Literature DB >> 8640935

The role of adduct site-specific mutagenesis in understanding how carcinogen-DNA adducts cause mutations: perspective, prospects and problems.

E L Loechler1.   

Abstract

Usually, a particular mutagen/carcinogen forms adducts at many sites in DNA, making it impossible to determine which type of adduct causes which mutation and why. Adduct site-specific mutagenesis studies, in which a single adduct is built into a vector, can be used to overcome this problem. The adduct can be situated in double-stranded DNA, single-stranded DNA or in a single-stranded gap, and the benefit and concerns associated with each are addressed. An adduct site-specific study is most useful when it is compared to a mutagenesis study with its corresponding mutagen/carcinogen. Mutations induced by a particular mutagen/carcinogen can be influenced by DNA sequence context, mutagen/carcinogen dose (and other changes in conditions), level of SOS induction, cell type and other factors. Thus, it is important to match the conditions of the adduct study versus the mutagen/carcinogen study as closely as possible. DNA sequence context can profoundly affect the quantitative and qualitative pattern of adduct mutagenesis, which is addressed. In vitro studies with DNA polymerases, frameshift mutagenesis and semi-targeted mutagenesis, whereby a mutation is induced near but not at the site of the adduct, are each discussed. Finally, the relationship between structural studies on adducts and mutagenesis is considered.

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Year:  1996        PMID: 8640935     DOI: 10.1093/carcin/17.5.895

Source DB:  PubMed          Journal:  Carcinogenesis        ISSN: 0143-3334            Impact factor:   4.944


  5 in total

Review 1.  Investigating the biochemical impact of DNA damage with structure-based probes: abasic sites, photodimers, alkylation adducts, and oxidative lesions.

Authors:  Heidi A Dahlmann; V G Vaidyanathan; Shana J Sturla
Journal:  Biochemistry       Date:  2009-10-13       Impact factor: 3.162

2.  Development and use of an in vitro HSV-tk forward mutation assay to study eukaryotic DNA polymerase processing of DNA alkyl lesions.

Authors:  K A Eckert; S E Hile; P L Vargo
Journal:  Nucleic Acids Res       Date:  1997-04-01       Impact factor: 16.971

3.  DNA polymerase II (polB) is involved in a new DNA repair pathway for DNA interstrand cross-links in Escherichia coli.

Authors:  M Berardini; P L Foster; E L Loechler
Journal:  J Bacteriol       Date:  1999-05       Impact factor: 3.490

4.  A differential mobility spectrometry/mass spectrometry platform for the rapid detection and quantitation of DNA adduct dG-ABP.

Authors:  Amol Kafle; Joshua Klaene; Adam B Hall; James Glick; Stephen L Coy; Paul Vouros
Journal:  Rapid Commun Mass Spectrom       Date:  2013-07-15       Impact factor: 2.419

5.  CHEMICAL SELECTIVITY OF NUCLEOBASE ADDUCTION RELATIVE TO IN VIVO MUTATION SITES ON EXON 7 FRAGMENT OF P53 TUMOR SUPPRESSOR GENE.

Authors:  Spundana Malla; Karteek Kadimisetty; You-Jun Fu; Dharamainder Choudhary; Ingela Jansson; John B Schenkman; James F Rusling
Journal:  Chem Sci       Date:  2015-06-24       Impact factor: 9.825

  5 in total

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