In this project, """"""""Haplotype analysis of candidate genes for human pigmentation,"""""""" we seek to understand the relative contribution of allelic variations of candidate genes responsible for variation in human pigmentation. Pigmentation is a classic anthropological trait that has been studied objective using reflectance spectroscopy for over 50 years. Skin pigmentation is likely the trait that shows the largest degree of variability among human populations suggest the action of natural selection. The study of skin pigmentation exist among human populations suggests the action of natural selection. The study of skin pigmentation can help address many problems ranging from understanding skin cancer susceptibility, tanning and sun-burns, and the evolution of light and dark skin. The identification of the genes that determine normal within-population variation in pigmentation and differences between populations is the first essential step in the elucidation of the molecular history of human pigmentation. Combined genetic and epidemiological research on the African American population may reveal potential genetic factors involved in human pigmentation due to the wide range in both genetic and phenotypic variation in this population. This project seeks to provide a better understanding of gene, gene-gene (epistasis), and gene-environment effects on skin color. The goals of this project are to (1) ascertain a cohort of 800-1000 African Americans well-characterized for levels of eumelanin and tanning potential from the Washington, DC metropolitan area; (2) use state-of-the-art DHPLC technology to provide a formal evaluation of single nucleotide polymorphism (SNP) variation in 13 candidate genes for skin color; (3) genotype relevant SNPs within candidate genes and construct haplotypes; (4) exploit the evolutionary history of candidate gene haplotypes in order to determine if haplotypic differences account for phenotypic variation in skin color, and tanning potential; (5) assess whether gene-gene and gene-environment interactions exist by examining if skin color variation is modified after stratification of genetic and/or environmental factors; and (6) determine if molecular signatures for selection are evident across haplotypic backgrounds.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Minority Biomedical Research Support - MBRS (S06)
Project #
2S06GM008016-32
Application #
6547815
Study Section
Special Emphasis Panel (ZGM1)
Project Start
1977-06-01
Project End
2006-07-31
Budget Start
Budget End
Support Year
32
Fiscal Year
2002
Total Cost
Indirect Cost
Name
Howard University
Department
Type
DUNS #
056282296
City
Washington
State
DC
Country
United States
Zip Code
20059
Faruque, Mezbah U; Chen, Guanjie; Doumatey, Ayo P et al. (2017) Transferability of genome-wide associated loci for asthma in African Americans. J Asthma 54:1-8
Johnston, Henry Richard; Hu, Yi-Juan; Gao, Jingjing et al. (2017) Identifying tagging SNPs for African specific genetic variation from the African Diaspora Genome. Sci Rep 7:46398
Kessler, Michael D; Yerges-Armstrong, Laura; Taub, Margaret A et al. (2016) Challenges and disparities in the application of personalized genomic medicine to populations with African ancestry. Nat Commun 7:12521
Liu, Ching-Ti; Raghavan, Sridharan; Maruthur, Nisa et al. (2016) Trans-ethnic Meta-analysis and Functional Annotation Illuminates theĀ Genetic Architecture of Fasting Glucose and Insulin. Am J Hum Genet 99:56-75
Rand, Kristin A; Rohland, Nadin; Tandon, Arti et al. (2016) Whole-exome sequencing of over 4100 men of African ancestry and prostate cancer risk. Hum Mol Genet 25:371-81
Mathias, Rasika Ann; Taub, Margaret A; Gignoux, Christopher R et al. (2016) A continuum of admixture in the Western Hemisphere revealed by the African Diaspora genome. Nat Commun 7:12522
Ehret, Georg B (see original citation for additional authors) (2016) The genetics of blood pressure regulation and its target organs from association studies in 342,415 individuals. Nat Genet 48:1171-1184
Kurian, P; Dunston, G; Lindesay, J (2016) How quantum entanglement in DNA synchronizes double-strand breakage by type II restriction endonucleases. J Theor Biol 391:102-12
Ogunjirin, Adebowale E; Fortunak, Joseph M; Brown, LaVerne L et al. (2015) Competition, Selectivity and Efficacy of Analogs of A-84543 for Nicotinic Acetylcholine Receptors with Repositioning of Pyridine Nitrogen. Neurochem Res 40:2131-42
Winchester, Danyelle; Ricks-Santi, Luisel; Mason, Tshela et al. (2015) SPINK1 Promoter Variants Are Associated with Prostate Cancer Predisposing Alterations in Benign Prostatic Hyperplasia Patients. Anticancer Res 35:3811-9

Showing the most recent 10 out of 152 publications