Inferring Population History and Demography Using Microsatellites, Mitochondrial DNA, and Major Histocompatibility Complex (MHC) Genes

• Published in: Evolution Vol. 62; no. 6; pp. 1458 - 1468
• Main Authors: Bos, David H., Gopurenko, David, Williams, Rod N., DeWoody, J. Andrew
• Format: Journal Article
• Language: English
• Published: Malden, USA Blackwell Science Inc 01.06.2008; Blackwell Publishing, Inc; Blackwell Publishing Inc; Oxford University Press
• Subjects: Alleles; Ambystoma - genetics; Ambystoma tigrinum; Ambystoma tigrinum tigrinum; Ambystoma, effective population size; Animal populations; Animals; Base Sequence; Demography; DNA Primers - genetics; DNA, Mitochondrial - genetics; Evolution; Evolutionary genetics; Founder Effect; Genetic loci; Genetic markers; Genetic Variation; Genetics, Population; Haplotypes; Haplotypes - genetics; M-ratio; Major Histocompatibility Complex - genetics; Microsatellite Repeats - genetics; Microsatellites; mismatch distribution; Mitochondrial DNA; Molecular Sequence Data; natural selection; neutral evolution; Original s; Population genetics; Population size; Reptiles & amphibians; Selection, Genetic; Sequence Analysis, DNA; Studies
• ISSN: 0014-3820; 1558-5646
• DOI: 10.1111/j.1558-5646.2008.00364.x

Microsatellites and mitochondrial DNA (mtDNA) have traditionally been used in population genetics because of their variability and presumed neutrality, whereas genes of the major histocompatibility complex (MHC) are increasingly of interest because strong selective pressures shape their standing variation. Despite the potential for MHC genes, microsatellites, and mtDNA sequences to complement one another in deciphering population history and demography, the three are rarely used in tandem. Here we report on MHC, microsatellite, and mtDNA variability in a single large population of the eastern tiger salamander (Ambystoma tigrinum tigrinum). We use the mtDNA mismatch distribution and, on microsatellite data, the imbalance index and bottleneck tests to infer aspects of population history and demography. Haplotype and allelic variation was high at all loci surveyed, and heterozygosity was high at the nuclear loci. We find concordance among neutral molecular markers that suggests our study population originated from post-Pleistocene expansions of multiple, fragmented sources that shared few migrants. Differences in Ne estimates derived from haploid and diploid genetic markers are potentially attributable to secondary contact among source populations that experienced rapid mtDNA divergence and comparatively low levels of nuclear DNA divergence. We find strong evidence of natural selection acting on MHC genes and estimate long-term effective population sizes (Ne) that are very large, making small selection intensities significant evolutionary forces in this population.