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Footprints of Selection Derived From Temporal Heterozygosity Patterns in a Barley Nested Association Mapping Population
Nowadays, genetic diversity more than ever represents a key driver of adaptation to climate challenges like drought, heat, and salinity. Therefore, there is a need to replenish the limited elite gene pools with favorable exotic alleles from the wild progenitors of our crops. Nested association mappi...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551860/ https://www.ncbi.nlm.nih.gov/pubmed/34721490 http://dx.doi.org/10.3389/fpls.2021.764537 |
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author | Maurer, Andreas Pillen, Klaus |
author_facet | Maurer, Andreas Pillen, Klaus |
author_sort | Maurer, Andreas |
collection | PubMed |
description | Nowadays, genetic diversity more than ever represents a key driver of adaptation to climate challenges like drought, heat, and salinity. Therefore, there is a need to replenish the limited elite gene pools with favorable exotic alleles from the wild progenitors of our crops. Nested association mapping (NAM) populations represent one step toward exotic allele evaluation and enrichment of the elite gene pool. We investigated an adaptive selection strategy in the wild barley NAM population HEB-25 based on temporal genomic data by studying the fate of 214,979 SNP loci initially heterozygous in individual BC(1)S(3) lines after five cycles of selfing and field propagation. We identified several loci exposed to adaptive selection in HEB-25. In total, 48.7% (104,725 SNPs) of initially heterozygous SNP calls in HEB-25 were fixed in BC(1)S(3:8) generation, either toward the wild allele (19.9%) or the cultivated allele (28.8%). Most fixed SNP loci turned out to represent gene loci involved in domestication and flowering time as well as plant height, for example, btr1/btr2, thresh-1, Ppd-H1, and sdw1. Interestingly, also unknown loci were found where the exotic allele was fixed, hinting at potentially useful exotic alleles for plant breeding. |
format | Online Article Text |
id | pubmed-8551860 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-85518602021-10-29 Footprints of Selection Derived From Temporal Heterozygosity Patterns in a Barley Nested Association Mapping Population Maurer, Andreas Pillen, Klaus Front Plant Sci Plant Science Nowadays, genetic diversity more than ever represents a key driver of adaptation to climate challenges like drought, heat, and salinity. Therefore, there is a need to replenish the limited elite gene pools with favorable exotic alleles from the wild progenitors of our crops. Nested association mapping (NAM) populations represent one step toward exotic allele evaluation and enrichment of the elite gene pool. We investigated an adaptive selection strategy in the wild barley NAM population HEB-25 based on temporal genomic data by studying the fate of 214,979 SNP loci initially heterozygous in individual BC(1)S(3) lines after five cycles of selfing and field propagation. We identified several loci exposed to adaptive selection in HEB-25. In total, 48.7% (104,725 SNPs) of initially heterozygous SNP calls in HEB-25 were fixed in BC(1)S(3:8) generation, either toward the wild allele (19.9%) or the cultivated allele (28.8%). Most fixed SNP loci turned out to represent gene loci involved in domestication and flowering time as well as plant height, for example, btr1/btr2, thresh-1, Ppd-H1, and sdw1. Interestingly, also unknown loci were found where the exotic allele was fixed, hinting at potentially useful exotic alleles for plant breeding. Frontiers Media S.A. 2021-10-14 /pmc/articles/PMC8551860/ /pubmed/34721490 http://dx.doi.org/10.3389/fpls.2021.764537 Text en Copyright © 2021 Maurer and Pillen. https://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) and the copyright owner(s) 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 Maurer, Andreas Pillen, Klaus Footprints of Selection Derived From Temporal Heterozygosity Patterns in a Barley Nested Association Mapping Population |
title | Footprints of Selection Derived From Temporal Heterozygosity Patterns in a Barley Nested Association Mapping Population |
title_full | Footprints of Selection Derived From Temporal Heterozygosity Patterns in a Barley Nested Association Mapping Population |
title_fullStr | Footprints of Selection Derived From Temporal Heterozygosity Patterns in a Barley Nested Association Mapping Population |
title_full_unstemmed | Footprints of Selection Derived From Temporal Heterozygosity Patterns in a Barley Nested Association Mapping Population |
title_short | Footprints of Selection Derived From Temporal Heterozygosity Patterns in a Barley Nested Association Mapping Population |
title_sort | footprints of selection derived from temporal heterozygosity patterns in a barley nested association mapping population |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8551860/ https://www.ncbi.nlm.nih.gov/pubmed/34721490 http://dx.doi.org/10.3389/fpls.2021.764537 |
work_keys_str_mv | AT maurerandreas footprintsofselectionderivedfromtemporalheterozygositypatternsinabarleynestedassociationmappingpopulation AT pillenklaus footprintsofselectionderivedfromtemporalheterozygositypatternsinabarleynestedassociationmappingpopulation |