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Combined detection and introgression of QTL in outbred populations

BACKGROUND: Detecting a QTL is only the first step in genetic improvement programs. When a QTL with desirable characteristics is found, e.g. in a wild or unimproved population, it may be interesting to introgress the detected QTL into the commercial population. One approach to shorten the time neede...

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Autores principales: Yazdi, M Hossein, Sonesson, Anna K, Woolliams, John A, Meuwissen, Theodorus HE
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2900242/
https://www.ncbi.nlm.nih.gov/pubmed/20525260
http://dx.doi.org/10.1186/1297-9686-42-16
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author Yazdi, M Hossein
Sonesson, Anna K
Woolliams, John A
Meuwissen, Theodorus HE
author_facet Yazdi, M Hossein
Sonesson, Anna K
Woolliams, John A
Meuwissen, Theodorus HE
author_sort Yazdi, M Hossein
collection PubMed
description BACKGROUND: Detecting a QTL is only the first step in genetic improvement programs. When a QTL with desirable characteristics is found, e.g. in a wild or unimproved population, it may be interesting to introgress the detected QTL into the commercial population. One approach to shorten the time needed for introgression is to combine both QTL identification and introgression, into a single step. This combines the strengths of fine mapping and backcrossing and paves the way for introgression of desirable but unknown QTL into recipient animal and plant lines. METHODS: The method consisting in combining QTL mapping and gene introgression has been extended from inbred to outbred populations in which QTL allele frequencies vary both in recipient and donor lines in different scenarios and for which polygenic effects are included in order to model background genes. The effectiveness of the combined QTL detection and introgression procedure was evaluated by simulation through four backcross generations. RESULTS: The allele substitution effect is underestimated when the favourable QTL allele is not fixed in the donor line. This underestimation is proportional to the frequency differences of the favourable QTL allele between the lines. In most scenarios, the estimates of the QTL location are unbiased and accurate. The retained donor chromosome segment and linkage drag are similar to expected values from other published studies. CONCLUSIONS: In general, our results show that it is possible to combine QTL detection and introgression even in outbred species. Separating QTL mapping and introgression processes is often thought to be longer and more costly. However, using a combined process saves at least one generation. With respect to the linkage drag and obligatory drag, the results of the combined detection and introgression scheme are very similar to those of traditional introgression schemes.
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spelling pubmed-29002422010-07-09 Combined detection and introgression of QTL in outbred populations Yazdi, M Hossein Sonesson, Anna K Woolliams, John A Meuwissen, Theodorus HE Genet Sel Evol Research BACKGROUND: Detecting a QTL is only the first step in genetic improvement programs. When a QTL with desirable characteristics is found, e.g. in a wild or unimproved population, it may be interesting to introgress the detected QTL into the commercial population. One approach to shorten the time needed for introgression is to combine both QTL identification and introgression, into a single step. This combines the strengths of fine mapping and backcrossing and paves the way for introgression of desirable but unknown QTL into recipient animal and plant lines. METHODS: The method consisting in combining QTL mapping and gene introgression has been extended from inbred to outbred populations in which QTL allele frequencies vary both in recipient and donor lines in different scenarios and for which polygenic effects are included in order to model background genes. The effectiveness of the combined QTL detection and introgression procedure was evaluated by simulation through four backcross generations. RESULTS: The allele substitution effect is underestimated when the favourable QTL allele is not fixed in the donor line. This underestimation is proportional to the frequency differences of the favourable QTL allele between the lines. In most scenarios, the estimates of the QTL location are unbiased and accurate. The retained donor chromosome segment and linkage drag are similar to expected values from other published studies. CONCLUSIONS: In general, our results show that it is possible to combine QTL detection and introgression even in outbred species. Separating QTL mapping and introgression processes is often thought to be longer and more costly. However, using a combined process saves at least one generation. With respect to the linkage drag and obligatory drag, the results of the combined detection and introgression scheme are very similar to those of traditional introgression schemes. BioMed Central 2010-06-03 /pmc/articles/PMC2900242/ /pubmed/20525260 http://dx.doi.org/10.1186/1297-9686-42-16 Text en Copyright ©2010 Yazdi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 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 cited.
spellingShingle Research
Yazdi, M Hossein
Sonesson, Anna K
Woolliams, John A
Meuwissen, Theodorus HE
Combined detection and introgression of QTL in outbred populations
title Combined detection and introgression of QTL in outbred populations
title_full Combined detection and introgression of QTL in outbred populations
title_fullStr Combined detection and introgression of QTL in outbred populations
title_full_unstemmed Combined detection and introgression of QTL in outbred populations
title_short Combined detection and introgression of QTL in outbred populations
title_sort combined detection and introgression of qtl in outbred populations
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2900242/
https://www.ncbi.nlm.nih.gov/pubmed/20525260
http://dx.doi.org/10.1186/1297-9686-42-16
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