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Detection of differential gene flow from patterns of quantitative variation
1Division of Epidemiology, New York State Department of Health, Albany 12237.
Human Biology
|February 1, 1990
Summary
This study extends a model to assess gene flow using quantitative traits, comparing observed and expected variances to understand population genetic differences. The findings help interpret historical gene flow patterns in diverse human groups.
Area of Science:
- Anthropological Genetics
- Population Genetics
- Quantitative Genetics
Background:
- Microevolutionary forces shape genetic diversity within and between populations.
- The Harpending-Ward model (1982) assesses gene flow by comparing observed and expected heterozygosity.
- Gene flow influences population heterozygosity relative to regional allele frequency centroids.
Purpose of the Study:
- To extend the Harpending-Ward model for analyzing microevolutionary forces using quantitative traits.
- To assess the impact of differential external gene flow on genetic and phenotypic variance.
- To develop methods for estimating the genetic relationship matrix (R) from quantitative traits.
Main Methods:
- Extended the Harpending-Ward model to quantitative traits assuming an equal and additive effects model of inheritance.
- Compared observed and expected genetic or phenotypic variance to evaluate external gene flow.
- Utilized phenotypic covariance matrices as a conservative approach when genetic data is limited.
- Developed new methods for estimating the genetic relationship matrix (R) from quantitative traits.
Main Results:
- The extended model allows for the assessment of differential external gene flow using quantitative trait variances.
- Analyses of dermatoglyphic and anthropometric data from Nepal and Ireland yielded interpretable results.
- Both univariate and multivariate analyses aligned with known historical patterns of gene flow.
Conclusions:
- The extended Harpending-Ward model provides a robust framework for inferring gene flow from quantitative trait data.
- This approach is applicable to diverse datasets, including anthropometric and dermatoglyphic measurements.
- The findings contribute to understanding microevolutionary processes in human populations.