Quantitative trait loci for impaired glucose tolerance in nondiabetic SM/J and A/J mice

1 Department of Applied Molecular Bioscience, Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, Japan 2 Division of Experimental Animals, Center for Promotion of Medical Research and Education, Graduate School of Medicine, Nagoya University, Nagoya, Japan The SMXA-5 recombinant...

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Veröffentlicht in:Physiological genomics 2008-09, Vol.35 (1), p.65-74
Hauptverfasser: Hada, Natsuko, Kobayashi, Misato, Fujiyoshi, Masato, Ishikawa, Akira, Kuga, Masako, Nishimura, Masahiko, Ebihara, Shizufumi, Ohno, Tamio, Horio, Fumihiko
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Sprache:eng
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Zusammenfassung:1 Department of Applied Molecular Bioscience, Graduate School of Bioagricultural Sciences, Nagoya University, Nagoya, Japan 2 Division of Experimental Animals, Center for Promotion of Medical Research and Education, Graduate School of Medicine, Nagoya University, Nagoya, Japan The SMXA-5 recombinant inbred strain, which was established from nondiabetic parental SM/J and A/J mice, develops diabetic phenotypes such as impaired glucose tolerance. The combination of diabetogenic genes in the SM/J and A/J genomes impairs glucose tolerance in SMXA-5 mice. Using (SM/J x SMXA-5)F2 mice fed a high-fat diet, we previously detected a diabetogenic locus, T2dm2sa , on chromosome (Chr) 2. The A/J allele at this locus is diabetogenic. The SM.A- T2dm2sa congenic mouse, in which the Chr 2 region of A/J including T2dm2sa was introgressed into SM/J, showed obviously impaired glucose tolerance. These results indicate that SM.A- T2dm2sa mice develop diabetogenic traits due to T2dm2sa with the A/J allele and unknown diabetogenic loci with the SM/J allele. The aim of this study was to dissect these unknown loci, using quantitative trait locus (QTL) analysis in the (A/J x SM.A- T2dm2sa ) F2 intercross fed a high-fat diet. The results revealed a highly significant QTL, T2dm4sa , for glucose tolerance on Chr 6 and a significant QTL, T2dm5sa , for glucose tolerance on Chr 11. These loci with the SM/J allele were diabetogenic. The diabetogenic effect of T2dm4sa or T2dm5sa was verified by the impairment of glucose tolerance in the A/J-6 SM or A/J-11 SM consomic strain, in which Chr 6 or Chr 11 of SM/J is introgressed into A/J, respectively. These results demonstrate that diabetogenic loci exist in the genomes of nondiabetic A/J and SM/J mice and suggest that T2dm2sa with the A/J allele and T2dm4sa and/or T2dm5sa with the SM/J allele elicit impaired glucose tolerance in SM.A- T2dm2sa mice. recombinant inbred mouse; type 2 diabetes; consomic; mouse chromosome 11; chromosome 6
ISSN:1094-8341
1531-2267
DOI:10.1152/physiolgenomics.00027.2008