Activation of the bgl operon by adaptive mutation.

In growing Escherichia coli K12 cells, the cryptic bgl operon is activated 98% of the time by insertions of IS1 or IS5 into the control region, designated bglR. The activated bgl operon permits utilization of the beta-glucoside sugar arbutin as a sole carbon and energy source. The bgl operon is also activated by late-occurring mutations during prolonged selection on arbutin. The late-occurring mutations that occurred during prolonged carbon starvation in the presence of arbutin were "adaptive mutations" because they were specific to the presence of arbutin, and they did not occur during prolonged starvation in the absence of arbutin. The spectrum of late-arising mutations differed from that of early-arising, growth-dependent mutations in that 20% of the late-arising mutants resulted from mutations at the hns locus. This provides the first direct evidence for adaptive mutagenesis mediated by the insertion of IS elements. Because no special genetic background is required to select Bgl+ mutants, this affords the opportunity to study IS-element-mediated adaptive mutagenesis in a variety of genetic backgrounds, including the backgrounds of natural isolates of E. coli.

[1]  M Giel,et al.  A mutation in a new gene, bglJ, activates the bgl operon in Escherichia coli K-12. , 1996, Genetics.

[2]  B. Rak,et al.  IS5: a mobile enhancer of transcription in Escherichia coli. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[3]  H. Ochman,et al.  Standard reference strains of Escherichia coli from natural populations , 1984, Journal of bacteriology.

[4]  B. Rak,et al.  Beta-glucoside (bgl) operon of Escherichia coli K-12: nucleotide sequence, genetic organization, and possible evolutionary relationship to regulatory components of two Bacillus subtilis genes , 1987, Journal of bacteriology.

[5]  B. Hall Adaptive evolution that requires multiple spontaneous mutations. I. Mutations involving an insertion sequence. , 1988, Genetics.

[6]  W Arber,et al.  Insertion sequence-related genetic variation in resting Escherichia coli K-12. , 1994, Genetics.

[7]  B. Hall,et al.  Nucleotide sequence, function, activation, and evolution of the cryptic asc operon of Escherichia coli K12. , 1992, Molecular biology and evolution.

[8]  P. Foster Adaptive mutation: the uses of adversity. , 1993, Annual review of microbiology.

[9]  F. M. Stewart,et al.  Fluctuation analysis: the probability distribution of the number of mutants under different conditions. , 1990, Genetics.

[10]  R. Sternglanz,et al.  Escherichia coli DNA topoisomerase I mutants have compensatory mutations in DNA gyrase genes , 1982, Cell.

[11]  Jeffrey H. Miller Experiments in molecular genetics , 1972 .

[12]  M. De Felice,et al.  Cryptic operon for beta-glucoside metabolism in Escherichia coli K12: genetic evidence for a regulatory protein. , 1981, Genetics.

[13]  R. S. Harris,et al.  Adaptive mutation by deletions in small mononucleotide repeats. , 1994, Science.

[14]  J. Trimarchi,et al.  Adaptive reversion of a frameshift mutation in Escherichia coli by simple base deletions in homopolymeric runs. , 1994, Science.

[15]  B. Hall,et al.  Directed evolution of cellobiose utilization in Escherichia coli K12. , 1984, Molecular biology and evolution.

[16]  J. Cairns,et al.  Adaptive reversion of a frameshift mutation in Escherichia coli. , 1991, Genetics.

[17]  A. Grossman,et al.  A collection of strains containing genetically linked alternating antibiotic resistance elements for genetic mapping of Escherichia coli. , 1989, Microbiological reviews.

[18]  M. Delbrück,et al.  Mutations of Bacteria from Virus Sensitivity to Virus Resistance. , 1943, Genetics.