par Brotcorne, Anne ;Maenhaut, Geneviève
Référence Proceedings of the National Academy of Sciences of the United States of America, 83, 11, page (3904-3908)
Publication Publié, 1986
Article révisé par les pairs
Résumé : Untargeted UV mutagenesis of bacteriophage λ - i.e., the increased recovery of λ mutants when unirradiated λ infects UV-irradiated Escherichia coli - is thought to be mediated by a transient decrease in DNA replication fidelity, generating mutations in the newly synthesized strands. Using the bacteriophage λ cI857 → λ c mutation system, we provide evidence that the RecA protein, shown previously to be required for this mutagenic pathway, is no longer needed when the LexA protein is inactivated by mutation. We suggest that the error-prone DNA replication responsible for UV-induced untargeted mutagenesis is turned on by the presence of replication-blocking lesions in the host cell DNA and that the RecA protein is required only to derepress the relevant din gene(s). This is in contrast to mutagenesis of irradiated bacteria or irradiated phage λ, in which activated RecA protein has a second role in mutagenesis in addition to the cleavage of the LexA protein. Among the tested din genes, the dinB gene product (in addition to the uvrA and uvrB gene products) was found to be required for untargeted mutagenesis of bacteriophage λ. To our knowledge, a phenotype associated with the dinB gene has not been reported previously.