Source:http://linkedlifedata.com/resource/pubmed/id/21784893
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2011-8-1
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pubmed:abstractText |
HIVAN1, HIVAN2, and HIVAN3 are nephropathy-susceptibility loci previously identified in the HIV-1 transgenic mouse, a model of collapsing glomerulopathy. The HIVAN1 and HIVAN2 loci modulate expression of Nphs2, which encodes podocin and several other podocyte-expressed genes. To identify additional loci predisposing to nephropathy, we performed a genome-wide scan in 165 backcross mice generated between the nephropathy-sensitive HIV-1-transgenic FVB/NJ (TgFVB) strain and the resistant Balb/cJ (BALB) strain. We identified a major susceptibility locus (HIVAN4) on chromosome 6 G3-F3, with BALB alleles conferring a twofold reduction in severity (peak LOD score = 4.0). Similar to HIVAN1 and HIVAN2, HIVAN4 modulated expression of Nphs2, indicating a common pathway underlying these loci. We independently confirmed the HIVAN4 locus in a sister TgFVB colony that experienced a dramatic loss of nephropathy subsequent to a breeding bottleneck. In this low-penetrance line, 3% of the genome was admixed with BALB alleles, suggesting a remote contamination event. The admixture localized to discrete segments on chromosome 2 and at the HIVAN4 locus. HIVAN4 candidate genes include killer lectin-like receptor genes as well as A2m and Ptpro, whose gene products are enriched in the glomerulus and interact with HIV-1 proteins. In summary, these data identify HIVAN4 as a major quantitative trait locus for nephropathy and a transregulator of Nphs2. Furthermore, similar selective breeding strategies may help identify further susceptibility loci.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1533-3450
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pubmed:author |
pubmed-author:BruggemanLeslie ALA,
pubmed-author:D'AgatiVivette DVD,
pubmed-author:GharaviAli GAG,
pubmed-author:PapetaNataliaN,
pubmed-author:PrakashSindhuriS,
pubmed-author:SedorJohn RJR,
pubmed-author:SterkenRoelR,
pubmed-author:ThomasRobert LRL,
pubmed-author:WuZhenzhenZ,
pubmed-author:ZhengZongyuZ
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pubmed:issnType |
Electronic
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pubmed:volume |
22
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1497-504
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pubmed:meshHeading |
pubmed-meshheading:21784893-Alleles,
pubmed-meshheading:21784893-Animals,
pubmed-meshheading:21784893-Chromosome Mapping,
pubmed-meshheading:21784893-Crosses, Genetic,
pubmed-meshheading:21784893-Female,
pubmed-meshheading:21784893-Genetic Predisposition to Disease,
pubmed-meshheading:21784893-HIV-1,
pubmed-meshheading:21784893-Intracellular Signaling Peptides and Proteins,
pubmed-meshheading:21784893-Kidney Diseases,
pubmed-meshheading:21784893-Lod Score,
pubmed-meshheading:21784893-Male,
pubmed-meshheading:21784893-Membrane Proteins,
pubmed-meshheading:21784893-Mice,
pubmed-meshheading:21784893-Mice, Inbred BALB C,
pubmed-meshheading:21784893-Mice, Transgenic,
pubmed-meshheading:21784893-Models, Genetic
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pubmed:year |
2011
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pubmed:articleTitle |
Identification of the nephropathy-susceptibility locus HIVAN4.
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pubmed:affiliation |
Department of Medicine, Columbia University College of Physicians and Surgeons, New York, New York 10032, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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