Literature DB >> 2347069

The reaction of N-methyl-N-nitrosourea with DNA in B and non-B conformations.

J R Milligan1, S M Skotnicki, M C Archer.   

Abstract

Reaction of N-methyl-N-nitrosourea (MNU) with DNA in B and non-B conformations was investigated using plasmids containing inserts in which the non-B topological isomers could readily be prepared by topoisomerase I catalyzed relaxation in the presence of ethidium. DNA sequences in the Z, cruciform and H conformations were shown to be methylated by MNU at the N7 position of guanines or the N3 position of adenines in a manner that was indistinguishable from the reaction of MNU with the same sequences in the B conformation. Electronic factors rather than steric factors, therefore, appear to dominate methylation of DNA by MNU.

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Year:  1990        PMID: 2347069     DOI: 10.1093/carcin/11.6.947

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


  2 in total

Review 1.  A review of the role of the sequence-dependent electrostatic landscape in DNA alkylation patterns.

Authors:  Barry Gold; Luis M Marky; Michael P Stone; Loren D Williams
Journal:  Chem Res Toxicol       Date:  2006-11       Impact factor: 3.739

2.  The ultimate carcinogen of 4-nitroquinoline 1-oxide does not react with Z-DNA and hyperreacts with B-Z junctions.

Authors:  C Rodolfo; A Lanza; S Tornaletti; G Fronza; A M Pedrini
Journal:  Nucleic Acids Res       Date:  1994-02-11       Impact factor: 16.971

  2 in total

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