SYNTHESIS OF 1,N-2-(1,3-PROPANO)-2'-DEOXYGUANOSINE AND INCORPORATION INTO OLIGODEOXYNUCLEOTIDES - A MODEL FOR EXOCYCLIC ACROLEIN-DNA ADDUCTS

2’-Deoxyguanosine (3) and native DNA both give rise to exocyclic 1,N2-(1,3-propano)-2’-deoxyguanosine adducts 6 and 7 upon treatment with acrolein (1), a known mutagen, in vitro under physiological conditions. The use of synthetic deoxyoligonucleotides containing adduct 6 or 7 could shed light on the mechanism of the mutagenicity of 1 and on the nature of the structural perturbations present in DNA duplexes where they are present. Unfortunately, this is precluded by the instability of 6 and 7 to the conditions of automated DNA synthesis. We have prepared 1,N2-(1,3-propano)-2’-deoxyguanosine (PdG) (8) as a stable model for 6/7. The structure of 8 has been verified by magnetic resonance, ultraviolet spectroscopy, and mass spectrometry. This moiety has been incorporated into oligodeoxynucleotides via solid-state synthesis technology. Negative ion fast atom bombardment (FAB) mass spectrometry of the pentaoligodeoxynucleotide 5’-GT(PdG)CG-3’ verified the identity and position of the modified base. The validity of 8 as a model system for the adduct pair 6/7 in structural and biological studies of DNA duplexes is discussed. © 1990, American Chemical Society. All rights reserved.