The objective of this proposal is to identify genetic factors in a mouse model that predispose individuals to type 2 diabetes. The project will focus on defining the genetics of diet-induced insulin resistance and hyperglycemia which are characteristic of the C57BL/6J (BL/6) mouse. The segregation of insulin resistance, hyperinsulinemia, hyperglycemia and obesity on a high fat, high simple carbohydrate diet will be analyzed in crosses between diabetes susceptible C57BL/6J and resistant A/J mice utilizing backcrosses, recombinant inbred (RI) and recombinant congenics (RC) of these strains. We will examine whether the loci which result in each manifestation of this disease segregate traits on the BL/6 genome will be determined by their strain distribution pattern in at least 14 BXA and 19 AXB RI strains by comparison with previously typed genetic markers and additional markers to be characterized. Restriction fragment length variants (RFLV) will be determined for both disease candidate loci and evenly spaced genetic markers throughout genome in order to enhance the probability of identifying a genetic locus. Similarly, evenly spaced RFLV markers will be typed in 25 RC strains. Finally, DNA from appropriate backcross mice will be analyzed to confirm the identification of candidate genetic loci. These studies will determine the feasibility of reverse genetic approaches to cloning of """"""""diabetagenic"""""""" gene(s) in the mouse and identity possible candidate loci for human genetic linkage studies.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK042923-02
Application #
3244135
Study Section
Metabolism Study Section (MET)
Project Start
1991-07-01
Project End
1994-06-30
Budget Start
1992-07-01
Budget End
1993-06-30
Support Year
2
Fiscal Year
1992
Total Cost
Indirect Cost
Name
Duke University
Department
Type
Schools of Medicine
DUNS #
071723621
City
Durham
State
NC
Country
United States
Zip Code
27705
Surwit, R S; Williams, P G (1996) Animal models provide insight into psychosomatic factors in diabetes. Psychosom Med 58:582-9
Brownlow, B S; Petro, A; Feinglos, M N et al. (1996) The role of motor activity in diet-induced obesity in C57BL/6J mice. Physiol Behav 60:37-41
Gettys, T W; Ramkumar, V; Surwit, R S et al. (1995) Tissue-specific alterations in G protein expression in genetic versus diet-induced models of non-insulin-dependent diabetes mellitus in the mouse. Metabolism 44:771-8
Lee, S K; Opara, E C; Surwit, R S et al. (1995) Defective glucose-stimulated insulin release from perifused islets of C57BL/6J mice. Pancreas 11:206-11
Wencel, H E; Smothers, C; Opara, E C et al. (1995) Impaired second phase insulin response of diabetes-prone C57BL/6J mouse islets. Physiol Behav 57:1215-20
Seldin, M F; Mott, D; Bhat, D et al. (1994) Glycogen synthase: a putative locus for diet-induced hyperglycemia. J Clin Invest 94:269-76
Rebuffe-Scrive, M; Surwit, R; Feinglos, M et al. (1993) Regional fat distribution and metabolism in a new mouse model (C57BL/6J) of non-insulin-dependent diabetes mellitus. Metabolism 42:1405-9
Seldin, M F; Hunter, K; Watson, M L (1993) Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 1. Mamm Genome 4 Spec No:S10-30
Surwit, R S; Schneider, M S (1993) Role of stress in the etiology and treatment of diabetes mellitus. Psychosom Med 55:380-93
Seldin, M F; Prins, J B; Rodrigues, N R et al. (1993) Encyclopedia of the mouse genome III. October 1993. Mouse chromosome 3. Mamm Genome 4 Spec No:S47-57

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