Genetic factors are important in determining the risk for development of obesity as are environmental factors such as the percentage of fat in the diet. The long range goal is to characterize the genetic basis for the predisposition to obesity when challenged with a high-fat diet. Dr. West used an intercross between two strains, one susceptible to dietary fat induced obesity and one resistant, and identified six loci which have a significant effect on the susceptibility to dietary fat. The original Aims were to 1) complete a linkage map of the loci controlling differential sensitivity to dietary obesity in the AKR/J x SWR/J mouse model; 2) to evaluate the role of specific genetic loci linked to dietary obesity in the AKR/J x SWR/J model in several other genetic models of dietary obesity; 3) to develop congenic strains for four of the locus; and 4) to evaluate the role of specific candidate genes at these loci. The applicant has made excellent progress, completing the genotyping on the primary cross with the identification of 6-7 loci, constructing a number of congenics to the N5 generation, and testing several candidate genes. The current proposal is identify the gene underlying two of the loci. The first Specific Aim is to use the strategy of fine mapping and the characterization of expressed sequences in a small chromosomal region in order to identify the gene on proximal chromosome 15 of the mouse having a major effect on body fat. A candidate gene in the chromosome 12 QTL is Mod1r, a transcription factor which affects transcription of the structural gene for malic enzyme involved in carbohydrate and fat metabolism.
Specific Aim 2 will determine if AKR/J and SWR/J mice carry different alleles at the Mod1r regulatory locus and to fine map the Mod1r locus.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
2R01DK045895-04
Application #
2398851
Study Section
Nutrition Study Section (NTN)
Project Start
1994-09-15
Project End
2001-08-31
Budget Start
1997-09-01
Budget End
1998-08-31
Support Year
4
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Lsu Pennington Biomedical Research Center
Department
Type
Organized Research Units
DUNS #
City
Baton Rouge
State
LA
Country
United States
Zip Code
70808
Dhar, Madhu; Hauser, Loren; Johnson, Dabney (2002) An aminophospholipid translocase associated with body fat and type 2 diabetes phenotypes. Obes Res 10:695-702
Smith, B K; Volaufova, J; West, D B (2001) Increased flavor preference and lick activity for sucrose and corn oil in SWR/J vs. AKR/J mice. Am J Physiol Regul Integr Comp Physiol 281:R596-606
West, D B; Iakougova, O; Olsson, C et al. (2000) Mouse genetics/genomics: an effective approach for drug target discovery and validation. Med Res Rev 20:216-30
Smith, B K; Andrews, P K; West, D B (2000) Macronutrient diet selection in thirteen mouse strains. Am J Physiol Regul Integr Comp Physiol 278:R797-805
Dhar, M; Webb, L S; Smith, L et al. (2000) A novel ATPase on mouse chromosome 7 is a candidate gene for increased body fat. Physiol Genomics 4:93-100
Smith, B K; Andrews, P K; York, D A et al. (1999) Divergence in proportional fat intake in AKR/J and SWR/J mice endures across diet paradigms. Am J Physiol 277:R776-85
York, B; Truett, A A; Monteiro, M P et al. (1999) Gene-environment interaction: a significant diet-dependent obesity locus demonstrated in a congenic segment on mouse chromosome 7. Mamm Genome 10:457-62
West, D B; York, B (1998) Dietary fat, genetic predisposition, and obesity: lessons from animal models. Am J Clin Nutr 67:505S-512S
Smith, B K; West, D B; York, D A (1997) Carbohydrate versus fat intake: differing patterns of macronutrient selection in two inbred mouse strains. Am J Physiol 272:R357-62
York, B; Lei, K; West, D B (1997) Inherited non-autosomal effects on body fat in F2 mice derived from an AKR/J x SWR/J cross. Mamm Genome 8:726-30

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