Experimental evidence for an alternative to directed mutation in thebgl operon

THE directed mutation hypothesis1–6 suggests that some mutations occur more often when selectively advantageous than when neutral or disadvantageous, challenging the principle that the selective value of a mutation does not affect the rate of its occurrence7–11. Mutations in the bgl operon ofEscherichia coli have been reported to be a case of directed mutation2. E. coli K12 strain Ξ342LD cannot grow on salicin but derivatives with two mutations in the bgl operon, an excision of IS 150 (formally called 1S103; ref. 12) 500 T from bglF and a point mutation or insertion in bglR 13–15 ,grow rapidly on this sugar. When x342LD is grown on a medium containing salicin, bglF excision mutants accumulate to a frequency of >1%, even though these mutants are reportedly2 unable to grow on salicin, and Sal+ double mutants subsequently attain a high frequency. Comparable accumulations of excision mutants and Sal+ double mutants are not observed in the absence of salicin. As salicin is not mutagenic, it has been suggested that excision mutations in bglFmight serve only to create the potential for a secondary selectively advantageous mutation2. We show here, however, that these double mutants can be accounted for by spontaneous mutation to intermediate genotypes in non-growing populations, coupled with slow growth of some of these intermediates on salicin, which enables their populations to reach a size where secondary mutations allowing rapid growth on salicin become common.

[1]  M Slatkin,et al.  Mutation and selection in bacterial populations: alternatives to the hypothesis of directed mutation. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[2]  B. Hall,et al.  Adaptive evolution that requires multiple spontaneous mutations: mutations involving base substitutions. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[3]  R. Lenski,et al.  Are some mutations directed? , 1989, Trends in ecology & evolution.

[4]  S. Benson,et al.  Mutant bias in nonlethal selections results from selective recovery of mutants. , 1991, Genetics.

[5]  J. Overbaugh,et al.  The origin of mutants , 1988, Nature.

[6]  Neville Symonds,et al.  Anticipatory mutagenesis? , 1989, Nature.

[7]  B. Hall Selection, adaptation, and bacterial operons. , 1989, Genome.

[8]  L. Partridge,et al.  Is bacterial evolution random or selective? , 1988, Nature.

[9]  J. Bull,et al.  Origin of mutants disputed , 1988, Nature.

[10]  B. Hall,et al.  Spontaneous point mutations that occur more often when advantageous than when neutral. , 1990, Genetics.

[11]  R. Lenski,et al.  New data on excisions of Mu from E. coli MCS2 cast doubt on directed mutation hypothesis , 1990, Nature.

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

[13]  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.

[14]  A. Wright,et al.  Insertion of DNA activates the cryptic bgl operon in E. coli K12 , 1981, Nature.

[15]  J. Lederberg Replica plating and indirect selection of bacterial mutants: isolation of preadaptive mutants in bacteria by sib selection. , 1989, Genetics.

[16]  If it smells like a unicorn · · · , 1990, Nature.

[17]  F. Stahl A unicorn in the garden , 1988, Nature.

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

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

[20]  D. Hartl,et al.  IS103, a new insertion element in Escherichia coli: characterization and distribution in natural populations. , 1989, Genetics.