Title
Novel genetic loci affecting facial shape variation in humans
Date Issued
01 November 2019
Access level
open access
Resource Type
journal article
Author(s)
Xiong Z.
Dankova G.
Howe L.J.
Lee M.K.
Hysi P.G.
De Jong M.A.
Zhu G.
Adhikar K.
Li D.
Li Y.
Pan B.
Feingold E.
Marazita M.L.
Shaffer J.R.
McAloney K.
Xu S.
Jin L.
Wang S.
De Vri F.M.
Lendemeije B.
Richmond S.
Zhurov A.
Lewis S.
Sharp G.
Paternoster L.
Thompson H.
Gonzalez-Jose R.
Catira Bortolini M.
Canizales-Quinteros S.
Bedoya G.
Rothhammer F.
Uitterlinden A.G.
Ikram M.A.
Wolvius E.B.
Kushner S.A.
Nijsten T.
Palstra R.J.
Boehringer S.
Medland S.E.
Tang K.
Ruiz-Linares A.
Martin N.G.
Spector T.D.
Stergiakouli E.
Weinberg S.M.
Liu F.
Kayser M.
Publisher(s)
eLife Sciences Publications Ltd
Abstract
The human face represents a combined set of highly heritable phenotypes, but knowledge on its genetic architecture remains limited, despite the relevance for various fields. A series of genome wide association studies on 78 facial shape phenotypes quantified from 3-dimensional facial images of 10,115 Europeans identified 24 genetic loci reaching study-wide suggestive association (p<5x10-8), among which 17 were previously unreported. A follow-up multi-ethnic study in additional 7,917 individuals confirmed 10 loci including 6 unreported ones (padjusted<2.1x10-3). A global map of derived polygenic face scores assembled facial features in major continental groups consistent with anthropological knowledge. Analyses of epigenomic datasets from cranial neural crest cells revealed abundant cis-regulatory activities at the face-associated genetic loci. Luciferase reporter assays in neural crest progenitor cells highlighted enhancer activities of several face-associated DNA variants. These results substantially advance our understanding of the genetic basis underlying human facial variation and provide candidates for future in-vivo functional studies.
Volume
8
Language
English
OCDE Knowledge area
Genética, Herencia Genética humana
Scopus EID
2-s2.0-85076382380
PubMed ID
Source
eLife
ISSN of the container
2050084X
Sponsor(s)
University of Bristol and the UK Medical Research Council (MC_UU_00011/1). S.E.M. is supported by XDB13041000 to S.W. and S.X., QYZDJ-SSW-SYS009 to S.X.), the National Basic Research Program “Wanren Jihua” Project to S.X., the National Thousand Young Talents Award and the Max Planck- This work was financially supported in part by the European Union’s Horizon 2020 Research and the University of Washington was provided by contract #HHSN268201200008I from the National Innovation Programme under grant agreement No 740580 (VISAGE). Z.X. is supported by the China (grant number 16JC1400504 to L.J. and S.W.), the Chinese Academy of Sciences (grant number funding through the following grant: R01-DD000295. Funding for initial genomic data cleaning by (16XD1404700), the National Key Research and Development Program (2016YFC0906403 to S.X. and The ALSPAC was supported by The UK Medical Research Council and Wellcome (Grant ref: The Rotterdam Study is supported by the Netherlands Organization of Scientific Research NWO he TwinsUK study is funded by the Wellcome Trust, Medical Research Council, European Union Chinese National Thousand Young Talents Award, the National Natural Science Foundation of China (NSFC) (91651507), the National Key Research and Development Program of China Investments (nr. 175.010.2005.011, 911-03-012). This study is funded by the Research Institute for The UYG studies were supported by the National Natural Science Foundation of China (NSFC) an NHMRC fellowship APP1103623. F.L. is supported by an Erasmus University Fellowship, the supported by the Erasmus MC and Erasmus University Rotterdam; the Netherlands Organization.
Sources of information: Directorio de Producción Científica Scopus