Many different RNA molecules are involved in gene expression in cells. In the last few years the secondary structures of several important large RNAs have been deducedd by sequence comparison methods, and it is becoming clear that certain structural motifs are important for the function of these RNAs. The object of this proposal is to study the three dimensional structures and thermodynamics of formation of these structural motifs. Synthetic RNAs will be designed to reproduce these structures in molecules small enough to be amenable to detailed physical studies. The specific motifs to be studied are single base bulges (important for protein recognition); pseudoknots, or base pairing between hairpin loops (probably involved in structural rearrangements of RNAs); and helices containing large proportions of non-canonical base pairs. Using in vitro transcription of cloned synthetic DNA by purified T7 polymerase, 20-30 base RNA molecules containing these structures will be synthesized. 10 milligram amounts can be prepared when necessary. Several kinds ouf physical measurements will be made to determine the structure and thermodynamics of these RNAs: melting temperatures of related RNAs, binding constants for intercalator - RNA or RNA - RNA interctions, and proton NMR spectra. In addition, chemical modification studies of these model RNAs will provide a way to compare their conformations with those of large RNAs.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
1R01GM037005-01
Application #
3291809
Study Section
Biophysics and Biophysical Chemistry A Study Section (BBCA)
Project Start
1986-07-01
Project End
1989-06-30
Budget Start
1986-07-01
Budget End
1987-06-30
Support Year
1
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Johns Hopkins University
Department
Type
Schools of Arts and Sciences
DUNS #
045911138
City
Baltimore
State
MD
Country
United States
Zip Code
21218
Bukhman, Y V; Draper, D E (1997) Affinities and selectivities of divalent cation binding sites within an RNA tertiary structure. J Mol Biol 273:1020-31
Gluick, T C; Gerstner, R B; Draper, D E (1997) Effects of Mg2+, K+, and H+ on an equilibrium between alternative conformations of an RNA pseudoknot. J Mol Biol 270:451-63
Gluick, T C; Wills, N M; Gesteland, R F et al. (1997) Folding of an mRNA pseudoknot required for stop codon readthrough: effects of mono- and divalent ions on stability. Biochemistry 36:16173-86
Draper, D E (1996) Strategies for RNA folding. Trends Biochem Sci 21:145-9
Gluick, T C; Gerstner, R B; Draper, D E (1995) A conformational switch in a regulated mRNA involves tertiary structure. Nucleic Acids Symp Ser :200-2
Kebbekus, P; Draper, D E; Hagerman, P (1995) Persistence length of RNA. Biochemistry 34:4354-7
Morse, S E; Draper, D E (1995) Purine-purine mismatches in RNA helices: evidence for protonated G.A pairs and next-nearest neighbor effects. Nucleic Acids Res 23:302-6
Draper, D E; Gluick, T C (1995) Melting studies of RNA unfolding and RNA-ligand interactions. Methods Enzymol 259:281-305
Gluick, T C; Draper, D E (1994) Thermodynamics of folding a pseudoknotted mRNA fragment. J Mol Biol 241:246-62
Tang, R S; Draper, D E (1994) Bend and helical twist associated with a symmetric internal loop from 5S ribosomal RNA. Biochemistry 33:10089-93

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