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Genetic variants in Arhgef11 are associated with kidney injury in the Dahl salt-sensitive rat.
Tuesday,2013-10-01 10:39 America/Los_Angeles — poolea2
| Title | Genetic variants in Arhgef11 are associated with kidney injury in the Dahl salt-sensitive rat. |
| Publication Type | Journal Article |
| Year of Publication | 2012 |
| Authors | Williams, JM, Johnson, AC, Stelloh, C, Dreisbach, AW, Franceschini, N, Regner, KR, Townsend, RR, Roman, RJ, Garrett, MR |
| Journal | Hypertension |
| Volume | 60 |
| Issue | 5 |
| Pagination | 1157-68 |
| Date Published | 2012 Nov |
| ISSN | 1524-4563 |
| Keywords | 1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine, Animals, Animals, Congenic, Blood Pressure, Blotting, Western, Chromosome Mapping, Gene Expression Profiling, Genetic Predisposition to Disease, Guanine Nucleotide Exchange Factors, Humans, Kidney, Kidney Diseases, Male, Polymorphism, Single Nucleotide, Protein Kinase Inhibitors, Proteinuria, Quantitative Trait Loci, Rats, Rats, Inbred Dahl, Rats, Inbred SHR, Renal Circulation, Reverse Transcriptase Polymerase Chain Reaction, rho-Associated Kinases, rhoA GTP-Binding Protein, Signal Transduction |
| Abstract | <p>A previous genetic analysis comparing the Dahl salt-sensitive (S) rat with the spontaneously hypertensive rat identified a major locus on chromosome 2 that influences proteinuria in the S rat. In the present study, blood pressure, proteinuria, and renal hemodynamics were evaluated in congenic strains with small segments of the protective spontaneously hypertensive rat genome on the S background. Proteinuria and renal function were significantly improved in the congenic strains compared with the S. The causative locus interval was narrowed to <375 kb on the basis of congenic strains, haplotype data, comparative mapping, and concordance with human genetic studies. Sequencing of the coding region of genes in this region identified 36 single nucleotide polymorphisms (13 nonsynonymous and 23 synonymous). Gene expression profiling indicated that only a few genes exhibited differential expression. Arhgef11, Pear1, and Sh2d2 were identified as important candidate genes that may be linked to kidney injury in the S rat. In particular, Arhgef11 plays an important role in the activation of the Rho-ROCK signaling pathway. Inhibition of this pathway using fasudil resulted in a significant reduction of proteinuria in treated S rats (compared with untreated S). However, no difference was observed between treated or untreated spontaneously hypertensive rat or congenic strains. The homologous region in humans was found to be associated with estimated glomerular filtration rate in the Candidate Gene Association Resource population. In summary, these findings demonstrate that allelic variants in Arhgef11, acting through the Rho-ROCK pathway, could influence kidney injury in the S as well as provide insight into human kidney disease.</p> |
| DOI | 10.1161/HYPERTENSIONAHA.112.199240 |
| Alternate Journal | Hypertension |
| PubMed ID | 22987919 |
| PubMed Central ID | PMC3505884 |
| Grant List | N01-HC-85085 / HC / NHLBI NIH HHS / United States R01HL59367 / HL / NHLBI NIH HHS / United States HL36279 / HL / NHLBI NIH HHS / United States N01-HC-85081 / HC / NHLBI NIH HHS / United States AG-15928 / AG / NIA NIH HHS / United States AG-20098 / AG / NIA NIH HHS / United States N01-HC-85086 / HC / NHLBI NIH HHS / United States R01 HL089651 / HL / NHLBI NIH HHS / United States HL094446 / HL / NHLBI NIH HHS / United States R01 HL094446 / HL / NHLBI NIH HHS / United States U01HG004402 / HG / NHGRI NIH HHS / United States AG-027058 / AG / NIA NIH HHS / United States N01-HC-85082 / HC / NHLBI NIH HHS / United States N01-HC-35129 / HC / NHLBI NIH HHS / United States N01 HC-55222 / HC / NHLBI NIH HHS / United States R01HL087641 / HL / NHLBI NIH HHS / United States U01 HG004803 / HG / NHGRI NIH HHS / United States N01-HC-85083 / HC / NHLBI NIH HHS / United States N01-HC-75150 / HC / NHLBI NIH HHS / United States N01-HC-85080 / HC / NHLBI NIH HHS / United States N01 HC-15103 / HC / NHLBI NIH HHS / United States N01-HC-45133 / HC / NHLBI NIH HHS / United States N01-HC-85079 / HC / NHLBI NIH HHS / United States HL080295 / HL / NHLBI NIH HHS / United States N01-HC-85239 / HC / NHLBI NIH HHS / United States AG-023629 / AG / NIA NIH HHS / United States R37 HL036279 / HL / NHLBI NIH HHS / United States N01-HC-85084 / HC / NHLBI NIH HHS / United States R01 HL036279 / HL / NHLBI NIH HHS / United States R01HL086694 / HL / NHLBI NIH HHS / United States |