TY - JOUR
T1 - An NMR structural study of deaminated base pairs in DNA
AU - Carbonnaux, Claire
AU - Fazakerley, G. Victor
AU - Sowers, Lawrence C.
N1 - Funding Information:
This work was in part supported by National Institutes of Health grant GM41336 and funds from the City of Hope Cancer Center Core Grant to L.C.S.
PY - 1990/7/25
Y1 - 1990/7/25
N2 - The structurally aberrant base pairs TG, UG and Tl may occur in DNA as a consequence of deamination of 5-methylcytosine, cytosine and adenine respectively. Results of NMR spectroscopic studies are reported here for these deaminated base pairs in a model seven base pair long oligonucleotide duplex. We find that in all three cases, the DNA helix is a normal B form and both mispaired bases are intrahelical and hydrogen bonded with one another in a wobble geometry. Similarly, in all three cases, all sugars are found to be normal C2′ endo in conformation. Symmetric structural perturbations are observed in the helix twist on the 3′ side of the mispaired pyrimidine and on the 5′ side of the mispaired purine. In all three cases, the amino group of the G residue on the 3′ side of the mispaired pyrimidine shows hindered rotation. Although less thermodynamically stable than helices containing only Watson-Crick base pairs, these helices melt normally from the ends and not from the mispair outwards.
AB - The structurally aberrant base pairs TG, UG and Tl may occur in DNA as a consequence of deamination of 5-methylcytosine, cytosine and adenine respectively. Results of NMR spectroscopic studies are reported here for these deaminated base pairs in a model seven base pair long oligonucleotide duplex. We find that in all three cases, the DNA helix is a normal B form and both mispaired bases are intrahelical and hydrogen bonded with one another in a wobble geometry. Similarly, in all three cases, all sugars are found to be normal C2′ endo in conformation. Symmetric structural perturbations are observed in the helix twist on the 3′ side of the mispaired pyrimidine and on the 5′ side of the mispaired purine. In all three cases, the amino group of the G residue on the 3′ side of the mispaired pyrimidine shows hindered rotation. Although less thermodynamically stable than helices containing only Watson-Crick base pairs, these helices melt normally from the ends and not from the mispair outwards.
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U2 - 10.1093/nar/18.14.4075
DO - 10.1093/nar/18.14.4075
M3 - Article
C2 - 2377453
AN - SCOPUS:0025346185
SN - 0305-1048
VL - 18
SP - 4075
JO - Nucleic acids research
JF - Nucleic acids research
IS - 14
ER -