Literature DB >> 19729030

High frequency of genomic deletions induced by Me-lex, a sequence selective N3-adenine methylating agent, at the Hprt locus in Chinese hamster ovary cells.

Debora Russo1, Gilberto Fronza, Laura Ottaggio, Paola Monti, Alberto Inga, Prema Iyer, Barry Gold, Paola Menichini.   

Abstract

We have investigated the mutagenicity induced at the Hprt locus in n class="Species">Chinese hamster ovary (CHO) cells treated with increasing concentrations of Me-lex, a minor groove selective methylating agent that efficiently generates more than 90-95% of 3-MeA DNA adducts. Me-lex treatment was cytotoxic but weakly mutagenic, resulting in up to 7-fold induction above background in the Hprt mutation frequency. The molecular nature of 43 Hprt mutations induced by Me-lex was determined by sequence analysis of the Hprt cDNA and genomic analysis of the gene locus. Base pair substitutions represented about 25% of Me-lex induced mutations. The mutation spectrum revealed a high percentage of genomic deletions (51%) comprising single/multiple exon(s) and even the loss of the complete locus. When the distribution of mutations among different classes was considered, the difference between the spontaneous and Me-lex induced CHO spectra was statistically significant (p<0.012), indicating that the sites where mutations occurred were Me-lex specific. Based upon these results we hypothesize that a large proportion of mutations may result from the processing of 3-MeA, the main adduct induced by Me-lex, within A/T rich sequences in non-coding regions of the Hprt gene. The processing of these lesions by DNA polymerases could result in recombination and genomic deletions, thus representing a severe threat for genome integrity.

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Year:  2009        PMID: 19729030      PMCID: PMC2783936          DOI: 10.1016/j.mrfmmm.2009.08.013

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


  42 in total

1.  Repair in Escherichia coli alkB mutants of abasic sites and 3-methyladenine residues in DNA.

Authors:  S Dinglay; B Gold; B Sedgwick
Journal:  Mutat Res       Date:  1998-03       Impact factor: 2.433

2.  A chemical and genetic approach together define the biological consequences of 3-methyladenine lesions in the mammalian genome.

Authors:  B P Engelward; J M Allan; A J Dreslin; J D Kelly; M M Wu; B Gold; L D Samson
Journal:  J Biol Chem       Date:  1998-02-27       Impact factor: 5.157

3.  The in vitro methylation of DNA by a minor groove binding methyl sulfonate ester.

Authors:  L Encell; D E Shuker; P G Foiles; B Gold
Journal:  Chem Res Toxicol       Date:  1996 Apr-May       Impact factor: 3.739

4.  Multiplex DNA amplification and solid-phase direct sequencing for mutation analysis at the hprt locus in Chinese hamster cells.

Authors:  Z Zu; Y Yu; R A Gibbs; C T Caskey; A W Hsie
Journal:  Mutat Res       Date:  1993-08       Impact factor: 2.433

5.  Molecular characterization of two deletion events involving Alu-sequences, one novel base substitution and two tentative hotspot mutations in the hypoxanthine phosphoribosyltransferase (HPRT) gene in five patients with Lesch-Nyhan syndrome.

Authors:  T Tvrdik; S Marcus; S M Hou; S Fält; P Noori; N Podlutskaja; F Hanefeld; P Strømme; B Lambert
Journal:  Hum Genet       Date:  1998-09       Impact factor: 4.132

6.  Methyl methanesulfonate-induced hprt mutation spectra in the Chinese hamster cell line CHO9 and its xrcc1-deficient derivative EM-C11.

Authors:  C W Op het Veld; J Jansen; M Z Zdzienicka; H Vrieling; A A van Zeeland
Journal:  Mutat Res       Date:  1998-02-26       Impact factor: 2.433

7.  Molecular nature of spontaneous mutations at the hypoxanthine-guanine phosphoribosyltransferase (hprt) locus in Chinese hamster ovary cells.

Authors:  Z Xu; Y Yu; J L Schwartz; M L Meltz; A W Hsie
Journal:  Environ Mol Mutagen       Date:  1995       Impact factor: 3.216

8.  Groove- and sequence-selective alkylation of DNA by sulfonate esters tethered to lexitropsins.

Authors:  Y Zhang; F X Chen; P Mehta; B Gold
Journal:  Biochemistry       Date:  1993-08-10       Impact factor: 3.162

9.  Repair-deficient 3-methyladenine DNA glycosylase homozygous mutant mouse cells have increased sensitivity to alkylation-induced chromosome damage and cell killing.

Authors:  B P Engelward; A Dreslin; J Christensen; D Huszar; C Kurahara; L Samson
Journal:  EMBO J       Date:  1996-02-15       Impact factor: 11.598

10.  Computer program for the analysis of mutational spectra: application to p53 mutations.

Authors:  N F Cariello; W W Piegorsch; W T Adams; T R Skopek
Journal:  Carcinogenesis       Date:  1994-10       Impact factor: 4.944

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  4 in total

1.  XRCC1 deficiency influences the cytotoxicity and the genomic instability induced by Me-lex, a specific inducer of N3-methyladenine.

Authors:  Debora Russo; Gilberto Fronza; Laura Ottaggio; Paola Monti; Chiara Perfumo; Alberto Inga; Prema Iyer; Barry Gold; Paola Menichini
Journal:  DNA Repair (Amst)       Date:  2010-05-14

2.  Probing platinum-adenine-n3 adduct formation with DNA minor-groove binding agents.

Authors:  Lu Rao; Tiffany K West; Gilda Saluta; Gregory L Kucera; Ulrich Bierbach
Journal:  Chem Res Toxicol       Date:  2010-07-19       Impact factor: 3.739

3.  Effect of n3-methyladenine and an isosteric stable analogue on DNA polymerization.

Authors:  Samuel Settles; Ruo-Wen Wang; Gilberto Fronza; Barry Gold
Journal:  J Nucleic Acids       Date:  2010-09-19

4.  Detection of PIGO-deficient cells using proaerolysin: a valuable tool to investigate mechanisms of mutagenesis in the DT40 cell system.

Authors:  Jun Nakamura; Husamettin Gul; Xu Tian; Scott J Bultman; James A Swenberg
Journal:  PLoS One       Date:  2012-03-12       Impact factor: 3.240

  4 in total

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