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Small, K.S.* ; Hedman, A.K.* ; Grundberg, E.* ; Nica, A.C.* ; Thorleifsson, G.* ; Kong, A.* ; Thorsteindottir, U.* ; Shin, S.Y.* ; Richards, H.B* ; GIANT Consortium (Peters, A. ; Thiering, E. ; Grallert, H. ; Gieger, C. ; Heid, I.M. ; Wichmann, H.-E. ; Illig, T. ; Heinrich, J.) ; MAGIC Investigators (Grallert, H. ; Meisinger, C. ; Gieger, C. ; Thorand, B. ; Wichmann, H.-E. ; Illig, T.) ; DIAGRAM Consortium (Huth, C. ; Grallert, H. ; Gieger, C. ; Klopp, N. ; Meitinger, T. ; Petersen, A.-K. ; Thorand, B. ; Wichmann, H.-E. ; Illig, T.) ; Soranzo, N.* ; Ahmadi, K.R.* ; Lindgren, C.M.* ; Stefansson, K.* ; Dermitzakis, E.T.* ; Deloukas, P.* ; Spector, T.D.* ; McCarthy, M.I.* ; MuTHER Consortium (*)

Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes.

Nat. Genet. 43, 561-564 (2011)
DOI PMC
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Genome-wide association studies have identified many genetic variants associated with complex traits. However, at only a minority of loci have the molecular mechanisms mediating these associations been characterized. In parallel, whereas cis regulatory patterns of gene expression have been extensively explored, the identification of trans regulatory effects in humans has attracted less attention. Here we show that the type 2 diabetes and high-density lipoprotein cholesterol-associated cis-acting expression quantitative trait locus (eQTL) of the maternally expressed transcription factor KLF14 acts as a master trans regulator of adipose gene expression. Expression levels of genes regulated by this trans-eQTL are highly correlated with concurrently measured metabolic traits, and a subset of the trans-regulated genes harbor variants directly associated with metabolic phenotypes. This trans-eQTL network provides a mechanistic understanding of the effect of the KLF14 locus on metabolic disease risk and offers a potential model for other complex traits.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Wide association analysis; Body-mass index; Transciption factors; Insulin-resistance; Twin cohort; Variants; Diseases; Risk
ISSN (print) / ISBN 1061-4036
e-ISSN 1546-1718
Zeitschrift Nature Genetics
Quellenangaben Band: 43, Heft: 6, Seiten: 561-564 Artikelnummer: , Supplement: ,
Verlag Nature Publishing Group
Verlagsort New York, NY
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Research Unit Molecular Epidemiology (AME)
Institute of Epidemiology II (EPI2)
Institute of Genetic Epidemiology (IGE)
Institute of Human Genetics (IHG)
Institute of Epidemiology (EPI)