Modified nucleosides present in DNA have been implicated in such diverse areas as mutagenesis, carcinogenesis, protein-DNA recognition, and transcription. In addition, it is now known that DNA is conformationally flexible, and that conformational differences are critically important to DNA function. In order to begin to understand these effects it is necessary to have model systems - specifically modified oligonucleotides. However, such molecules have been largely unavailable due both to the lack of appropriate modified nucleosides and to the rigors of oligonucleotide synthesis and purification. The long term goals of this project are to develop and demonstrate the synthetic strategies and purification methodologies necessary for the synthesis and utilization of specifically modified oligonucleotides. The molecules that are proposed will have immediate impact on understanding of DNA base pairing, conformation, and structure/function relationships. In addition, the procedures developed will provide access to other modified oligonucleotides, designed to answer specific questions about DNA. The modified nucleosides to be incorporated will include: 06-methyl- and 06-ethyl deoxyguanosine, N6-methyl- and N6-methoxydeoxyadenosine, 2-aminopurine deoxyriboside, and 15N labelled deoxyadenosine, deoxyguanosine and 06-alkyldeoxyguanosine. In all cases the routes devised will be amenable to large scale synthesis so that the modified nucleosides produced will be usable for oligonucleotide synthesis. In order to incorporate these modified nucleosides into oligonucleotides we will devise synthetic strategies that are more nucleoside efficient than are present approaches. The modified oligonucleotides will then be """"""""paired"""""""" with a set of complementary oligonucleotides, so that all possible combinations with the modified nucleoside and its nearest neighbors will be present. In addition, we will rigorously examine these synthetic oligonucleotides to attempt to isolate and identify the minor side reactions which accompany oligonucleotide synthesis. Side reactions have been a particular problem with certain modified nucleosides, and also accompany standard oligonucleotide synthesis.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM031483-06
Application #
3279511
Study Section
Medicinal Chemistry Study Section (MCHA)
Project Start
1983-03-01
Project End
1989-06-30
Budget Start
1988-07-01
Budget End
1989-06-30
Support Year
6
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Rutgers University
Department
Type
Schools of Arts and Sciences
DUNS #
038633251
City
New Brunswick
State
NJ
Country
United States
Zip Code
08901
Li, Tsai-Kun; Barbieri, Christopher M; Lin, Hsin-Chin et al. (2004) Drug targeting of HIV-1 RNA.DNA hybrid structures: thermodynamics of recognition and impact on reverse transcriptase-mediated ribonuclease H activity and viral replication. Biochemistry 43:9732-42
Shallop, Anthony J; Gaffney, Barbara L; Jones, Roger A (2003) Use of 13C as an indirect tag in 15N specifically labeled nucleosides. Syntheses of [8-13C-1,7,NH2-15N3]adenosine, -guanosine, and their deoxy analogues. J Org Chem 68:8657-61
Barbieri, Christopher M; Li, Tsai-Kun; Guo, Susan et al. (2003) Aminoglycoside complexation with a DNA.RNA hybrid duplex: the thermodynamics of recognition and inhibition of RNA processing enzymes. J Am Chem Soc 125:6469-77
Lorigan, G A; McNamara, R; Jones, R A et al. (1999) Magnitudes and orientations of the 15N chemical shift tensor of [1-15N]-2'-deoxyguanosine determined on a polycrystalline sample by two-dimensional solid-state NMR spectroscopy. J Magn Reson 140:315-9
Vojtechovsky, J; Eaton, M D; Gaffney, B et al. (1995) Structure of a new crystal form of a DNA dodecamer containing T.(O6Me)G base pairs. Biochemistry 34:16632-40
Parkinson, G N; Arvanitis, G M; Lessinger, L et al. (1995) Crystal and molecular structure of a new Z-DNA crystal form: d[CGT(2-NH2-A)CG] and its platinated derivative. Biochemistry 34:15487-95
Ginell, S L; Vojtechovsky, J; Gaffney, B et al. (1994) Crystal structure of a mispaired dodecamer, d(CGAGAATTC(O6Me)GCG)2, containing a carcinogenic O6-methylguanine. Biochemistry 33:3487-93
Erie, D A; Suri, A K; Breslauer, K J et al. (1993) Theoretical predictions of DNA hairpin loop conformations: correlations with thermodynamic and spectroscopic data. Biochemistry 32:436-54
Schneider, B; Ginell, S L; Jones, R et al. (1992) Crystal and molecular structure of a DNA fragment containing a 2-aminoadenine modification: the relationship between conformation, packing, and hydration in Z-DNA hexamers. Biochemistry 31:9622-8
Wang, Y; Jin, R; Gaffney, B et al. (1991) Characterization by 1H NMR of glycosidic conformations in the tetramolecular complex formed by d(GGTTTTTGG). Nucleic Acids Res 19:4619-22

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