A worldwide phylogeography for the human X chromosome

• Published in: PloS one 2007-06, Vol.2 (6), p.e557-e557
• Main Authors: Santos-Lopes, Simone S, Pereira, Rinaldo W, Wilson, Ian J, Pena, Sérgio D J
• Format: Article
• Language: English
• Subjects: Alu Elements; Analysis; Biodiversity; Chromosomes; Chromosomes, Human, X - genetics; Chromosomes, Human, Y - genetics; Continents; Deoxyribonucleic acid; DNA; DNA - analysis; DNA - genetics; Evolution; Evolution, Molecular; Evolutionary Biology/Human Evolution; Female; Genes; Genetic aspects; Genetic diversity; Genetic markers; Genetic polymorphisms; Genetic Variation; Genetics and Genomics/Population Genetics; Genetics, Population; Genome, Human; Genomes; Genomics; Geography; Haplotypes; Haplotypes - genetics; Human populations; Humans; Insertion; Linkage Disequilibrium; Male; Males; Markers; Microsatellite Repeats; Microsatellites; Migration; Mitochondrial DNA; Phylogeny; Physical Chromosome Mapping; Polymorphism; Population; Population genetics; Recombination; Trends; X Chromosomes; Y Chromosomes
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0000557

We reasoned that by identifying genetic markers on human X chromosome regions where recombination is rare or absent, we should be able to construct X chromosome genealogies analogous to those based on Y chromosome and mitochondrial DNA polymorphisms, with the advantage of providing information about both male and female components of the population. We identified a 47 Kb interval containing an Alu insertion polymorphism (DXS225) and four microsatellites in complete linkage disequilibrium in a low recombination rate region of the long arm of the human X chromosome. This haplotype block was studied in 667 males from the HGDP-CEPH Human Genome Diversity Panel. The haplotypic diversity was highest in Africa (0.992+/-0.0025) and lowest in the Americas (0.839+/-0.0378), where no insertion alleles of DXS225 were observed. Africa shared few haplotypes with other geographical areas, while those exhibited significant sharing among themselves. Median joining networks revealed that the African haplotypes were numerous, occupied the periphery of the graph and had low frequency, whereas those from the other continents were few, central and had high frequency. Altogether, our data support a single origin of modern man in Africa and migration to occupy the other continents by serial founder effects. Coalescent analysis permitted estimation of the time of the most recent common ancestor as 182,000 years (56,700-479,000) and the estimated time of the DXS225 Alu insertion of 94,400 years (24,300-310,000). These dates are fully compatible with the current widely accepted scenario of the origin of modern mankind in Africa within the last 195,000 years and migration out-of-Africa circa 55,000-65,000 years ago. A haplotypic block combining an Alu insertion polymorphism and four microsatellite markers on the human X chromosome is a useful marker to evaluate genetic diversity of human populations and provides a highly informative tool for evolutionary studies.