RGD Reference Report - Genetic predisposition for glomerulonephritis-induced glomerulosclerosis in rats is linked to chromosome 1. - Rat Genome Database

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Genetic predisposition for glomerulonephritis-induced glomerulosclerosis in rats is linked to chromosome 1.

Authors: Ijpelaar, DH  Schulz, A  Aben, J  Van der Wal, A  Bruijn, JA  Kreutz, R  De Heer, E 
Citation: Ijpelaar DH, etal., Physiol Genomics. 2008 Oct 8;35(2):173-81. Epub 2008 Aug 5.
RGD ID: 2312422
Pubmed: PMID:18682577   (View Abstract at PubMed)
DOI: DOI:10.1152/physiolgenomics.00268.2007   (Journal Full-text)

Genetic factors influence renal disease progression, and several loci have been linked to the spontaneous development of proteinuria and glomerulosclerosis in animal models. However, the role of genetic susceptibility in glomerulonephritis-induced progressive glomerulosclerosis is unknown. In a rat model of mesangial proliferative glomerulonephritis, anti-Thy-1 glomerulonephritis (antiThy1GN), Lewis/Maastricht (Lew/Maa) rats exhibit progression to glomerulosclerosis, whereas in genetically related Lewis/Mollegard (Lew/Moll) rats, glomerular lesions are repaired within 3 wk. The genetic factors underlying this strain-related difference are not known. To identify novel quantitative trait loci (QTL) involved in progression or repair in Lewis rats, 145 female backcross rats [F1(Lew/Maa x Lew/Moll) x Lew/Maa] were studied. After induction of antiThy1GN proteinuria, we determined mesangial activation, the percentage of microaneurysms, and the glomerular damage score for each animal; a genome scan using 187 microsatellite markers was performed. QTL mapping revealed a significant QTL for glomerular damage score on chromosome 1 with a logarithm of odds (LOD) score of 3.9. Homozygosity for Lew/Maa DNA in this region was associated with a higher percentage of damaged glomeruli on day 21. Furthermore, suggestive linkage was found for the percentage of glomeruli with microaneurysms on day 3 on chromosome 1, 6, and 11; for mesangial activation on day 7 on chromosome 18, while proteinuria was suggestively linked to chromosome 5 (day 0), 4 (day 3), and 6 (day 7). This study identifies a QTL on rat chromosome 1 that is significantly linked to progressive glomerulosclerosis after acute glomerulonephritis.

RGD Manual Disease Annotations    Click to see Annotation Detail View
TermQualifierEvidenceWithReferenceNotesSourceOriginal Reference(s)
focal segmental glomerulosclerosis  IAGP 2312422; 2312422; 2312422; 2312422; 2312422; 2312422; 2312422; 2312422 RGD 
proteinuria inducedIAGPanti-Thy1 antibody2312422 RGD 
proteinuria  IAGP 2312422; 2312422; 2312422 RGD 

Phenotype Annotations    Click to see Annotation Detail View

Mammalian Phenotype

TermQualifierEvidenceWithReferenceNotesSourceOriginal Reference(s)
cortical renal glomerulopathies  IDA 2312422; 2312422; 2312422; 2312422; 2312422; 2312422; 2312422; 2312422 RGD 
increased urine protein level  IDA 2312422; 2312422; 2312422 RGD 
kidney microaneurysm inducedIAGPanti-Thy1 antibody2312422compared to LEW/MolRGD 

Objects Annotated

QTLs
Glom17  (Glomerulus QTL 17)
Glom18  (Glomerulus QTL 18)
Glom19  (Glomerulus QTL 19)
Glom20  (Glomerulus QTL 20)
Glom21  (Glomerulus QTL 21)
Pur18  (Proteinuria QTL 18)
Pur19  (Proteinuria QTL 19)
Pur20  (Proteinuria QTL 20)

Strains
LEW/Maas  (NA)
LEW/Mol  (LEW/Mol)


Additional Information