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Genome-wide prediction methods for detecting genetic effects of donor chromosome segments in introgression populations

BACKGROUND: Introgression populations are used to make the genetic variation of unadapted germplasm or wild relatives of crops available for plant breeding. They consist of introgression lines that carry small chromosome segments from an exotic donor in the genetic background of an elite line. The g...

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Autores principales: Falke, Karen Christin, Mahone, Gregory S, Bauer, Eva, Haseneyer, Grit, Miedaner, Thomas, Breuer, Frank, Frisch, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4169839/
https://www.ncbi.nlm.nih.gov/pubmed/25213628
http://dx.doi.org/10.1186/1471-2164-15-782
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author Falke, Karen Christin
Mahone, Gregory S
Bauer, Eva
Haseneyer, Grit
Miedaner, Thomas
Breuer, Frank
Frisch, Matthias
author_facet Falke, Karen Christin
Mahone, Gregory S
Bauer, Eva
Haseneyer, Grit
Miedaner, Thomas
Breuer, Frank
Frisch, Matthias
author_sort Falke, Karen Christin
collection PubMed
description BACKGROUND: Introgression populations are used to make the genetic variation of unadapted germplasm or wild relatives of crops available for plant breeding. They consist of introgression lines that carry small chromosome segments from an exotic donor in the genetic background of an elite line. The goal of our study was to investigate the detection of favorable donor chromosome segments in introgression lines with statistical methods developed for genome-wide prediction. RESULTS: Computer simulations showed that genome-wide prediction employing heteroscedastic marker variances had a greater power and a lower false positive rate compared with homoscedastic marker variances when the phenotypic difference between the donor and recipient lines was controlled by few genes. The simulations helped to interpret the analyses of glycosinolate and linolenic acid content in a rapeseed introgression population and plant height in a rye introgression population. These analyses support the superiority of genome-wide prediction approaches that use heteroscedastic marker variances. CONCLUSIONS: We conclude that genome-wide prediction methods in combination with permutation tests can be employed for analysis of introgression populations. They are particularly useful when introgression lines carry several donor segments or when the donor segments of different introgression lines are overlapping.
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spelling pubmed-41698392014-09-22 Genome-wide prediction methods for detecting genetic effects of donor chromosome segments in introgression populations Falke, Karen Christin Mahone, Gregory S Bauer, Eva Haseneyer, Grit Miedaner, Thomas Breuer, Frank Frisch, Matthias BMC Genomics Research Article BACKGROUND: Introgression populations are used to make the genetic variation of unadapted germplasm or wild relatives of crops available for plant breeding. They consist of introgression lines that carry small chromosome segments from an exotic donor in the genetic background of an elite line. The goal of our study was to investigate the detection of favorable donor chromosome segments in introgression lines with statistical methods developed for genome-wide prediction. RESULTS: Computer simulations showed that genome-wide prediction employing heteroscedastic marker variances had a greater power and a lower false positive rate compared with homoscedastic marker variances when the phenotypic difference between the donor and recipient lines was controlled by few genes. The simulations helped to interpret the analyses of glycosinolate and linolenic acid content in a rapeseed introgression population and plant height in a rye introgression population. These analyses support the superiority of genome-wide prediction approaches that use heteroscedastic marker variances. CONCLUSIONS: We conclude that genome-wide prediction methods in combination with permutation tests can be employed for analysis of introgression populations. They are particularly useful when introgression lines carry several donor segments or when the donor segments of different introgression lines are overlapping. BioMed Central 2014-09-11 /pmc/articles/PMC4169839/ /pubmed/25213628 http://dx.doi.org/10.1186/1471-2164-15-782 Text en © Falke et al.; licensee BioMed Central Ltd. 2014 This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Falke, Karen Christin
Mahone, Gregory S
Bauer, Eva
Haseneyer, Grit
Miedaner, Thomas
Breuer, Frank
Frisch, Matthias
Genome-wide prediction methods for detecting genetic effects of donor chromosome segments in introgression populations
title Genome-wide prediction methods for detecting genetic effects of donor chromosome segments in introgression populations
title_full Genome-wide prediction methods for detecting genetic effects of donor chromosome segments in introgression populations
title_fullStr Genome-wide prediction methods for detecting genetic effects of donor chromosome segments in introgression populations
title_full_unstemmed Genome-wide prediction methods for detecting genetic effects of donor chromosome segments in introgression populations
title_short Genome-wide prediction methods for detecting genetic effects of donor chromosome segments in introgression populations
title_sort genome-wide prediction methods for detecting genetic effects of donor chromosome segments in introgression populations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4169839/
https://www.ncbi.nlm.nih.gov/pubmed/25213628
http://dx.doi.org/10.1186/1471-2164-15-782
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