Literature DB >> 3025722

Mutagenic DNA repair in Escherichia coli. XIII. Proofreading exonuclease of DNA polymerase III holoenzyme is not operational during UV mutagenesis.

R Woodgate, B A Bridges, G Herrera, M Blanco.   

Abstract

We have introduced a mutD5 mutation (which results in defective 3'-5'-exonuclease activity of the epsilon proofreading subunit of DNA polymerase III holoenzyme) into excision-defective Escherichia coli strains with varying SOS responses to UV light. MutD5 increased the spontaneous mutation frequency in all strains tested, including recA430, umuC122::Tn5, and umuC36 derivatives. It had no effect on UV mutability or immutability in any strain or on misincorporation revealed by delayed photoreversal in UV-irradiated umuC36, umuC122::Tn5, or recA430 bacteria. It is concluded that the epsilon proofreading subunit of DNA polymerase III holoenzyme is excluded, inhibited, or inoperative during misincorporation and mutagenesis after UV.

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Year:  1987        PMID: 3025722     DOI: 10.1016/0167-8817(87)90042-3

Source DB:  PubMed          Journal:  Mutat Res        ISSN: 0027-5107            Impact factor:   2.433


  19 in total

1.  Intrinsic polymerase activities of UmuD'(2)C and MucA'(2)B are responsible for their different mutagenic properties during bypass of a T-T cis-syn cyclobutane dimer.

Authors:  P I O'Grady; A Borden; D Vandewiele; A Ozgenc; R Woodgate; C W Lawrence
Journal:  J Bacteriol       Date:  2000-04       Impact factor: 3.490

2.  T-T cyclobutane dimers are misinstructive, rather than non-instructive, mutagenic lesions.

Authors:  C W Lawrence; S K Banerjee; A Borden; J E LeClerc
Journal:  Mol Gen Genet       Date:  1990-06

3.  Levels of epsilon, an essential replication subunit of Escherichia coli DNA polymerase III, are controlled by heat shock proteins.

Authors:  P L Foster; M G Marinus
Journal:  J Bacteriol       Date:  1992-12       Impact factor: 3.490

4.  Rolling-circle replication of UV-irradiated duplex DNA in the phi X174 replicative-form----single-strand replication system in vitro.

Authors:  O Shavitt; Z Livneh
Journal:  J Bacteriol       Date:  1989-06       Impact factor: 3.490

5.  Requirements for bypass of UV-induced lesions in single-stranded DNA of bacteriophage phi X174 in Salmonella typhimurium.

Authors:  S C Slater; R Maurer
Journal:  Proc Natl Acad Sci U S A       Date:  1991-02-15       Impact factor: 11.205

6.  Efficient translesion replication in the absence of Escherichia coli Umu proteins and 3'-5' exonuclease proofreading function.

Authors:  D Vandewiele; A Borden; P I O'Grady; R Woodgate; C W Lawrence
Journal:  Proc Natl Acad Sci U S A       Date:  1998-12-22       Impact factor: 11.205

7.  SOS-dependent replication past a single trans-syn T-T cyclobutane dimer gives a different mutation spectrum and increased error rate compared with replication past this lesion in uninduced cells.

Authors:  S K Banerjee; A Borden; R B Christensen; J E LeClerc; C W Lawrence
Journal:  J Bacteriol       Date:  1990-04       Impact factor: 3.490

8.  Genetic requirements and mutational specificity of the Escherichia coli SOS mutator activity.

Authors:  I J Fijalkowska; R L Dunn; R M Schaaper
Journal:  J Bacteriol       Date:  1997-12       Impact factor: 3.490

9.  Substitution of mucAB or rumAB for umuDC alters the relative frequencies of the two classes of mutations induced by a site-specific T-T cyclobutane dimer and the efficiency of translesion DNA synthesis.

Authors:  E S Szekeres; R Woodgate; C W Lawrence
Journal:  J Bacteriol       Date:  1996-05       Impact factor: 3.490

10.  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

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