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

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

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

2014
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Overview
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.