| Literature DB >> 31995762 |
Luz D Orozco1, Hsu-Hsin Chen2, Christian Cox3, Kenneth J Katschke3, Rommel Arceo4, Carmina Espiritu4, Patrick Caplazi4, Sarajane Saturnio Nghiem4, Ying-Jiun Chen5, Zora Modrusan5, Amy Dressen6, Leonard D Goldstein7, Christine Clarke1, Tushar Bhangale6, Brian Yaspan6, Marion Jeanne3, Michael J Townsend8, Menno van Lookeren Campagne9, Jason A Hackney10.
Abstract
Age-related macular degeneration (AMD) is a leading cause of vision loss. To better understand disease pathogenesis and identify causal genes in GWAS loci for AMD risk, we present a comprehensive database of human retina and retinal pigment epithelium (RPE). Our database comprises macular and non-macular RNA sequencing (RNA-seq) profiles from 129 donors, a genome-wide expression quantitative trait loci (eQTL) dataset that includes macula-specific retina and RPE/choroid, and single-nucleus RNA-seq (NucSeq) from human retina and RPE with subtype resolution from more than 100,000 cells. Using NucSeq, we find enriched expression of AMD candidate genes in RPE cells. We identify 15 putative causal genes for AMD on the basis of co-localization of genetic association signals for AMD risk and eye eQTL, including the genes TSPAN10 and TRPM1. These results demonstrate the value of our human eye database for elucidating genetic pathways and potential therapeutic targets for ocular diseases.Entities:
Keywords: AMD; GWAS; NucSeq; RNA-seq; age-related macular degeneration; eQTL; retina; retinal pigment epithelium; single cell
Year: 2020 PMID: 31995762 DOI: 10.1016/j.celrep.2019.12.082
Source DB: PubMed Journal: Cell Rep Impact factor: 9.423