TIGER: The gene expression regulatory variation landscape of human pancreatic islets

Author:

Alonso LorenaORCID,Piron Anthony,Morán Ignasi,Guindo-Martínez Marta,Bonàs-Guarch Sílvia,Atla Goutham,Miguel-Escalada Irene,Royo Romina,Puiggròs Montserrat,Garcia-Hurtado Xavier,Suleiman Mara,Marselli Lorella,Esguerra Jonathan L.S.,Turatsinze Jean-Valéry,Torres Jason M.ORCID,Nylander Vibe,Chen Ji,Eliasson Lena,Defrance Matthieu,Amela Ramon,Mulder Hindrik,Gloyn Anna L.,Groop Leif,Marchetti Piero,Eizirik Decio L.,Ferrer Jorge,Mercader Josep M.,Cnop Miriam,Torrents David,

Abstract

AbstractGWAS have identified more than 700 genetic signals associated with type 2 diabetes (T2D). To gain insight into the underlying molecular mechanisms, we created the Translational human pancreatic Islet Genotype tissue-Expression Resource (TIGER), aggregating >500 human islet RNA-seq and genotyping datasets. We imputed genotypes using 4 reference panels and meta-analyzed cohorts to improve coverage of expression quantitative trait loci (eQTL) and developed a method to combine allele-specific expression across samples (cASE). We identified >1 million islet eQTLs (56% novel), of which 53 colocalize with T2D signals (60% novel). Among them, a low-frequency allele that reduces T2D risk by half increases CCND2 expression. We identified 8 novel cASE colocalizations, among which an SLC30A8 T2D associated variant. We make all the data available through the open-access TIGER portal (http://tiger.bsc.es), which represents a comprehensive human islet genomic data resource to elucidate how genetic variation affects islet function and translate this into therapeutic insight and precision medicine for T2D.

Publisher

Cold Spring Harbor Laboratory

Reference68 articles.

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