AI Article Synopsis

  • The study analyzes over 3 million genetic variations from the International HapMap Project to identify regions of the human genome that have undergone positive natural selection.
  • Using advanced methods, researchers pinpointed over 300 candidate regions, specifically narrowing down to 22 strong areas for further scrutiny.
  • The analysis highlights 26 specific gene variations under positive selection, demonstrating similar evolutionary pressures in related genes across different populations, including regions tied to virus infection and traits like skin pigmentation and hair follicle development.

Article Abstract

With the advent of dense maps of human genetic variation, it is now possible to detect positive natural selection across the human genome. Here we report an analysis of over 3 million polymorphisms from the International HapMap Project Phase 2 (HapMap2). We used 'long-range haplotype' methods, which were developed to identify alleles segregating in a population that have undergone recent selection, and we also developed new methods that are based on cross-population comparisons to discover alleles that have swept to near-fixation within a population. The analysis reveals more than 300 strong candidate regions. Focusing on the strongest 22 regions, we develop a heuristic for scrutinizing these regions to identify candidate targets of selection. In a complementary analysis, we identify 26 non-synonymous, coding, single nucleotide polymorphisms showing regional evidence of positive selection. Examination of these candidates highlights three cases in which two genes in a common biological process have apparently undergone positive selection in the same population:LARGE and DMD, both related to infection by the Lassa virus, in West Africa;SLC24A5 and SLC45A2, both involved in skin pigmentation, in Europe; and EDAR and EDA2R, both involved in development of hair follicles, in Asia.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2687721PMC
http://dx.doi.org/10.1038/nature06250DOI Listing

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