RGD Reference Report - Pathophysiological and genetic characterization of the major diabetes locus in GK rats. - Rat Genome Database

Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

Pathophysiological and genetic characterization of the major diabetes locus in GK rats.

Authors: Galli, J  Fakhrai-Rad, H  Kamel, A  Marcus, C  Norgren, S  Luthman, H 
Citation: Galli J, etal., Diabetes 1999 Dec;48(12):2463-70.
RGD ID: 619677
Pubmed: PMID:10580437   (View Abstract at PubMed)

Genetic studies of the type 2 diabetes-like GK rat have revealed several susceptibility loci for the compound diabetes phenotype. Congenic strains were established for Niddm1, the major quantitative trait locus (QTL) for postprandial glucose levels, by transfer of GK alleles onto the genome of the normoglycemic F344 rat. Despite the polygenic nature of diabetes in GK, the locus-specific diabetes phenotype was retained in the congenic strain Niddmla, containing a GK-derived genomic fragment of 52 cM from the Niddm1 locus. Furthermore, Niddm1 was divided into two non-overlapping loci, physically separated in the two congenic strains Niddmlb and Niddm1i with distinct metabolic phenotypes. Both strains displayed postprandial hyperglycemia and reduced insulin action in isolated adipose cells. Furthermore, Niddm1i already exhibits a pronounced in vivo insulin secretion defect at 65 days, while Niddm1b develops a relative insulin secretory defect at 95 days. This suggests that Niddm1i impairs mechanisms common to insulin secretion in pancreatic B-cells and insulin action in adipocytes. Niddm1b rats show signs of increasing insulin resistance with age associated with obesity, hyperinsulinemia, and dyslipidemia. Moreover, the data indicated nonallelic interaction (epistasis) between Niddm1b and Niddm1i on the postprandial glucose levels. These data emphasize the pathophysiological complexity of diabetes, even within an apparently single QTL, and demonstrate the potential of the GK model in transforming the multifactorial diabetes phenotype into single traits, suitable for positional cloning.



RGD Manual Disease Annotations    Click to see Annotation Detail View

  
Object SymbolSpeciesTermQualifierEvidenceWithNotesSourceOriginal Reference(s)
F344.GK-(D1Arb42a-D1Rat90)/SweRatglucose intolerance  IAGP  RGD 
Niddm43Ratglucose intolerance  IDA  RGD 
Niddm44Ratglucose intolerance  IDA  RGD 
F344.GK-(D1Arb42a-D1Rat90)/SweRathyperglycemia  IAGP  RGD 
F344.GK-(D1Arb42a-D1Rat90)/SweRatInsulin Resistance  IAGP  RGD 

Phenotype Annotations    Click to see Annotation Detail View

Mammalian Phenotype

Object SymbolSpeciesTermQualifierEvidenceWithNotesSourceOriginal Reference(s)
F344.GK-(D1Arb42a-D1Rat90)/SweRatincreased body weight  IAGP compared t F344/DuCrlSweRGD 
F344.GK-(D1Arb42a-D1Rat90)/SweRatincreased circulating glucose level  IAGP compared t F344/DuCrlSweRGD 
F344.GK-(D1Arb42a-D1Rat90)/SweRatincreased circulating HDL cholesterol level  IAGP compared to F344/DuCrlSweRGD 
F344.GK-(D1Mgh10-D1Rat119)/SweRatincreased circulating HDL cholesterol level  IAGP compared to F344/DuCrlSweRGD 
F344.GK-(D1Arb42a-D1Rat90)/SweRatincreased circulating insulin level  IAGP compared t F344/DuCrlSweRGD 
F344.GK-(D1Arb42a-D1Rat90)/SweRatincreased circulating triglyceride level  IAGP compared t F344/DuCrlSweRGD 
F344.GK-(D1Arb42a-D1Rat90)/SweRatincreased epididymal fat pad weight  IAGP compared t F344/DuCrlSweRGD 

Objects Annotated

QTLs
Niddm35  (Non-insulin dependent diabetes mellitus QTL 35)
Niddm43  (Non-insulin dependent diabetes mellitus QTL 43)
Niddm44  (Non-insulin dependent diabetes mellitus QTL 44)

Objects referenced in this article
Strain F344.GK-(D1Mit7-D1Mgh25)/Swe null Rattus norvegicus
QTL Niddm36 Non-insulin dependent diabetes mellitus QTL 36 Rattus norvegicus

Additional Information