| Project/Area Number |
11480249
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| Research Category |
Grant-in-Aid for Scientific Research (B)
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| Allocation Type | Single-year Grants |
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| Section | 一般 |
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| Research Field |
Laboratory animal science
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| Research Institution | The University of Tokushima |
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Principal Investigator |
MATSUMOTO Kozo The University of Tokushima, School of Medicine, Associate Professor, 医学部, 助教授 (00002246)
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| Co-Investigator(Kenkyū-buntansha) |
KOSE Hiroyuki The University of Tokushima, School of Medicine, Research Associate, 医学部, 助手 (90314856)
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| Project Period (FY) |
1999 – 2001
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| Project Status |
Completed (Fiscal Year 2001)
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| Budget Amount *help |
¥14,400,000 (Direct Cost: ¥14,400,000)
Fiscal Year 2001: ¥2,900,000 (Direct Cost: ¥2,900,000)
Fiscal Year 2000: ¥4,800,000 (Direct Cost: ¥4,800,000)
Fiscal Year 1999: ¥6,700,000 (Direct Cost: ¥6,700,000)
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| Keywords | type 2 diabetes / obesity / OLETF / rat / QTL / congenic strain / Obesity / genome-wide / OLETF rat / loci / Congenic / F344 / Diabetes / Rat / Genetics |
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| Research Abstract |
The Otsuka Long-Evans Tokushima Fatty (OLETF) rat is one of the well-characterized animal models for the study of type II diabetes. Our previous QTL mapping identified 14 loci as candidates for the hyperglycemia in the OLETF rat. Here we generated a series of congenic animals by introgressing into normoglycemic F344 background all 14 OLETF-derived diabetic loci. Subsequent OGTT assay revealed that congenic strains for Nidd1, Nidd2, Nidd3 and Nidd10 showed significantly higher levels of blood glucose in comparison with parental host strain, F344. Furthermore, simultaneously made heterozygote animals for Nidd1, 2 and 10 were normoglycemia, indicating that these loci are recessively inherited. The other nine congenic strains were apparently normoglycemic presumably because the effect of a single locus is too small to be detected by the method employed here. These strains are currently raised on high-fat diet to see if dietary manipulation may help manifest genetic contribution of each locus more clearly. Furthermore, reverse congenic strains whereby F344-derived QTLs are introgressed into OLETF background are also under construction. We believe that these congenic strains should provide useful agents for decomposing complex diabetic traits and for subsequent positional cloning.
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