end-point fresh weight determination. Genome-wide association (GWA) mapping of the temporal growth data resulted in the detection of time-specific quantitative trait loci (QTLs), whereas mapping of model parameters resulted in another set of QTLs related to the whole growth curve. The positive correlation between projected leaf area (PLA) at different time points during the course of the experiment suggested the existence of general growth factors with a function in multiple developmental stages or with prolonged downstream effects. Many QTLs could not be identified when growth was evaluated only at a single time point. Eleven candidate genes were identified, which were annotated to be involved in the determination of cell number and size, seed germination, embryo development, developmental phase transition, or senescence. For eight of these, a mutant or overexpression phenotype related to growth has been reported, supporting the identification of true positives. In addition, the detection of QTLs without obvious candidate genes implies the annotation of novel functions for underlying genes. Oxford University Press 2015-09 2015-04-28 /pmc/articles/PMC4585414/ /pubmed/25922493 http://dx.doi.org/10.1093/jxb/erv176 Text en © The Author 2015. Published by Oxford University Press on behalf of the Society for Experimental Biology. http://creativecommons.org/licenses/by/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Bac-Molenaar, Johanna A. Vreugdenhil, Dick Granier, Christine Keurentjes, Joost J.B. Genome-wide association mapping of growth dynamics detects time-specific and general quantitative trait loci |
title | Genome-wide association mapping of growth dynamics detects time-specific and general quantitative trait loci |
title_full | Genome-wide association mapping of growth dynamics detects time-specific and general quantitative trait loci |
title_fullStr | Genome-wide association mapping of growth dynamics detects time-specific and general quantitative trait loci |
title_full_unstemmed | Genome-wide association mapping of growth dynamics detects time-specific and general quantitative trait loci |
title_short | Genome-wide association mapping of growth dynamics detects time-specific and general quantitative trait loci |
title_sort | genome-wide association mapping of growth dynamics detects time-specific and general quantitative trait loci |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4585414/ https://www.ncbi.nlm.nih.gov/pubmed/25922493 http://dx.doi.org/10.1093/jxb/erv176 |
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