On the estimation of genome-wide heterozygosity using molecular markers

J Hered. 2005 Mar-Apr;96(2):85-8. doi: 10.1093/jhered/esi017. Epub 2004 Dec 23.

Abstract

Coltman and Slate (2003) recently performed a meta-analysis on studies that investigated the association between genetic variation at microsatellite loci and phenotypic trait variation. One factor not explicitly addressed in their meta-analysis is the actual estimation of genome-wide heterozygosity via molecular markers. Many authors still associate marker-estimated heterozygosity with genome-wide heterozygosity, despite allozyme-based evidence that such correlations are usually very weak or nonexistent. Here, we show that genome-wide heterozygosity is poorly estimated not only by allozymes but also by microsatellite loci and by single-nucleotide polymorphisms (SNPs). Thus, associations between fitness (or other phenotypes) and heterozygosity should be established firmly on causative factors and not on simple correlations.

Publication types

  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • Genetic Carrier Screening*
  • Genetic Markers
  • Genome*
  • Isoenzymes
  • Microsatellite Repeats / genetics
  • Models, Genetic*
  • Polymorphism, Single Nucleotide / genetics

Substances

  • Genetic Markers
  • Isoenzymes