Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression.
Urmo VõsaAnnique A J ClaringbouldHarm-Jan WestraMarc Jan BonderPatrick DeelenBiao ZengHolger KirstenAshis SahaRoman KreuzhuberSeyhan YazarHarm BruggeRoy OelenDylan H de VriesMonique G P van der WijstSilva KaselaNatalia PervjakovaIsabel AlvesMarie-Julie FavéMawussé AgbessiMark W ChristiansenRick JansenIlkka SeppäläLin TongAlexander TeumerKatharina SchrammGibran HemaniJoost A M VerlouwHanieh YaghootkarReyhan Sönmez FlitmanAndrew Anand BrownViktorija KukushkinaAnette KalnapenkisSina RuegerEleonora PorcuJaanika KronbergJohannes KettunenBernett LeeFutao ZhangTing QiJose Alquicira HernandezWibowo ArindrartoFrank Beutnernull nullnull nullJulia DmitrievaMahmoud ElansaryBenjamin P FairfaxMichel GeorgesBastiaan T HeijmansAlex W HewittMika KähönenYungil KimJulian C KnightPeter KovacsKnut KrohnShuang LiMarkus LoefflerUrko M MarigortaHailang MeiYukihide MomozawaMartina Müller-NuraysidMatthias NauckMichel G NivardBrenda W J H PenninxJonathan K PritchardOlli T RaitakariOlaf RotzschkePieternella Eline SlagboomCoen D A StehouwerMichael StumvollPatrick SullivanPeter A C 't HoenJoachim ThieryAnke TönjesJenny Van DongenMaarten van ItersonJan Herman VeldinkLinus VölkerC A Robert WarmerdamCisca WijmengaMorris A SwertzAnand Kumar AndiappanGrant W MontgomerySamuli RipattiMarkus PerolaZoltan KutalikEmmanouil T DermitzakisSven BergmannTimothy M FraylingJoyce van MeursHolger ProkischHabibul AhsanBrandon L PierceTerho LehtimäkiDorret I BoomsmaBruce M PsatySina A GharibPhilip AwadallaLili A MilaniWillem Hendrik OuwehandKate DownesOliver StegleAlexis BattlePeter M VisscherJian YangMarkus ScholzJoseph PowellGreg GibsonTõnu EskoLude H FrankePublished in: Nature genetics (2021)
Trait-associated genetic variants affect complex phenotypes primarily via regulatory mechanisms on the transcriptome. To investigate the genetics of gene expression, we performed cis- and trans-expression quantitative trait locus (eQTL) analyses using blood-derived expression from 31,684 individuals through the eQTLGen Consortium. We detected cis-eQTL for 88% of genes, and these were replicable in numerous tissues. Distal trans-eQTL (detected for 37% of 10,317 trait-associated variants tested) showed lower replication rates, partially due to low replication power and confounding by cell type composition. However, replication analyses in single-cell RNA-seq data prioritized intracellular trans-eQTL. Trans-eQTL exerted their effects via several mechanisms, primarily through regulation by transcription factors. Expression of 13% of the genes correlated with polygenic scores for 1,263 phenotypes, pinpointing potential drivers for those traits. In summary, this work represents a large eQTL resource, and its results serve as a starting point for in-depth interpretation of complex phenotypes.