The log-linear relationship between sexual isolation and sequence divergence in Bacillus transformation is robust

Genetics. 1995 Jul;140(3):917-32. doi: 10.1093/genetics/140.3.917.

Abstract

The relationship between sexual isolation and sequence divergence in Bacillus transformation was previously shown to be log linear. In the present study, we have shown that this relationship is robust with respect to naturally occurring genetic variation among recipient strains of Bacillus subtilis and B. mojavensis. Naturally occurring restriction endonuclease activity was shown not to affect this relationship. Also, seven out of eight recombination mutants tested for their sensitivity to sequence divergence have shown the same relationship between sequence divergence and sexual isolation; a mutant for recH was more sensitive to sequence divergence, suggesting that the product of this gene may be involved in resolution of mismatches in heterogamic transformation. We have also shown that the relationship between sexual isolation and sequence divergence is robust with respect to variation in the conditions of transformation, including variation in the length of donor DNA, the concentration of donor DNA, and intracellular competition between donor-derived and recipient-derived DNA. The robustness of the relationship between sexual isolation and sequence divergence among naturally occurring strains and across transformation conditions allows us to predict the eventual outcome of sequence divergence among B. subtilis and its closest relatives.

Publication types

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

MeSH terms

  • Bacillus / enzymology
  • Bacillus / genetics*
  • Bacillus subtilis / genetics
  • Base Sequence
  • Crosses, Genetic*
  • DNA Primers
  • Genes, Bacterial*
  • Genetic Variation*
  • Genotype
  • Molecular Sequence Data
  • Polymerase Chain Reaction
  • RNA Polymerase II / genetics*
  • Restriction Mapping
  • Species Specificity
  • Transformation, Bacterial*

Substances

  • DNA Primers
  • RNA Polymerase II