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Misincorporation of 2'-deoxyoxanosine into DNA: a molecular basis for NO-induced mutagenesis derived from theoretical calculations
Author(s) -
Belén Hernández
Publication year - 2000
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/28.24.4873
Subject(s) - guanine , thymine , tautomer , cytosine , dna , biology , mutagenesis , nucleobase , molecular dynamics , aqueous solution , gas phase , ab initio , computational chemistry , chemical physics , thermodynamics , mutation , genetics , stereochemistry , chemistry , nucleotide , physics , gene , organic chemistry
A wide range of theoretical methods, including high level ab initio, density functional, self-consistent reaction field, molecular dynamics and thermodynamic integration calculations, have been used to analyze the mutagenic properties of oxanosine. The major tautomeric forms in the gas phase and aqueous solution have been determined. The ability of oxanosine to recognize thymine and cytosine in the gas phase and in the DNA environment has been compared with that of guanine. A physicochemical explanation for the mutagenic properties of oxanosine is suggested.

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