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Time‐specific and pleiotropic quantitative trait loci coordinately modulate stem growth in Populus

In perennial woody plants, the coordinated increase of stem height and diameter during juvenile growth improves competitiveness (i.e. access to light); however, the factors underlying variation in stem growth remain unknown in trees. Here, we used linkage‐linkage disequilibrium (linkage‐LD) mapping...

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Autores principales: Du, Qingzhang, Yang, Xiaohui, Xie, Jianbo, Quan, Mingyang, Xiao, Liang, Lu, Wenjie, Tian, Jiaxing, Gong, Chenrui, Chen, Jinhui, Li, Bailian, Zhang, Deqiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381792/
https://www.ncbi.nlm.nih.gov/pubmed/30133117
http://dx.doi.org/10.1111/pbi.13002
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author Du, Qingzhang
Yang, Xiaohui
Xie, Jianbo
Quan, Mingyang
Xiao, Liang
Lu, Wenjie
Tian, Jiaxing
Gong, Chenrui
Chen, Jinhui
Li, Bailian
Zhang, Deqiang
author_facet Du, Qingzhang
Yang, Xiaohui
Xie, Jianbo
Quan, Mingyang
Xiao, Liang
Lu, Wenjie
Tian, Jiaxing
Gong, Chenrui
Chen, Jinhui
Li, Bailian
Zhang, Deqiang
author_sort Du, Qingzhang
collection PubMed
description In perennial woody plants, the coordinated increase of stem height and diameter during juvenile growth improves competitiveness (i.e. access to light); however, the factors underlying variation in stem growth remain unknown in trees. Here, we used linkage‐linkage disequilibrium (linkage‐LD) mapping to decipher the genetic architecture underlying three growth traits during juvenile stem growth. We used two Populus populations: a linkage mapping population comprising a full‐sib family of 1,200 progeny and an association mapping panel comprising 435 unrelated individuals from nearly the entire natural range of Populus tomentosa. We mapped 311 quantitative trait loci (QTL) for three growth traits at 12 timepoints to 42 regions in 17 linkage groups. Of these, 28 regions encompassing 233 QTL were annotated as 27 segmental homology regions (SHRs). Using SNPs identified by whole‐genome re‐sequencing of the 435‐member association mapping panel, we identified significant SNPs (P ≤ 9.4 × 10(−7)) within 27 SHRs that affect stem growth at nine timepoints with diverse additive and dominance patterns, and these SNPs exhibited complex allelic epistasis over the juvenile growth period. Nineteen genes linked to potential causative alleles that have time‐specific or pleiotropic effects, and mostly overlapped with significant signatures of selection within SHRs between climatic regions represented by the association mapping panel. Five genes with potential time‐specific effects showed species‐specific temporal expression profiles during the juvenile stages of stem growth in five representative Populus species. Our observations revealed the importance of considering temporal genetic basis of complex traits, which will facilitate the molecular design of tree ideotypes.
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spelling pubmed-63817922019-03-01 Time‐specific and pleiotropic quantitative trait loci coordinately modulate stem growth in Populus Du, Qingzhang Yang, Xiaohui Xie, Jianbo Quan, Mingyang Xiao, Liang Lu, Wenjie Tian, Jiaxing Gong, Chenrui Chen, Jinhui Li, Bailian Zhang, Deqiang Plant Biotechnol J Research Articles In perennial woody plants, the coordinated increase of stem height and diameter during juvenile growth improves competitiveness (i.e. access to light); however, the factors underlying variation in stem growth remain unknown in trees. Here, we used linkage‐linkage disequilibrium (linkage‐LD) mapping to decipher the genetic architecture underlying three growth traits during juvenile stem growth. We used two Populus populations: a linkage mapping population comprising a full‐sib family of 1,200 progeny and an association mapping panel comprising 435 unrelated individuals from nearly the entire natural range of Populus tomentosa. We mapped 311 quantitative trait loci (QTL) for three growth traits at 12 timepoints to 42 regions in 17 linkage groups. Of these, 28 regions encompassing 233 QTL were annotated as 27 segmental homology regions (SHRs). Using SNPs identified by whole‐genome re‐sequencing of the 435‐member association mapping panel, we identified significant SNPs (P ≤ 9.4 × 10(−7)) within 27 SHRs that affect stem growth at nine timepoints with diverse additive and dominance patterns, and these SNPs exhibited complex allelic epistasis over the juvenile growth period. Nineteen genes linked to potential causative alleles that have time‐specific or pleiotropic effects, and mostly overlapped with significant signatures of selection within SHRs between climatic regions represented by the association mapping panel. Five genes with potential time‐specific effects showed species‐specific temporal expression profiles during the juvenile stages of stem growth in five representative Populus species. Our observations revealed the importance of considering temporal genetic basis of complex traits, which will facilitate the molecular design of tree ideotypes. John Wiley and Sons Inc. 2018-09-17 2019-03 /pmc/articles/PMC6381792/ /pubmed/30133117 http://dx.doi.org/10.1111/pbi.13002 Text en © 2018 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Du, Qingzhang
Yang, Xiaohui
Xie, Jianbo
Quan, Mingyang
Xiao, Liang
Lu, Wenjie
Tian, Jiaxing
Gong, Chenrui
Chen, Jinhui
Li, Bailian
Zhang, Deqiang
Time‐specific and pleiotropic quantitative trait loci coordinately modulate stem growth in Populus
title Time‐specific and pleiotropic quantitative trait loci coordinately modulate stem growth in Populus
title_full Time‐specific and pleiotropic quantitative trait loci coordinately modulate stem growth in Populus
title_fullStr Time‐specific and pleiotropic quantitative trait loci coordinately modulate stem growth in Populus
title_full_unstemmed Time‐specific and pleiotropic quantitative trait loci coordinately modulate stem growth in Populus
title_short Time‐specific and pleiotropic quantitative trait loci coordinately modulate stem growth in Populus
title_sort time‐specific and pleiotropic quantitative trait loci coordinately modulate stem growth in populus
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6381792/
https://www.ncbi.nlm.nih.gov/pubmed/30133117
http://dx.doi.org/10.1111/pbi.13002
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