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Complex genetic architecture underlies maize tassel domestication

Maize (Zea mays) tassels underwent profound morphological changes during maize domestication and improvement. Although a number of genes affecting maize inflorescence development have been identified, the genetic basis of the morphological changes in maize tassels since domestication is not well und...

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Autores principales: Xu, Guanghui, Wang, Xufeng, Huang, Cheng, Xu, Dingyi, Li, Dan, Tian, Jinge, Chen, Qiuyue, Wang, Chenglong, Liang, Yameng, Wu, Yaoyao, Yang, Xiaohong, Tian, Feng
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/PMC5363343/
https://www.ncbi.nlm.nih.gov/pubmed/28067953
http://dx.doi.org/10.1111/nph.14400
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author Xu, Guanghui
Wang, Xufeng
Huang, Cheng
Xu, Dingyi
Li, Dan
Tian, Jinge
Chen, Qiuyue
Wang, Chenglong
Liang, Yameng
Wu, Yaoyao
Yang, Xiaohong
Tian, Feng
author_facet Xu, Guanghui
Wang, Xufeng
Huang, Cheng
Xu, Dingyi
Li, Dan
Tian, Jinge
Chen, Qiuyue
Wang, Chenglong
Liang, Yameng
Wu, Yaoyao
Yang, Xiaohong
Tian, Feng
author_sort Xu, Guanghui
collection PubMed
description Maize (Zea mays) tassels underwent profound morphological changes during maize domestication and improvement. Although a number of genes affecting maize inflorescence development have been identified, the genetic basis of the morphological changes in maize tassels since domestication is not well understood. Here, using a large population of 866 maize‐teosinte BC (2)S(3) recombinant inbred lines genotyped using 19 838 single nucleotide polymorphism (SNP) markers, we performed high‐resolution quantitative trait locus (QTL) mapping for five tassel morphological traits. We showed that the five tassel traits were associated with different genetic architecture features. Known genes for maize inflorescence development identified by mutagenesis were significantly enriched in the tassel trait QTLs, and many of these genes, including ramosa1 (ra1), barren inflorescence2 (bif2), unbranched2 (ub2), zea floricaula leafy2 (zfl2) and barren stalk fastigiate1 (baf1), showed evidence of selection. An in‐depth nucleotide diversity analysis at the bif2 locus identified strong selection signatures in the 5′‐regulatory region. We also found that several known flowering time genes co‐localized with tassel trait QTLs. A further association analysis indicated that the maize photoperiod gene ZmCCT was significantly associated with tassel size variation. Using near‐isogenic lines, we narrowed down a major‐effect QTL for tassel length, qTL9‐1, to a 513‐kb physical region. These results provide important insights into the genetic architecture that controls maize tassel evolution.
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spelling pubmed-53633432017-04-06 Complex genetic architecture underlies maize tassel domestication Xu, Guanghui Wang, Xufeng Huang, Cheng Xu, Dingyi Li, Dan Tian, Jinge Chen, Qiuyue Wang, Chenglong Liang, Yameng Wu, Yaoyao Yang, Xiaohong Tian, Feng New Phytol Research Maize (Zea mays) tassels underwent profound morphological changes during maize domestication and improvement. Although a number of genes affecting maize inflorescence development have been identified, the genetic basis of the morphological changes in maize tassels since domestication is not well understood. Here, using a large population of 866 maize‐teosinte BC (2)S(3) recombinant inbred lines genotyped using 19 838 single nucleotide polymorphism (SNP) markers, we performed high‐resolution quantitative trait locus (QTL) mapping for five tassel morphological traits. We showed that the five tassel traits were associated with different genetic architecture features. Known genes for maize inflorescence development identified by mutagenesis were significantly enriched in the tassel trait QTLs, and many of these genes, including ramosa1 (ra1), barren inflorescence2 (bif2), unbranched2 (ub2), zea floricaula leafy2 (zfl2) and barren stalk fastigiate1 (baf1), showed evidence of selection. An in‐depth nucleotide diversity analysis at the bif2 locus identified strong selection signatures in the 5′‐regulatory region. We also found that several known flowering time genes co‐localized with tassel trait QTLs. A further association analysis indicated that the maize photoperiod gene ZmCCT was significantly associated with tassel size variation. Using near‐isogenic lines, we narrowed down a major‐effect QTL for tassel length, qTL9‐1, to a 513‐kb physical region. These results provide important insights into the genetic architecture that controls maize tassel evolution. John Wiley and Sons Inc. 2017-01-09 2017-04 /pmc/articles/PMC5363343/ /pubmed/28067953 http://dx.doi.org/10.1111/nph.14400 Text en © 2017 The Authors. New Phytologist © 2017 New Phytologist Trust 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
Xu, Guanghui
Wang, Xufeng
Huang, Cheng
Xu, Dingyi
Li, Dan
Tian, Jinge
Chen, Qiuyue
Wang, Chenglong
Liang, Yameng
Wu, Yaoyao
Yang, Xiaohong
Tian, Feng
Complex genetic architecture underlies maize tassel domestication
title Complex genetic architecture underlies maize tassel domestication
title_full Complex genetic architecture underlies maize tassel domestication
title_fullStr Complex genetic architecture underlies maize tassel domestication
title_full_unstemmed Complex genetic architecture underlies maize tassel domestication
title_short Complex genetic architecture underlies maize tassel domestication
title_sort complex genetic architecture underlies maize tassel domestication
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5363343/
https://www.ncbi.nlm.nih.gov/pubmed/28067953
http://dx.doi.org/10.1111/nph.14400
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