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Carcinogenic purine N-oxide ester modifies covalently all common bases in polynucleotides
Authors:RA Mathews  G Stöhrer
Institution:Memorial Sloan-Kettering Cancer Center, New York, NY 10021 U.S.A.
Abstract:The carcinogen 1-methyl-3-hydroxyxanthine after esterification binds covalently to polynucleotides, RNA and DNA. All four ribopolynucleotides and poly(dT) are targets. Depending on reaction conditions, covalent binding is greatest to poly(A) followed by poly(U), poly(dT), poly(G), poly(C), RNA and DNA. Maximal covalent modification of DNA is one moiety per 360 nucleotides. All modified polynucleotides, RNA and DNA, except poly guanylic acid have been enzymatically digested and the major adducts characterized as nucleosides.
Keywords:To whom correspondence should be sent at: Sloan-Kettering Institute  Walker Laboratory  145 Boston Post Road  Rye  NY 10580  U  S  A  
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