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The genetic architecture of amino acids dissection by association and linkage analysis in maize

Amino acids are both constituents of proteins, providing the essential nutrition for humans and animals, and signalling molecules regulating the growth and development of plants. Most cultivars of maize are deficient in essential amino acids such as lysine and tryptophan. Here, we measured the level...

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Autores principales: Deng, Min, Li, Dongqin, Luo, Jingyun, Xiao, Yingjie, Liu, Haijun, Pan, Qingchun, Zhang, Xuehai, Jin, Minliang, Zhao, Mingchao, Yan, Jianbing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595712/
https://www.ncbi.nlm.nih.gov/pubmed/28218981
http://dx.doi.org/10.1111/pbi.12712
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author Deng, Min
Li, Dongqin
Luo, Jingyun
Xiao, Yingjie
Liu, Haijun
Pan, Qingchun
Zhang, Xuehai
Jin, Minliang
Zhao, Mingchao
Yan, Jianbing
author_facet Deng, Min
Li, Dongqin
Luo, Jingyun
Xiao, Yingjie
Liu, Haijun
Pan, Qingchun
Zhang, Xuehai
Jin, Minliang
Zhao, Mingchao
Yan, Jianbing
author_sort Deng, Min
collection PubMed
description Amino acids are both constituents of proteins, providing the essential nutrition for humans and animals, and signalling molecules regulating the growth and development of plants. Most cultivars of maize are deficient in essential amino acids such as lysine and tryptophan. Here, we measured the levels of 17 different total amino acids, and created 48 derived traits in mature kernels from a maize diversity inbred collection and three recombinant inbred line (RIL) populations. By GWAS, 247 and 281 significant loci were identified in two different environments, 5.1 and 4.4 loci for each trait, explaining 7.44% and 7.90% phenotypic variation for each locus in average, respectively. By linkage mapping, 89, 150 and 165 QTLs were identified in B73/By804, Kui3/B77 and Zong3/Yu87‐1 RIL populations, 2.0, 2.7 and 2.8 QTLs for each trait, explaining 13.6%, 16.4% and 21.4% phenotypic variation for each QTL in average, respectively. It implies that the genetic architecture of amino acids is relative simple and controlled by limited loci. About 43.2% of the loci identified by GWAS were verified by expression QTL, and 17 loci overlapped with mapped QTLs in the three RIL populations. GRMZM2G015534, GRMZM2G143008 and one QTL were further validated using molecular approaches. The amino acid biosynthetic and catabolic pathways were reconstructed on the basis of candidate genes proposed in this study. Our results provide insights into the genetic basis of amino acid biosynthesis in maize kernels and may facilitate marker‐based breeding for quality protein maize.
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spelling pubmed-55957122017-09-26 The genetic architecture of amino acids dissection by association and linkage analysis in maize Deng, Min Li, Dongqin Luo, Jingyun Xiao, Yingjie Liu, Haijun Pan, Qingchun Zhang, Xuehai Jin, Minliang Zhao, Mingchao Yan, Jianbing Plant Biotechnol J Research Articles Amino acids are both constituents of proteins, providing the essential nutrition for humans and animals, and signalling molecules regulating the growth and development of plants. Most cultivars of maize are deficient in essential amino acids such as lysine and tryptophan. Here, we measured the levels of 17 different total amino acids, and created 48 derived traits in mature kernels from a maize diversity inbred collection and three recombinant inbred line (RIL) populations. By GWAS, 247 and 281 significant loci were identified in two different environments, 5.1 and 4.4 loci for each trait, explaining 7.44% and 7.90% phenotypic variation for each locus in average, respectively. By linkage mapping, 89, 150 and 165 QTLs were identified in B73/By804, Kui3/B77 and Zong3/Yu87‐1 RIL populations, 2.0, 2.7 and 2.8 QTLs for each trait, explaining 13.6%, 16.4% and 21.4% phenotypic variation for each QTL in average, respectively. It implies that the genetic architecture of amino acids is relative simple and controlled by limited loci. About 43.2% of the loci identified by GWAS were verified by expression QTL, and 17 loci overlapped with mapped QTLs in the three RIL populations. GRMZM2G015534, GRMZM2G143008 and one QTL were further validated using molecular approaches. The amino acid biosynthetic and catabolic pathways were reconstructed on the basis of candidate genes proposed in this study. Our results provide insights into the genetic basis of amino acid biosynthesis in maize kernels and may facilitate marker‐based breeding for quality protein maize. John Wiley and Sons Inc. 2017-04-05 2017-10 /pmc/articles/PMC5595712/ /pubmed/28218981 http://dx.doi.org/10.1111/pbi.12712 Text en © 2017 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 Creative Commons Attribution (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
Deng, Min
Li, Dongqin
Luo, Jingyun
Xiao, Yingjie
Liu, Haijun
Pan, Qingchun
Zhang, Xuehai
Jin, Minliang
Zhao, Mingchao
Yan, Jianbing
The genetic architecture of amino acids dissection by association and linkage analysis in maize
title The genetic architecture of amino acids dissection by association and linkage analysis in maize
title_full The genetic architecture of amino acids dissection by association and linkage analysis in maize
title_fullStr The genetic architecture of amino acids dissection by association and linkage analysis in maize
title_full_unstemmed The genetic architecture of amino acids dissection by association and linkage analysis in maize
title_short The genetic architecture of amino acids dissection by association and linkage analysis in maize
title_sort genetic architecture of amino acids dissection by association and linkage analysis in maize
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595712/
https://www.ncbi.nlm.nih.gov/pubmed/28218981
http://dx.doi.org/10.1111/pbi.12712
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