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Segregation of a QTL cluster for home-cage activity using a new mapping method based on regression analysis of congenic mouse strains

Recent genetic studies have shown that genetic loci with significant effects in whole-genome quantitative trait loci (QTL) analyses were lost or weakened in congenic strains. Characterisation of the genetic basis of this attenuated QTL effect is important to our understanding of the genetic mechanis...

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Autores principales: Kato, S, Ishii, A, Nishi, A, Kuriki, S, Koide, T
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4220717/
https://www.ncbi.nlm.nih.gov/pubmed/24781804
http://dx.doi.org/10.1038/hdy.2014.42
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author Kato, S
Ishii, A
Nishi, A
Kuriki, S
Koide, T
author_facet Kato, S
Ishii, A
Nishi, A
Kuriki, S
Koide, T
author_sort Kato, S
collection PubMed
description Recent genetic studies have shown that genetic loci with significant effects in whole-genome quantitative trait loci (QTL) analyses were lost or weakened in congenic strains. Characterisation of the genetic basis of this attenuated QTL effect is important to our understanding of the genetic mechanisms of complex traits. We previously found that a consomic strain, B6-Chr6C(MSM), which carries chromosome 6 of a wild-derived strain MSM/Ms on the genetic background of C57BL/6J, exhibited lower home-cage activity than C57BL/6J. In the present study, we conducted a composite interval QTL analysis using the F2 mice derived from a cross between C57BL/6J and B6-Chr6C(MSM). We found one QTL peak that spans 17.6 Mbp of chromosome 6. A subconsomic strain that covers the entire QTL region also showed lower home-cage activity at the same level as the consomic strain. We developed 15 congenic strains, each of which carries a shorter MSM/Ms-derived chromosomal segment from the subconsomic strain. Given that the results of home-cage activity tests on the congenic strains cannot be explained by a simple single-gene model, we applied regression analysis to segregate the multiple genetic loci. The results revealed three loci (loci 1–3) that have the effect of reducing home-cage activity and one locus (locus 4) that increases activity. We also found that the combination of loci 3 and 4 cancels out the effects of the congenic strains, which indicates the existence of a genetic mechanism related to the loss of QTLs.
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spelling pubmed-42207172014-11-06 Segregation of a QTL cluster for home-cage activity using a new mapping method based on regression analysis of congenic mouse strains Kato, S Ishii, A Nishi, A Kuriki, S Koide, T Heredity (Edinb) Original Article Recent genetic studies have shown that genetic loci with significant effects in whole-genome quantitative trait loci (QTL) analyses were lost or weakened in congenic strains. Characterisation of the genetic basis of this attenuated QTL effect is important to our understanding of the genetic mechanisms of complex traits. We previously found that a consomic strain, B6-Chr6C(MSM), which carries chromosome 6 of a wild-derived strain MSM/Ms on the genetic background of C57BL/6J, exhibited lower home-cage activity than C57BL/6J. In the present study, we conducted a composite interval QTL analysis using the F2 mice derived from a cross between C57BL/6J and B6-Chr6C(MSM). We found one QTL peak that spans 17.6 Mbp of chromosome 6. A subconsomic strain that covers the entire QTL region also showed lower home-cage activity at the same level as the consomic strain. We developed 15 congenic strains, each of which carries a shorter MSM/Ms-derived chromosomal segment from the subconsomic strain. Given that the results of home-cage activity tests on the congenic strains cannot be explained by a simple single-gene model, we applied regression analysis to segregate the multiple genetic loci. The results revealed three loci (loci 1–3) that have the effect of reducing home-cage activity and one locus (locus 4) that increases activity. We also found that the combination of loci 3 and 4 cancels out the effects of the congenic strains, which indicates the existence of a genetic mechanism related to the loss of QTLs. Nature Publishing Group 2014-11 2014-04-30 /pmc/articles/PMC4220717/ /pubmed/24781804 http://dx.doi.org/10.1038/hdy.2014.42 Text en Copyright © 2014 The Genetics Society http://creativecommons.org/licenses/by-nc-sa/3.0/ This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. The images or other third party material in this article are included in the article's Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-sa/3.0/
spellingShingle Original Article
Kato, S
Ishii, A
Nishi, A
Kuriki, S
Koide, T
Segregation of a QTL cluster for home-cage activity using a new mapping method based on regression analysis of congenic mouse strains
title Segregation of a QTL cluster for home-cage activity using a new mapping method based on regression analysis of congenic mouse strains
title_full Segregation of a QTL cluster for home-cage activity using a new mapping method based on regression analysis of congenic mouse strains
title_fullStr Segregation of a QTL cluster for home-cage activity using a new mapping method based on regression analysis of congenic mouse strains
title_full_unstemmed Segregation of a QTL cluster for home-cage activity using a new mapping method based on regression analysis of congenic mouse strains
title_short Segregation of a QTL cluster for home-cage activity using a new mapping method based on regression analysis of congenic mouse strains
title_sort segregation of a qtl cluster for home-cage activity using a new mapping method based on regression analysis of congenic mouse strains
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4220717/
https://www.ncbi.nlm.nih.gov/pubmed/24781804
http://dx.doi.org/10.1038/hdy.2014.42
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