Mutacion en e.coli

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Adaptive Reversion of a Frameshift Mutation in Escherichia coli by Simple Base Deletions in Homopolymeric Runs Author(s): Patricia L. Foster and Jeffrey M. Trimarchi Reviewed work(s): Source: Science, New Series, Vol. 265, No. 5170 (Jul. 15, 1994), pp. 407-409 Published by: American Association for the Advancement of Science Stable URL: http://www.jstor.org/stable/2884473 . Accessed: 28/11/201121:13
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made differentmistakes more frequently. However, a second, perhaps additional, explanation appearslikely in view ofthe prevalence of the adaptive mutations in simple repeats. Template-slippagemutaof tions in simplerepeatsare characteristic yeast cells (22) and of hereditarycolon cancer cells (23-25) that are deficient for mismatchrepair.Thus, the post-synthesis caused by apparentpolyhypermutability merase errorsin E. coli cells exposed to misselectioncould also indicatedecreased of matchrepair(26). Downregulation mismatch repairduringadaptivemutationhas been suggested (6, 9, 27) but not in a noncontext of recombination-dependent, templatedadaptivemutations.In both the cancercells and in the bacteriaexposedto nonlethal selection, the ability to mutate adaptivelyconfers the ability to grow and divide. Mechanisticas well as formalsimimayexist (28), laritiesin the two processes which raises thepossibility of bacterial in model systemsfor mutagenesis cancer.
REFERENCESAND NOTES
1. S. E. Luria and M. Delbruck, Genetics 28, 491 (1943). 2. J. Cairns, J. Overbaugh, S. Miller,Nature 335, 142 (1988). 3. J. Cairns and P. L. Foster, Genetics 128, 695 (1991). 4. P. L. Foster and J. Cairns, ibid. 131, 783 (1992). 5. P. L. Foster, Annu. Rev. Microbiol. 47, 467 (1993). 6. R. Jayaraman, J. Genet. 71, 23(1992). 7. B. G. Hall, Genetics 125, 5 (1990). 8. R. S. Harris, S. Longerich, S. M. Rosenberg, Science 264, 258 (1994). 9. P. J. Hastings and S. M. Rosenberg, in Encyclopedia of Immunology, I. M. Roitt and P. J. Delves, Eds. (Saunders, London, 1992), pp. 602-605. 10. D. S. Thaler, J. R. Roth, L. Hirschbein, in The Bacterial Chromosome, K. Drlica and M. Riley, Eds. (American Society for Microbiology,Washington, DC, 1990) pp. 445-456; D. S. Thaler, Trends Ecol. Evol. 9, 108 (1994). 11. A. Grafen, Nature 336, 525 (1988). 12. E. J. Steele, Somatic Selection and Adaptive Evolution (Univ. of Chicago Press, Chicago, 1979); H. S. Rothenfluh and E. J. Steele, Today's Life Science 5, 8 (1993). 13. J. Roth and F. W. Stahl, personal communication; F. W. Stahl, Genetics 132, 865 (1992). 14. N. Maizels,Cell 48, 359 (1991). 15. The frameshift mutation resides in a lac operon that is present on an F' episome in tetracycline-sensitive cells with the chromosomal lac region deleted. We identified intragenic reversion mutations by mating the episome into a /ac-deleted, tetracycline-resistant strain and assaying tetracycline-resistant conjugants for P-galactosidase activity on X-Gal plates. Out of 109adaptive revertants, none was found to be extragenic. An additional 10 lac+ isolates were sequenced directly, without mating, and all but one (a recD isolate) were also found, by sequencing, to be intragenic mutations. 16. Synthetic oligonucleotide primers corresponding to the sequence indicated as primer LacU and complementary to the sequence indicated as primer LacD (Fig. 1) (synthesized on an...
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