Substitution rate variation among sites in hypervariable region 1 of human mitochondrial DNA

J Mol Evol. 1993 Dec;37(6):613-23. doi: 10.1007/BF00182747.


More than an order of magnitude difference in substitution rate exists among sites within hypervariable region 1 of the control region of human mitochondrial DNA. A two-rate Poisson mixture and a negative binomial distribution are used to describe the distribution of the inferred number of changes per nucleotide site in this region. When three data sets are pooled, however, the two-rate model cannot explain the data. The negative binomial distribution always fits, suggesting that substitution rates are approximately gamma distributed among sites. Simulations presented here provide support for the use of a biased, yet commonly employed, method of examining rate variation. The use of parsimony in the method to infer the number of changes at each site introduces systematic errors into the analysis. These errors preclude an unbiased quantification of variation in substitution rate but make the method conservative overall. The method can be used to distinguish sites with highly elevated rates, and 29 such sites are identified in hypervariable region 1. Variation does not appear to be clustered within this region. Simulations show that biases in rates of substitution among nucleotides and non-uniform base composition can mimic the effects of variation in rate among sites. However, these factors contribute little to the levels of rate variation observed in hypervariable region 1.

Publication types

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

MeSH terms

  • Biological Evolution*
  • DNA, Mitochondrial / genetics*
  • Genetic Variation*
  • Humans
  • Models, Genetic
  • Mutation


  • DNA, Mitochondrial