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Characterization of Linkage Disequilibrium and Population Structure in a Mungbean Diversity Panel
Mungbean [Vigna radiata (L.) R. Wilczek var. radiata] is an important grain legume globally, providing a high-quality plant protein source largely produced and consumed in South and East Asia. This study aimed to characterize a mungbean diversity panel consisting of 466 cultivated accessions and dem...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5770403/ https://www.ncbi.nlm.nih.gov/pubmed/29375590 http://dx.doi.org/10.3389/fpls.2017.02102 |
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author | Noble, Thomas J. Tao, Yongfu Mace, Emma S. Williams, Brett Jordan, David R. Douglas, Colin A. Mundree, Sagadevan G. |
author_facet | Noble, Thomas J. Tao, Yongfu Mace, Emma S. Williams, Brett Jordan, David R. Douglas, Colin A. Mundree, Sagadevan G. |
author_sort | Noble, Thomas J. |
collection | PubMed |
description | Mungbean [Vigna radiata (L.) R. Wilczek var. radiata] is an important grain legume globally, providing a high-quality plant protein source largely produced and consumed in South and East Asia. This study aimed to characterize a mungbean diversity panel consisting of 466 cultivated accessions and demonstrate its utility by conducting a pilot genome-wide association study of seed coat color. In addition 16 wild accessions were genotyped for comparison and in total over 22,000 polymorphic genome-wide SNPs were identified and used to analyze the genetic diversity, population structure, linkage disequilibrium (LD) of mungbean. Polymorphism was lower in the cultivated accessions in comparison to the wild accessions, with average polymorphism information content values 0.174, versus 0.305 in wild mungbean. LD decayed in ∼100 kb in cultivated lines, a distance higher than the linkage decay of ∼60 kb estimated in wild mungbean. Four distinct subgroups were identified within the cultivated lines, which broadly corresponded to geographic origin and seed characteristics. In a pilot genome-wide association mapping study of seed coat color, five genomic regions associated were identified, two of which were close to seed coat color genes in other species. This mungbean diversity panel constitutes a valuable resource for genetic dissection of important agronomical traits to accelerate mungbean breeding. |
format | Online Article Text |
id | pubmed-5770403 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-57704032018-01-26 Characterization of Linkage Disequilibrium and Population Structure in a Mungbean Diversity Panel Noble, Thomas J. Tao, Yongfu Mace, Emma S. Williams, Brett Jordan, David R. Douglas, Colin A. Mundree, Sagadevan G. Front Plant Sci Plant Science Mungbean [Vigna radiata (L.) R. Wilczek var. radiata] is an important grain legume globally, providing a high-quality plant protein source largely produced and consumed in South and East Asia. This study aimed to characterize a mungbean diversity panel consisting of 466 cultivated accessions and demonstrate its utility by conducting a pilot genome-wide association study of seed coat color. In addition 16 wild accessions were genotyped for comparison and in total over 22,000 polymorphic genome-wide SNPs were identified and used to analyze the genetic diversity, population structure, linkage disequilibrium (LD) of mungbean. Polymorphism was lower in the cultivated accessions in comparison to the wild accessions, with average polymorphism information content values 0.174, versus 0.305 in wild mungbean. LD decayed in ∼100 kb in cultivated lines, a distance higher than the linkage decay of ∼60 kb estimated in wild mungbean. Four distinct subgroups were identified within the cultivated lines, which broadly corresponded to geographic origin and seed characteristics. In a pilot genome-wide association mapping study of seed coat color, five genomic regions associated were identified, two of which were close to seed coat color genes in other species. This mungbean diversity panel constitutes a valuable resource for genetic dissection of important agronomical traits to accelerate mungbean breeding. Frontiers Media S.A. 2018-01-12 /pmc/articles/PMC5770403/ /pubmed/29375590 http://dx.doi.org/10.3389/fpls.2017.02102 Text en Copyright © 2018 Noble, Tao, Mace, Williams, Jordan, Douglas and Mundree. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Noble, Thomas J. Tao, Yongfu Mace, Emma S. Williams, Brett Jordan, David R. Douglas, Colin A. Mundree, Sagadevan G. Characterization of Linkage Disequilibrium and Population Structure in a Mungbean Diversity Panel |
title | Characterization of Linkage Disequilibrium and Population Structure in a Mungbean Diversity Panel |
title_full | Characterization of Linkage Disequilibrium and Population Structure in a Mungbean Diversity Panel |
title_fullStr | Characterization of Linkage Disequilibrium and Population Structure in a Mungbean Diversity Panel |
title_full_unstemmed | Characterization of Linkage Disequilibrium and Population Structure in a Mungbean Diversity Panel |
title_short | Characterization of Linkage Disequilibrium and Population Structure in a Mungbean Diversity Panel |
title_sort | characterization of linkage disequilibrium and population structure in a mungbean diversity panel |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5770403/ https://www.ncbi.nlm.nih.gov/pubmed/29375590 http://dx.doi.org/10.3389/fpls.2017.02102 |
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