RT Journal Article
SR Electronic
T1 Candidate gene scan for Single Nucleotide Polymorphisms involved in the determination of normal variability in human craniofacial morphology
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 060814
DO 10.1101/060814
A1 Mark Barash
A1 Philipp E. Bayer
A1 Angela van Daal
YR 2016
UL http://biorxiv.org/content/early/2016/10/20/060814.abstract
AB Despite intensive research on genetics of the craniofacial morphology using animal models and human craniofacial syndromes, the genetic variation that underpins normal human facial appearance is still largely elusive. Recent development of novel digital methods for capturing the complexity of craniofacial morphology in conjunction with high-throughput genotyping methods, show great promise for unravelling the genetic basis of such a complex trait.As a part of our efforts on detecting genomic variants affecting normal craniofacial appearance, we have implemented a candidate gene approach by selecting 1,201 single nucleotide polymorphisms (SNPs) and 4,732 tag SNPs in over 170 candidate genes and intergenic regions. We used 3-dimentional (3D) facial scans and direct cranial measurements of 587 volunteers to calculate 104 craniofacial phenotypes. Following genotyping by massively parallel sequencing, genetic associations between 2,332 genetic markers and 104 craniofacial phenotypes were tested.An application of a Bonferroni–corrected genome–wide significance threshold produced significant associations between five craniofacial traits and six SNPs. Specifically, associations of nasal width with rs8035124 (15q26.1), cephalic index with rs16830498 (2q23.3), nasal index with rs37369 (5q13.2), transverse nasal prominence angle with rs59037879 (10p11.23) and rs10512572 (17q24.3), and principal component explaining 73.3% of all the craniofacial phenotypes, with rs37369 (5p13.2) and rs390345 (14q31.3) were observed.Due to over-conservative nature of the Bonferroni correction, we also report all the associations that reached the traditional genome-wide p-value threshold (<5.00E-08) as suggestive. Based on the genome-wide threshold, 8 craniofacial phenotypes demonstrated significant associations with 34 intergenic and extragenic SNPs. The majority of associations are novel, except PAX3 and COL11A1 genes, which were previously reported to affect normal craniofacial variation.This study identified the largest number of genetic variants associated with normal variation of craniofacial morphology to date by using a candidate gene approach, including confirmation of the two previously reported genes. These results enhance our understanding of the genetics that determines normal variation in craniofacial morphology and will be of particular value in medical and forensic fields.Author Summary There is a remarkable variety of human facial appearances, almost exclusively the result of genetic differences, as exemplified by the striking resemblance of identical twins. However, the genes and specific genetic variants that affect the size and shape of the cranium and the soft facial tissue features are largely unknown. Numerous studies on animal models and human craniofacial disorders have identified a large number of genes, which may regulate normal craniofacial embryonic development.In this study we implemented a targeted candidate gene approach to select more than 1,200 polymorphisms in over 170 genes that are likely to be involved in craniofacial development and morphology. These markers were genotyped in 587 DNA samples using massively parallel sequencing and analysed for association with 104 traits generated from 3-dimensional facial images and direct craniofacial measurements. Genetic associations (p-values<5.00E-08) were observed between 8 craniofacial traits and 34 single nucleotide polymorphisms (SNPs), including two previously described genes and 26 novel candidate genes and intergenic regions. This comprehensive candidate gene study has uncovered the largest number of novel genetic variants affecting normal facial appearance to date. These results will appreciably extend our understanding of the normal and abnormal embryonic development and impact our ability to predict the appearance of an individual from a DNA sample in forensic criminal investigations and missing person cases.3D3-DimentionalAIMsancestry informative markersASWAfrican ancestry in Southwest USABAMBinary alignment mapBMIBody Mass IndexCAUCaucasianCHBHan Chinese in Beijing, ChinaENGINESENtire Genome INterface for Exploring SnpsEVTExternally visible characteristicDVIDisaster victim identificationFDPForensic DNA phenotypingGWASGenome wide association studiesHWEHardy-Weinberg equilibriumJPTJapanese in Tokyo, JapanLDlinkage disequilibriumlncRNAslong non-coding RNAsLINE-1Long Interspersed Nuclear Element 1MAFMinor allele frequency; measurement errorMEMeasurement errorMDMean differenceOMIMOnline Mendelian Inheritance in ManORFsopen reading framespfSNPPotentially functional SNPPCAPrincipal component analysisRGBRed, Green, Blue (colours)SNPSingle-nucleotide polymorphismSNAPSNP Annotation and Proxy SearchSTRShort tandem repeatTFTranscription factorVCFVariant Call FormatYRIYoruba in Ibadan, Nigeria