Refinement of the HIVAN1 Susceptibility Locus on Chr. 3A1-A3 via Generation of Sub-Congenic Strains

• Published in: PloS one Vol. 11; no. 10; p. e0163860
• Main Authors: Papeta, Natalia, Patel, Ami, D'Agati, Vivette D, Gharavi, Ali G
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 13-10-2016; Public Library of Science (PLoS)
• Subjects: AIDS-Associated Nephropathy - diagnosis; AIDS-Associated Nephropathy - genetics; AIDS-Associated Nephropathy - pathology; Albuminuria - diagnosis; Albuminuria - genetics; Albuminuria - pathology; Analysis; Animals; Apoptosis; Biology and Life Sciences; Chromosome Mapping; Chromosomes, Human, Pair 3 - genetics; Collaboration; Crosses, Genetic; Development and progression; Disease Models, Animal; Disease susceptibility; Female; FOXO1 protein; Gene expression; Genes; Genetic engineering; Genetic Loci; Genetic Predisposition to Disease; Genomes; Histology; Histone H3; Histopathology; HIV-1 - isolation & purification; Humans; Inflammation; Kidney - metabolism; Kidney - pathology; Kidney diseases; Kidneys; Laboratory animals; Life cycle engineering; Life cycles; Loci; Lysine; Male; Medicine and Health Sciences; Mice; Mice, Congenic; Mice, Transgenic; Nephropathy; Pathogenesis; Proteinuria; Research and Analysis Methods; Rodents; Studies; Susceptibility; Transgenic mice
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0163860

HIV-1 transgenic mice on the FVB/NJ background (TgFVB) represent a validated model of HIV-associated nephropathy (HIVAN). A major susceptibility locus, HIVAN1, was previously mapped to chromosome 3A1-A3 in a cross between TgFVB and CAST/EiJ (CAST) strains, and introgression of a 51.9 Mb segment encompassing HIVAN1 from CAST into TgFVB resulted in accelerated development of nephropathy. We generated three sub-congenic strains carrying CAST alleles in the proximal or distal regions of the HIVAN1 locus (Sub-II, 3.02-38.93 Mb; Sub-III, 38.45-55.1 Mb and Sub-IV, 47.7-55.1 Mb, build 38). At 5-10 weeks of age, histologic injury and proteinuria did not differ between HIV-1 transgenic Sub-II and TgFVB mice. In contrast, HIV-1 transgenic Sub-III and Sub-IV mice displayed up to 4.4 fold more histopathologic injury and 6-fold more albuminuria compared to TgFVB mice, similar in severity to the full-length congenic mice. The Sub-IV segment defines a maximal 7.4 Mb interval for HIVAN1, and encodes 31 protein coding genes: 15 genes have missense variants differentiating CAST from FVB, and 14 genes show differential renal expression. Of these, Frem1, Foxo1, and Setd7 have been implicated in the pathogenesis of nephropathy. HIVAN1 congenic kidneys are histologically normal without the HIV-1 transgene, yet their global transcriptome is enriched for molecular signatures of apoptosis, adenoviral infection, as well as genes repressed by histone H3 lysine 27 trimethylation, a histone modification associated with HIV-1 life cycle. These data refine HIVAN1to 7.4 Mb and identify latent molecular derangements that may predispose to nephropathy upon exposure to HIV-1.