| Literature DB >> 30057032 |
Christopher E Gillies1, Rosemary Putler1, Rajasree Menon2, Edgar Otto3, Kalyn Yasutake1, Viji Nair3, Paul Hoover4, David Lieb5, Shuqiang Li5, Sean Eddy3, Damian Fermin1, Michelle T McNulty1, Nir Hacohen4, Krzysztof Kiryluk6, Matthias Kretzler7, Xiaoquan Wen8, Matthew G Sampson9.
Abstract
Expression quantitative trait loci (eQTL) studies illuminate the genetics of gene expression and, in disease research, can be particularly illuminating when using the tissues directly impacted by the condition. In nephrology, there is a paucity of eQTL studies of human kidney. Here, we used whole-genome sequencing (WGS) and microdissected glomerular (GLOM) and tubulointerstitial (TI) transcriptomes from 187 individuals with nephrotic syndrome (NS) to describe the eQTL landscape in these functionally distinct kidney structures. Using MatrixEQTL, we performed cis-eQTL analysis on GLOM (n = 136) and TI (n = 166). We used the Bayesian "Deterministic Approximation of Posteriors" (DAP) to fine-map these signals, eQTLBMA to discover GLOM- or TI-specific eQTLs, and single-cell RNA-seq data of control kidney tissue to identify the cell type specificity of significant eQTLs. We integrated eQTL data with an IgA Nephropathy (IgAN) GWAS to perform a transcriptome-wide association study (TWAS). We discovered 894 GLOM eQTLs and 1,767 TI eQTLs at FDR < 0.05. 14% and 19% of GLOM and TI eQTLs, respectively, had >1 independent signal associated with its expression. 12% and 26% of eQTLs were GLOM specific and TI specific, respectively. GLOM eQTLs were most significantly enriched in podocyte transcripts and TI eQTLs in proximal tubules. The IgAN TWAS identified significant GLOM and TI genes, primarily at the HLA region. In this study, we discovered GLOM and TI eQTLs, identified those that were tissue specific, deconvoluted them into cell-specific signals, and used them to characterize known GWAS alleles. These data are available for browsing and download via our eQTL browser, "nephQTL."Entities:
Keywords: eQTL; expression quantitative trait loci; focal segmental glomerulosclerosis; genomics; glomerulus; kidney; minimal change disease; nephrotic syndrome; podocyte; proteinuria; single-cell RNA sequencing
Mesh:
Year: 2018 PMID: 30057032 PMCID: PMC6081280 DOI: 10.1016/j.ajhg.2018.07.004
Source DB: PubMed Journal: Am J Hum Genet ISSN: 0002-9297 Impact factor: 11.025