A Genome-Wide Association Study Identifies Five Loci Influencing Facial Morphology in Europeans

Fan Liu(Erasmus MC), Fedde van der Lijn(Erasmus MC), Claudia Schurmann(Universität Greifswald), Gu Zhu(QIMR Berghofer Medical Research Institute), M. Mallar Chakravarty(University of Toronto), Pirro G. Hysi(King's College London), Andreas Wollstein(Erasmus MC), Óscar Lao(Erasmus MC), Marleen de Bruijne(Erasmus MC), M. Arfan Ikram(Erasmus MC), Aad van der Lugt(Erasmus MC), Fernando Rivadeneira(Erasmus MC), André G. Uitterlinden(Erasmus MC), Albert Hofman(Erasmus MC), Wiro J. Niessen(Delft University of Technology), Georg Homuth(Universität Greifswald), Greig I. de Zubicaray(University of Queensland), Katie L. McMahon(National Imaging Facility), Paul M. Thompson(University of California, Los Angeles), Amro Daboul(Universitätsmedizin Greifswald), Ralf Puls(Universitätsmedizin Greifswald), Katrin Hegenscheid(Universitätsmedizin Greifswald), Liisa Bevan(King's College London), Zdenka Pausová(University of Toronto), Sarah E. Medland(QIMR Berghofer Medical Research Institute), Grant W. Montgomery(QIMR Berghofer Medical Research Institute), Margaret J. Wright(QIMR Berghofer Medical Research Institute), Carol Wicking(University of Queensland), Stefan Böehringer(Leiden University Medical Center), Timothy D. Spector(King's College London), Tomáš Paus(University of Toronto), Nicholas G. Martin(QIMR Berghofer Medical Research Institute), Reiner Biffar(Universitätsmedizin Greifswald), Manfred Kayser(Erasmus MC)
PLoS Genetics
September 13, 2012
Cited by 335Open Access
Full Text

Abstract

Inter-individual variation in facial shape is one of the most noticeable phenotypes in humans, and it is clearly under genetic regulation; however, almost nothing is known about the genetic basis of normal human facial morphology. We therefore conducted a genome-wide association study for facial shape phenotypes in multiple discovery and replication cohorts, considering almost ten thousand individuals of European descent from several countries. Phenotyping of facial shape features was based on landmark data obtained from three-dimensional head magnetic resonance images (MRIs) and two-dimensional portrait images. We identified five independent genetic loci associated with different facial phenotypes, suggesting the involvement of five candidate genes--PRDM16, PAX3, TP63, C5orf50, and COL17A1--in the determination of the human face. Three of them have been implicated previously in vertebrate craniofacial development and disease, and the remaining two genes potentially represent novel players in the molecular networks governing facial development. Our finding at PAX3 influencing the position of the nasion replicates a recent GWAS of facial features. In addition to the reported GWA findings, we established links between common DNA variants previously associated with NSCL/P at 2p21, 8q24, 13q31, and 17q22 and normal facial-shape variations based on a candidate gene approach. Overall our study implies that DNA variants in genes essential for craniofacial development contribute with relatively small effect size to the spectrum of normal variation in human facial morphology. This observation has important consequences for future studies aiming to identify more genes involved in the human facial morphology, as well as for potential applications of DNA prediction of facial shape such as in future forensic applications.


Related Papers

No related papers found

Powered by citation graph analysis