Literature DB >> 7961656

UVM, an ultraviolet-inducible RecA-independent mutagenic phenomenon in Escherichia coli.

V A Palejwala1, G A Pandya, O S Bhanot, J J Solomon, H S Murphy, P M Dunman, M Z Humayun.   

Abstract

Most mutagenic DNA lesions are noninstructive in the sense that template instruction is either missing or inaccessible during DNA replication, leading to replication arrest. According to the SOS hypothesis, arrested replication induces the expression of SOS factors that force replication past stalled sites at the cost of mutagenesis. We have recently shown that prior UV irradiation of delta recA cells, in which the SOS pathway does not function, enhances mutagenesis at an ethenocytosine residue borne on a circular gapped duplex DNA vector, indicating the existence of an SOS-independent inducible mutagenic phenomenon termed UVM (UV modulation of mutagenesis). In the previous experiments, mutation fixation was expected to occur during gap-filling DNA synthesis. To test whether UVM is observable during normal replication by DNA polymerase III, we have examined mutagenesis at an epsilon C residue borne on M13 single-stranded DNA. By analyzing mutation frequency and specificity using a multiplex sequence assay, we now show that UVM is observable in UV-irradiated recA+, and in delta recA cells. These data indicate that UV irradiation induces a previously unrecognized mutagenic mechanism in Escherichia coli, and that this mechanism is manifested during gap-filling DNA synthesis as well as during normal DNA replication.

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Year:  1994        PMID: 7961656

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  8 in total

1.  Requirement for homologous recombination functions for expression of the mutA mistranslator tRNA-induced mutator phenotype in Escherichia coli.

Authors:  L Ren; A A Al Mamun; M Z Humayun
Journal:  J Bacteriol       Date:  2000-03       Impact factor: 3.490

2.  Escherichia coli cells exposed to streptomycin display a mutator phenotype.

Authors:  L Ren; M S Rahman; M Z Humayun
Journal:  J Bacteriol       Date:  1999-02       Impact factor: 3.490

3.  Induction of the Escherichia coli UVM response by oxidative stress.

Authors:  G Wang; M Z Humayun
Journal:  Mol Gen Genet       Date:  1996-07-19

4.  Escherichia coli cells expressing a mutant glyV (glycine tRNA) gene have a UVM-constitutive phenotype: implications for mechanisms underlying the mutA or mutC mutator effect.

Authors:  H S Murphy; M Z Humayun
Journal:  J Bacteriol       Date:  1997-12       Impact factor: 3.490

5.  SOS and UVM pathways have lesion-specific additive and competing effects on mutation fixation at replication-blocking DNA lesions.

Authors:  M S Rahman; M Z Humayun
Journal:  J Bacteriol       Date:  1999-03       Impact factor: 3.490

6.  Role of mismatch repair in the Escherichia coli UVM response.

Authors:  H S Murphy; V A Palejwala; M S Rahman; P M Dunman; G Wang; M Z Humayun
Journal:  J Bacteriol       Date:  1996-12       Impact factor: 3.490

7.  Functional recA, lexA, umuD, umuC, polA, and polB genes are not required for the Escherichia coli UVM response.

Authors:  V A Palejwala; G E Wang; H S Murphy; M Z Humayun
Journal:  J Bacteriol       Date:  1995-11       Impact factor: 3.490

8.  Alkylating agents induce UVM, a recA-independent inducible mutagenic phenomenon in Escherichia coli.

Authors:  G Wang; V A Palejwala; P M Dunman; D H Aviv; H S Murphy; M S Rahman; M Z Humayun
Journal:  Genetics       Date:  1995-11       Impact factor: 4.562

  8 in total

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