edoc

SOS2 and ACP1 loci identified through large-scale exome chip analysis regulate kidney development and function

Li, Man and Li, Yong and Weeks, Olivia and Mijatovic, Vladan and Teumer, Alexander and Huffman, Jennifer E. and Tromp, Gerard and Fuchsberger, Christian and Gorski, Mathias and Lyytikäinen, Leo-Pekka and Nutile, Teresa and Sedaghat, Sanaz and Sorice, Rossella and Tin, Adrienne and Yang, Qiong and Ahluwalia, Tarunveer S. and Arking, Dan E. and Bihlmeyer, Nathan A. and Böger, Carsten A. and Carroll, Robert J. and Chasman, Daniel I. and Cornelis, Marilyn C. and Dehghan, Abbas and Faul, Jessica D. and Feitosa, Mary F. and Gambaro, Giovanni and Gasparini, Paolo and Giulianini, Franco and Heid, Iris and Huang, Jinyan and Imboden, Medea and Jackson, Anne U. and Jeff, Janina and Jhun, Min A. and Katz, Ronit and Kifley, Annette and Kilpeläinen, Tuomas O. and Kumar, Ashish and Laakso, Markku and Li-Gao, Ruifang and Lohman, Kurt and Lu, Yingchang and Mägi, Reedik and Malerba, Giovanni and Mihailov, Evelin and Mohlke, Karen L. and Mook-Kanamori, Dennis O. and Robino, Antonietta and Ruderfer, Douglas and Salvi, Erika and Schick, Ursula M. and Schulz, Christina-Alexandra and Smith, Albert V. and Smith, Jennifer A. and Traglia, Michela and Yerges-Armstrong, Laura M. and Zhao, Wei and Goodarzi, Mark O. and Kraja, Aldi T. and Liu, Chunyu and Wessel, Jennifer and Charge Blood Pressure Working Group, and Boerwinkle, Eric and Borecki, Ingrid B. and Bork-Jensen, Jette and Bottinger, Erwin P. and Braga, Daniele and Brandslund, Ivan and Brody, Jennifer A. and Campbell, Archie and Carey, David J. and Christensen, Cramer and Coresh, Josef and Crook, Errol and Curhan, Gary C. and Cusi, Daniele and de Boer, Ian H. and de Vries, Aiko P. J. and Denny, Joshua C. and Devuyst, Olivier and Dreisbach, Albert W. and Endlich, Karlhans and Esko, Tõnu and Franco, Oscar H. and Fulop, Tibor and Gerhard, Glenn S. and Glümer, Charlotte and Gottesman, Omri and Grarup, Niels and Gudnason, Vilmundur and Hansen, Torben and Harris, Tamara B. and Hayward, Caroline and Hocking, Lynne and Hofman, Albert and Hu, Frank B. and Husemoen, Lise Lotte N. and Jackson, Rebecca D. and Jørgensen, Torben and Jørgensen, Marit E. and Kähönen, Mika and Kardia, Sharon L. R. and König, Wolfgang and Kooperberg, Charles and Kriebel, Jennifer and Launer, Lenore J. and Lauritzen, Torsten and Lehtimäki, Terho and Levy, Daniel and Linksted, Pamela and Linneberg, Allan and Liu, Yongmei and Loos, Ruth J. F. and Lupo, Antonio and Meisinger, Christine and Melander, Olle and Metspalu, Andres and Mitchell, Paul and Nauck, Matthias and Nürnberg, Peter and Orho-Melander, Marju and Parsa, Afshin and Pedersen, Oluf and Peters, Annette and Peters, Ulrike and Polasek, Ozren and Porteous, David and Probst-Hensch, Nicole M. and Psaty, Bruce M. and Qi, Lu and Raitakari, Olli T. and Reiner, Alex P. and Rettig, Rainer and Ridker, Paul M. and Rivadeneira, Fernando and Rossouw, Jacques E. and Schmidt, Frank and Siscovick, David and Soranzo, Nicole and Strauch, Konstantin and Toniolo, Daniela and Turner, Stephen T. and Uitterlinden, André G. and Ulivi, Sheila and Velayutham, Dinesh and Völker, Uwe and Völzke, Henry and Waldenberger, Melanie and Wang, Jie Jin and Weir, David R. and Witte, Daniel and Kuivaniemi, Helena and Fox, Caroline S. and Franceschini, Nora and Goessling, Wolfram and Köttgen, Anna and Chu, Audrey Y.. (2017) SOS2 and ACP1 loci identified through large-scale exome chip analysis regulate kidney development and function. Clinical journal of the American Society of Nephrology, 28 (3). pp. 981-994.

Full text not available from this repository.

Official URL: http://edoc.unibas.ch/54734/

Downloads: Statistics Overview

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 (nStage1: 111,666; nStage2: 48,343). In single-variant analyses, we identified single nucleotide polymorphisms at seven new loci associated with eGFRcrea (PPM1J, EDEM3, ACP1, SPEG, EYA4, CYP1A1, and ATXN2L; PStage1<3.7×10(-7)), 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, SOS2 (P=5.4×10(-8) 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 acp1- and sos2-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.
Faculties and Departments:09 Associated Institutions > Swiss Tropical and Public Health Institute (Swiss TPH)
09 Associated Institutions > Swiss Tropical and Public Health Institute (Swiss TPH) > Department of Epidemiology and Public Health (EPH) > Chronic Disease Epidemiology > Genetic Epidemiology of Non-Communicable Diseases (Probst-Hensch)
03 Faculty of Medicine > Departement Public Health > Sozial- und Präventivmedizin > Genetic Epidemiology of Non-Communicable Diseases (Probst-Hensch)
UniBasel Contributors:Probst Hensch, Nicole and Imboden, Medea
Item Type:Article, refereed
Article Subtype:Research Article
Publisher:American Society of Nephrology
ISSN:1555-9041
Note:Publication type according to Uni Basel Research Database: Journal article
Identification Number:
Last Modified:29 May 2017 11:54
Deposited On:29 May 2017 11:54

Repository Staff Only: item control page