The ultimate objective of the proposed pilot study is to discover genes that influence craniofacial morphology. This will be accomplished through a series of analyses aimed at elucidating fundamental aspects of the genetic architecture of the human craniofacial complex. Understanding the nature of genetic influences on the regions of the cranium is of critical importance to a wide variety of clinicians. As it becomes increasingly possible to incorporate gene therapy and tissue engineering when approaching repair of craniofacial dysmorphology (congenital or acquired), studies that elucidate the genetic underpinnings of continuous phenotypes typifying normal variation in craniofacial morphology are of critical importance. Recent work in humans has revealed that many endocranial traits are significantly heritable, and traits located in different developmental components of the cranium appear to be under differential genetic control. Examination of genetic contributions to normal variation in the craniofacial complex will be addressed through the accomplishment of three specific aims: 1) Collect quantitative measures of craniofacial morphology in order to characterize variation in biomedically-relevant phenotypes. 2) Explore fundamental aspects of the genetic architecture of craniofacial morphology. 3) Identify chromosomal regions (Quantitative Trait Loci; QTL) harboring genes that influence variation in craniofacial measures. Twenty-eight craniometric points will be marked on lateral cephalographs of participants of the Fels Longitudinal Study. Over 10,000 radiographs are available of 1,541 participants from 193 families. A maximum likelihood variance decomposition method for pedigree data using the algorithm implemented in the software program SOLAR is the analytic platform for the analyses. Heritability of each trait will be estimated, and genetic and environmental correlations matrices will be examined for all traits. Finally, linkage analysis will identify quantitative trait loci (QTL) harboring genes influencing variation in adult craniofacial morphology. The proposed study of the genetic architecture of the craniofacial complex will provide information critical in characterizing the genetic underpinnings to normal craniofacial development and morphology.

Agency
National Institute of Health (NIH)
Institute
National Institute of Dental & Craniofacial Research (NIDCR)
Type
Research Project (R01)
Project #
5R01DE016692-04
Application #
7351785
Study Section
Special Emphasis Panel (ZRG1-MOSS-B (02))
Program Officer
Harris, Emily L
Project Start
2005-04-15
Project End
2010-01-31
Budget Start
2008-02-01
Budget End
2010-01-31
Support Year
4
Fiscal Year
2008
Total Cost
$198,514
Indirect Cost
Name
Wright State University
Department
Public Health & Prev Medicine
Type
Schools of Medicine
DUNS #
047814256
City
Dayton
State
OH
Country
United States
Zip Code
45435
Šešelj, Maja; Duren, Dana L; Sherwood, Richard J (2015) Heritability of the Human Craniofacial Complex. Anat Rec (Hoboken) 298:1535-47
Nahhas, Ramzi W; Valiathan, Manish; Sherwood, Richard J (2014) Variation in timing, duration, intensity, and direction of adolescent growth in the mandible, maxilla, and cranial base: the Fels longitudinal study. Anat Rec (Hoboken) 297:1195-207
Sherwood, Richard J; Duren, Dana L; Mahaney, Michael C et al. (2011) A genome-wide linkage scan for quantitative trait loci influencing the craniofacial complex in humans (Homo sapiens sapiens). Anat Rec (Hoboken) 294:664-75
Sherwood, Richard J; Duren, Dana L; Havill, Lorena M et al. (2008) A genomewide linkage scan for quantitative trait loci influencing the craniofacial complex in baboons (Papio hamadryas spp.). Genetics 180:619-28
Sherwood, Richard J; Duren, Dana L; Demerath, Ellen W et al. (2008) Quantitative genetics of modern human cranial variation. J Hum Evol 54:909-14