The advent of recombinant DNA techniques has resulted in the description of a variety of new categories of genetic markers for our species, in quantities that far exceed the genetic information that previously could be defined by serological and electrophoretic means. Because the techniques used to define these markers are so new, the implications of these new types of genetic markers for human population genetics are only just being perceived. These new markers have revolutionized the study of linkage relationships in Man, and other species, leading to the successful construction of a skeleton linkage map for the entire genome, in just a few years. While the impact of these new markers on human population genetics is likely to be equally profound, so far there have been relatively few attempts to characterize the distribution of the different categories of markers within human populations. We propose to use four distinct categories of DNA polymorphisms to attain to follcwing two scientific objectives: a) To gain insight into the genetic structure of eight different North American Indian tribal populations and evaluate the genetic relationships between them. b) Evaluate theoretical models that characterize the evolutionary distribution of different types of DNA polymorphism over relatively short time scales (< 600 generations, or less). The four categories of DNA polymorphism that will be evaluated include i) single site RFLP's; ii) single locus haplotypes; iii) extensively polymorphic VNTR's; iv) uniparentally transmitted polymorphic (mitochondrial DNA and RFLP's from non pairing regions of the Y chromosome). Each of the eight tribes will be represented by a sample of 75 mother-father-child trios (225 people in all) and the resulting data will be analyzed by traditional methods in population genetics, as well as being used to evaluate new models for the evolutionary distribution of these genetic markers in relatively small human populations.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM041746-01
Application #
3300109
Study Section
Mammalian Genetics Study Section (MGN)
Project Start
1989-04-01
Project End
1992-03-31
Budget Start
1989-04-01
Budget End
1990-03-31
Support Year
1
Fiscal Year
1989
Total Cost
Indirect Cost
Name
University of Utah
Department
Type
Schools of Medicine
DUNS #
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Shields, G F; Schmiechen, A M; Frazier, B L et al. (1993) mtDNA sequences suggest a recent evolutionary divergence for Beringian and northern North American populations. Am J Hum Genet 53:549-62
Ward, R H; Redd, A; Valencia, D et al. (1993) Genetic and linguistic differentiation in the Americas. Proc Natl Acad Sci U S A 90:10663-7
Lundstrom, R; Tavare, S; Ward, R H (1992) Estimating substitution rates from molecular data using the coalescent. Proc Natl Acad Sci U S A 89:5961-5
Lundstrom, R; Tavare, S; Ward, R H (1992) Modeling the evolution of the human mitochondrial genome. Math Biosci 112:319-35
Ward, R H; Frazier, B L; Dew-Jager, K et al. (1991) Extensive mitochondrial diversity within a single Amerindian tribe. Proc Natl Acad Sci U S A 88:8720-4
Arratia, R; Lander, E S; Tavare, S et al. (1991) Genomic mapping by anchoring random clones: a mathematical analysis. Genomics 11:806-27
Weir, B S; Basten, C J (1990) Sampling strategies for distances between DNA sequences. Biometrics 46:551-82