The majority of the proposed program is a continuing analysis of the molecular biology of ribonuclease (RNase) P, a ribonucleoprotein enzyme that contains a catalytic RNA involved in tRNA processing. Particular focus is on the RNase P RNAs of Bacillus subtilis and Escherichia coli. The specific elements of this and the other components of the project include: 1. The continued analysis of the RNase P secondary and tertiary structure using phylogenetic structural comparisons, chemical and enzymatic structure mapping, fluorescence energy transfer distance measurements and in vitro mutagenesis. 2. The continued analysis of the RNase P RNA interaction with the RNase P protein and substrates using chemical and enzymatic footprinting, photoactivated crosslinking agents, and in vitro mutagenesis coupled with kinetic analyses. 3. The use of in vitro mutagenesis to engineer simplified versions of active RNase P RNA, thereby to define the RNA elements necessary for catalysis. 4. The analysis of the molecular complexity of RNase P in vivo. 5. The isolation and characterization of an archaebacterial RNase P. 6. The characterization of the excision of an """"""""intron"""""""" from some Salmonella rRNAs. 7. The characterization and functional analysis of low molecular weight RNAs in B. subtilis. The program is health-related in that it will shed new light on RNA functions, including catalysis. The metabolism and many of the roles of RNA are poorly understood, yet are of fundamental significance to growth, development and disease processes, including virus proliferation.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
7R01GM034527-06
Application #
3285700
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1989-07-01
Project End
1993-06-30
Budget Start
1989-07-01
Budget End
1990-06-30
Support Year
6
Fiscal Year
1989
Total Cost
Indirect Cost
Name
Indiana University Bloomington
Department
Type
Schools of Arts and Sciences
DUNS #
006046700
City
Bloomington
State
IN
Country
United States
Zip Code
47402
Kazantsev, Alexei V; Rambo, Robert P; Karimpour, Sina et al. (2011) Solution structure of RNase P RNA. RNA 17:1159-71
Marquez, Steven M; Chen, Julian L; Evans, Donald et al. (2006) Structure and function of eukaryotic Ribonuclease P RNA. Mol Cell 24:445-56
Frank, D N; Harris, M E; Pace, N R (1994) Rational design of self-cleaving pre-tRNA-ribonuclease P RNA conjugates. Biochemistry 33:10800-8
LaGrandeur, T E; Huttenhofer, A; Noller, H F et al. (1994) Phylogenetic comparative chemical footprint analysis of the interaction between ribonuclease P RNA and tRNA. EMBO J 13:3945-52
Harris, M E; Nolan, J M; Malhotra, A et al. (1994) Use of photoaffinity crosslinking and molecular modeling to analyze the global architecture of ribonuclease P RNA. EMBO J 13:3953-63
Brown, J W; Haas, E S; Gilbert, D G et al. (1994) The Ribonuclease P database. Nucleic Acids Res 22:3660-2
Oh, B K; Pace, N R (1994) Interaction of the 3'-end of tRNA with ribonuclease P RNA. Nucleic Acids Res 22:4087-94
Waugh, D S; Pace, N R (1993) Gap-scan deletion analysis of Bacillus subtilis RNase P RNA. FASEB J 7:188-95
Brown, J W; Haas, E S; Pace, N R (1993) Characterization of ribonuclease P RNAs from thermophilic bacteria. Nucleic Acids Res 21:671-9
Zito, K; Huttenhofer, A; Pace, N R (1993) Lead-catalyzed cleavage of ribonuclease P RNA as a probe for integrity of tertiary structure. Nucleic Acids Res 21:5916-20

Showing the most recent 10 out of 50 publications