SOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.

TitleSOS2 and ACP1 Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.
Publication TypeJournal Article
Year of Publication2017
AuthorsLi, M, Li, Y, Weeks, O, Mijatovic, V, Teumer, A, Huffman, JE, Tromp, G, Fuchsberger, C, Gorski, M, Lyytikäinen, L-P, Nutile, T, Sedaghat, S, Sorice, R, Tin, A, Yang, Q, Ahluwalia, TS, Arking, DE, Bihlmeyer, NA, Böger, CA, Carroll, RJ, Chasman, DI, Cornelis, MC, Dehghan, A, Faul, J, Feitosa, MF, Gambaro, G, Gasparini, PP, Giulianini, F, Heid, IM, Huang, J, Imboden, M, Jackson, AU, Jeff, J, Jhun, MA, Katz, R, Kifley, A, Kilpeläinen, TO, Kumar, A, Laakso, M, Li-Gao, R, Lohman, K, Lu, Y, Mägi, R, Malerba, G, Mihailov, E, Mohlke, KL, Mook-Kanamori, DO, Robino, A, Ruderfer, D, Salvi, E, Schick, UM, Schulz, C-A, Smith, AV, Smith, JA, Traglia, M, Yerges-Armstrong, LM, Zhao, W, Goodarzi, MO, Kraja, AT, Liu, C, Wessel, J, Boerwinkle, E, Borecki, IB, Bork-Jensen, J, Bottinger, EP, Braga, D, Brandslund, I, Brody, JA, Campbell, A, Carey, DJ, Christensen, C, Coresh, J, Crook, E, Curhan, GC, Cusi, D, de Boer, IH, de Vries, APJ, Denny, JC, Devuyst, O, Dreisbach, AW, Endlich, K, Esko, T, Franco, OH, Fulop, T, Gerhard, GS, Glümer, C, Gottesman, O, Grarup, N, Gudnason, V, Hansen, T, Harris, TB, Hayward, C, Hocking, LJ, Hofman, A, Hu, FB, Husemoen, LLotte N, Jackson, RD, Jørgensen, T, Jørgensen, ME, Kähönen, M, Kardia, SLR, König, W, Kooperberg, C, Kriebel, J, Launer, LJ, Lauritzen, T, Lehtimäki, T, Levy, D, Linksted, P, Linneberg, A, Liu, Y, Loos, RJF, Lupo, A, Meisinger, C, Melander, O, Metspalu, A, Mitchell, P, Nauck, M, Nürnberg, P, Orho-Melander, M, Parsa, A, Pedersen, O, Peters, A, Peters, U, Polasek, O, Porteous, DJ, Probst-Hensch, NM, Psaty, BM, Qi, L, Raitakari, OT, Reiner, AP, Rettig, R, Ridker, PM, Rivadeneira, F, Rossouw, JE, Schmidt, F, Siscovick, DS, Soranzo, N, Strauch, K, Toniolo, D, Turner, ST, Uitterlinden, AG, Ulivi, S, Velayutham, D, Völker, U, Völzke, H, Waldenberger, M, Wang, JJin, Weir, DR, Witte, D, Kuivaniemi, H, Fox, CS, Franceschini, N, Goessling, W, Köttgen, A, Chu, AY
Corporate AuthorsCHARGE Glycemic-T2D Working Group,, CHARGE Blood Pressure Working Group,
JournalJournal of the American Society of Nephrology
Volume28
Issue3
Pagination981-994
ISSN Number1533-3450
KeywordsAnimals, Exome, Genetic Loci, Genome-Wide Association Study, Glomerular Filtration Rate, Humans, kidney, Protein Tyrosine Phosphatases, Proto-Oncogene Proteins, Son of Sevenless Proteins, Zebrafish
Abstract

Genome-wide association studies have identified >50 common variants associated with kidney function, but these variants do not fully explain the variation in eGFR. We performed a two-stage meta-analysis of associations between genotypes from the Illumina exome array and eGFR on the basis of serum creatinine (eGFRcrea) among participants of European ancestry from the CKDGen Consortium (: 111,666; : 48,343). In single-variant analyses, we identified single nucleotide polymorphisms at seven new loci associated with eGFRcrea (, , and ; <3.7×10), of which most were common and annotated as nonsynonymous variants. Gene-based analysis identified associations of functional rare variants in three genes with eGFRcrea, including a novel association with the SOS Ras/Rho guanine nucleotide exchange factor 2 gene, (=5.4×10 by sequence kernel association test). Experimental follow-up in zebrafish embryos revealed changes in glomerular gene expression and renal tubule morphology in the embryonic kidney of and -knockdowns. These developmental abnormalities associated with altered blood clearance rate and heightened prevalence of edema. This study expands the number of loci associated with kidney function and identifies novel genes with potential roles in kidney formation.

DOI10.1681/ASN.2016020131
Citation Key12133
PubMed ID27920155
PubMed Central IDPMC5328154
Grant ListP30 ES010126 / ES / NIEHS NIH HHS / United States
R01 HL120393 / HL / NHLBI NIH HHS / United States
R21 DK112087 / DK / NIDDK NIH HHS / United States
U01 AG009740 / AG / NIA NIH HHS / United States
R01 DK072193 / DK / NIDDK NIH HHS / United States
S10 OD018522 / OD / NIH HHS / United States
R25 GM062459 / GM / NIGMS NIH HHS / United States
S10 OD020069 / OD / NIH HHS / United States
R01 DK093757 / DK / NIDDK NIH HHS / United States
R01 HL112064 / HL / NHLBI NIH HHS / United States
U01 HL130114 / HL / NHLBI NIH HHS / United States
R01 HL087660 / HL / NHLBI NIH HHS / United States
R01 HL119443 / HL / NHLBI NIH HHS / United States
R01 HL105756 / HL / NHLBI NIH HHS / United States
CZD/16/6/4 / CSO_ / Chief Scientist Office / United Kingdom
MC_PC_U127561128 / MRC_ / Medical Research Council / United Kingdom
UM1 CA182913 / CA / NCI NIH HHS / United States
R21 HL123677 / HL / NHLBI NIH HHS / United States
R01 DK107904 / DK / NIDDK NIH HHS / United States