Identification of possible quantitative trait loci responsible for hyperglycaemia after 70% pancreatectomy using a spontaneously diabetogenic rat

The Otsuka Long-Evans Tokushima Fatty (OLETF) rat is an animal model for obese-type non-insulin-dependent diabetes mellitus (NIDDM) in humans. The OLETF rat exhibits sustained hyperglycaemia after partial pancreatectomy, while the normal control rat does not. This difference is thought to be genetic...

Full description

Saved in:
Bibliographic Details
Published inGenetical Research Vol. 73; no. 1; pp. 29 - 36
Main Authors OGINO, T., MORALEJO, D. H., ZHU, M., TOIDE, K., WEI, S., WEI, K., YAMADA, T., MIZUNO, A., MATSUMOTO, K., SHIMA, K.
Format Journal Article
LanguageEnglish
Published England Cambridge University Press 01.02.1999
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:The Otsuka Long-Evans Tokushima Fatty (OLETF) rat is an animal model for obese-type non-insulin-dependent diabetes mellitus (NIDDM) in humans. The OLETF rat exhibits sustained hyperglycaemia after partial pancreatectomy, while the normal control rat does not. This difference is thought to be genetically determined and to be caused by impairment of β-cell regrowth, a possible event involved in the pathogenesis of NIDDM. Our investigation was designed to identify quantitative trait loci (QTL) responsible for post-pancreatectomy hyperglycaemia by performing a genome-wide scan in an F2 intercross obtained by mating the OLETF and Fischer-344 (F344) rats. We have identified three possible QTL on rat chromosomes (Chrs) 3, 14 and 19 that account for a total of approximately 75% of the genetic variance in the F2. For the QTL on Chr 14, the OLETF allele corresponds with increased glucose levels, as expected. Surprisingly, for the QTL on Chr 19, the F344 allele corresponds with increased glucose levels. The Chr 3 QTL exhibits heterosis, heterozygotes showing significantly higher glucose levels than OLETF or F344 homozygotes. We also found evidence for interaction (epistasis) between the QTL on Chrs 14 and 19.
Bibliography:PII:S0016672398003644
ark:/67375/6GQ-81GFHP78-6
istex:CEB8035DD4A3CF8E06FF13C4F6C1952E8E5FBF4E
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0016-6723
1469-5073
DOI:10.1017/S0016672398003644