Literature DB >> 7968917

Mechanisms of transcription-repair coupling and mutation frequency decline.

C P Selby1, A Sancar.   

Abstract

Mutation frequency decline is the rapid and irreversible decline in the suppressor mutation frequency of Escherichia coli cells if the cells are kept in nongrowth media immediately following the mutagenic treatment. The gene mfd, which is necessary for mutation frequency decline, encodes a protein of 130 kDa which couples transcription to excision repair by binding to RNA polymerase and to UvrA, which is the damage recognition subunit of the excision repair enzyme. Although current evidence suggests that transcription-repair coupling is the cause of the preferential repair of the transcribed strand of mRNA encoding genes as well as of suppressor tRNA genes, the decline occurs under stringent response conditions in which the tRNA genes are not efficiently transcribed. Thus, the mechanism of strand-specific repair is well understood, but some questions remain regarding the precise mechanism of mutation frequency decline.

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Year:  1994        PMID: 7968917      PMCID: PMC372971          DOI: 10.1128/mr.58.3.317-329.1994

Source DB:  PubMed          Journal:  Microbiol Rev        ISSN: 0146-0749


  112 in total

1.  RNA polymerase marching backward.

Authors:  G A Kassavetis; E P Geiduschek
Journal:  Science       Date:  1993-02-12       Impact factor: 47.728

2.  Interaction of T7 RNA polymerase with DNA in an elongation complex arrested at a specific psoralen adduct site.

Authors:  Y B Shi; H Gamper; J E Hearst
Journal:  J Biol Chem       Date:  1988-01-05       Impact factor: 5.157

Review 3.  General initiation factors for RNA polymerase II.

Authors:  R C Conaway; J W Conaway
Journal:  Annu Rev Biochem       Date:  1993       Impact factor: 23.643

4.  Inhibitors of DNA synthesis (aphidicolin and araC/HU) prevent the recovery of RNA synthesis after UV-irradiation.

Authors:  L V Mayne
Journal:  Mutat Res       Date:  1984 May-Jun       Impact factor: 2.433

5.  Helicase properties of the Escherichia coli UvrAB protein complex.

Authors:  E Y Oh; L Grossman
Journal:  Proc Natl Acad Sci U S A       Date:  1987-06       Impact factor: 11.205

6.  Differential introduction of DNA damage and repair in mammalian genes transcribed by RNA polymerases I and II.

Authors:  J M Vos; E L Wauthier
Journal:  Mol Cell Biol       Date:  1991-04       Impact factor: 4.272

7.  Transcriptionally active and inactive genes are similarly modified by chemical carcinogens or X-ray in normal human fibroblasts.

Authors:  K Nose; O Nikaido
Journal:  Biochim Biophys Acta       Date:  1984-04-05

8.  Greater susceptibility to mutations in lagging strand of DNA replication in Escherichia coli than in leading strand.

Authors:  X Veaute; R P Fuchs
Journal:  Science       Date:  1993-07-30       Impact factor: 47.728

9.  Effects of DNA lesions on transcription elongation by T7 RNA polymerase.

Authors:  Y H Chen; D F Bogenhagen
Journal:  J Biol Chem       Date:  1993-03-15       Impact factor: 5.157

10.  Human nucleotide excision nuclease removes thymine dimers from DNA by incising the 22nd phosphodiester bond 5' and the 6th phosphodiester bond 3' to the photodimer.

Authors:  J C Huang; D L Svoboda; J T Reardon; A Sancar
Journal:  Proc Natl Acad Sci U S A       Date:  1992-04-15       Impact factor: 11.205

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  58 in total

1.  Modulation of DNA repair by mutations flanking the DNA channel through RNA polymerase.

Authors:  Brigitte W Trautinger; Robert G Lloyd
Journal:  EMBO J       Date:  2002-12-16       Impact factor: 11.598

2.  DNA damage in the nucleosome core is refractory to repair by human excision nuclease.

Authors:  R Hara; J Mo; A Sancar
Journal:  Mol Cell Biol       Date:  2000-12       Impact factor: 4.272

3.  A model for dsDNA translocation revealed by a structural motif common to RecG and Mfd proteins.

Authors:  Akeel A Mahdi; Geoffrey S Briggs; Gary J Sharples; Qin Wen; Robert G Lloyd
Journal:  EMBO J       Date:  2003-02-03       Impact factor: 11.598

4.  Genetic recombination in Bacillus subtilis 168: contribution of Holliday junction processing functions in chromosome segregation.

Authors:  Begoña Carrasco; M Castillo Cozar; Rudi Lurz; Juan C Alonso; Silvia Ayora
Journal:  J Bacteriol       Date:  2004-09       Impact factor: 3.490

5.  Importance of the tmRNA system for cell survival when transcription is blocked by DNA-protein cross-links.

Authors:  H Kenny Kuo; Rachel Krasich; Ashok S Bhagwat; Kenneth N Kreuzer
Journal:  Mol Microbiol       Date:  2010-09-16       Impact factor: 3.501

Review 6.  RNA polymerase between lesion bypass and DNA repair.

Authors:  Alexandra M Deaconescu
Journal:  Cell Mol Life Sci       Date:  2013-06-27       Impact factor: 9.261

7.  Assessing the relative importance of light and the circadian clock in controlling chloroplast translation in Chlamydomonas reinhardtii.

Authors:  Jaesung Lee; David L Herrin
Journal:  Photosynth Res       Date:  2002       Impact factor: 3.573

8.  Ribosomal protein S1 promotes transcriptional cycling.

Authors:  Maxim V Sukhodolets; Susan Garges; Sankar Adhya
Journal:  RNA       Date:  2006-06-14       Impact factor: 4.942

9.  Role of DNA bubble rewinding in enzymatic transcription termination.

Authors:  Joo-Seop Park; Jeffrey W Roberts
Journal:  Proc Natl Acad Sci U S A       Date:  2006-03-21       Impact factor: 11.205

Review 10.  Linkage map of Escherichia coli K-12, edition 10: the traditional map.

Authors:  M K Berlyn
Journal:  Microbiol Mol Biol Rev       Date:  1998-09       Impact factor: 11.056

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