Literature DB >> 12459449

Translesion synthesis by RNA polymerases: occurrence and biological implications for transcriptional mutagenesis.

Paul W Doetsch1.   

Abstract

The genes of all organisms are continuously damaged by extrinsic and intrinsic physical and chemical agents. If the resulting DNA damage is left unrepaired, a number of deleterious biological consequences may result including the production of mutant proteins which can change the cellular phenotype. The majority of DNA damage-induced mutagenesis studies are based on models of DNA polymerase errors occurring in the vicinity of the lesion. In contrast, few studies have addressed the possibility that mutagenesis at the level of transcription (i.e. when RNA polymerase bypasses a lesion and a misincorporation event occurs) may also be an important source of mutant proteins, particularly in nondividing cell populations. This article reviews a number of recent studies on translesion synthesis by RNA polymerases resulting in the production of mutant transcripts (transcriptional mutagenesis). Over a dozen different types of DNA damage are now known to be bypassed with various degrees of efficiency and miscoding abilities by the transcriptional elongation machinery. Some important biological implications of transcriptional mutagenesis are discussed.

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Year:  2002        PMID: 12459449     DOI: 10.1016/s0027-5107(02)00258-0

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


  47 in total

1.  Transcriptional de-repression and Mfd are mutagenic in stressed Bacillus subtilis cells.

Authors:  Holly Anne Martin; Mario Pedraza-Reyes; Ronald E Yasbin; Eduardo A Robleto
Journal:  J Mol Microbiol Biotechnol       Date:  2012-01-13

2.  Importance of steric effects on the efficiency and fidelity of transcription by T7 RNA polymerase.

Authors:  Sébastien Ulrich; Eric T Kool
Journal:  Biochemistry       Date:  2011-11-01       Impact factor: 3.162

Review 3.  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

Review 4.  Base excision repair in nucleosome substrates.

Authors:  Indu Jagannathan; Hope A Cole; Jeffrey J Hayes
Journal:  Chromosome Res       Date:  2006-03-03       Impact factor: 5.239

5.  RNA polymerase II bypass of oxidative DNA damage is regulated by transcription elongation factors.

Authors:  Nicolas Charlet-Berguerand; Sascha Feuerhahn; Stephanie E Kong; Howard Ziserman; Joan W Conaway; Ronald Conaway; Jean Marc Egly
Journal:  EMBO J       Date:  2006-11-16       Impact factor: 11.598

6.  Oxidative DNA damage in osteoarthritic porcine articular cartilage.

Authors:  Antonia F Chen; Catrin M Davies; Ming De Lin; Beverley Fermor
Journal:  J Cell Physiol       Date:  2008-12       Impact factor: 6.384

7.  Transcription of DNA containing the 5-guanidino-4-nitroimidazole lesion by human RNA polymerase II and bacteriophage T7 RNA polymerase.

Authors:  Alexandra Dimitri; Lei Jia; Vladimir Shafirovich; Nicholas E Geacintov; Suse Broyde; David A Scicchitano
Journal:  DNA Repair (Amst)       Date:  2008-06-13

8.  Deoxyuridine in DNA has an inhibitory and promutagenic effect on RNA transcription by diverse RNA polymerases.

Authors:  Junru Cui; Anthony Gizzi; James T Stivers
Journal:  Nucleic Acids Res       Date:  2019-05-07       Impact factor: 16.971

9.  8-Oxo-7,8-dihydroguanine: links to gene expression, aging, and defense against oxidative stress.

Authors:  Zsolt Radak; Istvan Boldogh
Journal:  Free Radic Biol Med       Date:  2010-05-17       Impact factor: 7.376

10.  Transcriptional mutagenesis induced by 8-oxoguanine in mammalian cells.

Authors:  Damien Brégeon; Paul-Antoine Peignon; Alain Sarasin
Journal:  PLoS Genet       Date:  2009-07-24       Impact factor: 5.917

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