A long term goal is to gain an overall understanding of the evolution, gene organization, and regulation of the tRNA multigene family in Escherichia coli. Specific tRNA genes and regulatory DNA will be utilized for detailed studies on gene expression in vivo and in vitro. We are focusing our efforts on the tRNA-leu (leuV) operon and are attempting to elucidate the detailed mechanisms for growth rate dependent regulation and stringent control. We shall compare these results with that obtained using four other E. coli tRNA promoters in order to determine common or unique properties of regulatory DNA. Chemical synthesis and in vitro mutagenesis will be the major approaches employed to identify specific sequences necessary and sufficient for promoter functions. We have shown that some tRNA genes may exhibit a form of feedback control recently shown to be operative for rRNA operons, and will investigate the molecular basis for this phenomenon using appropriate mutant promoters and host strains. In addition, we have shown that the leuV promoter is activated by upstream sequences in DNA; we will investigate this novel parameter in vivo and in vitro using modified promoters in an attempt to determine the molecular basis of activation. This work impinges on several major unanswered questions such as: How are all the tRNA genes of a cell coordinately expressed to ensure accurate protein synthesis? What are the general structural features of the genes? What factors control initiation and termination of transcription here? Ultimately, these studies should permit the engineering of modified genes which will be useful in understanding how tRNA works in the cell.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM025871-10
Application #
3273395
Study Section
Microbial Physiology and Genetics Subcommittee 2 (MBC)
Project Start
1978-12-01
Project End
1991-11-30
Budget Start
1987-12-01
Budget End
1988-11-30
Support Year
10
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Virginia Commonwealth University
Department
Type
Overall Medical
DUNS #
City
Richmond
State
VA
Country
United States
Zip Code
23298
Bauer, B F; Elford, R M; Holmes, W M (1993) Mutagenesis and functional analysis of the Escherichia coli tRNA(1Leu) promoter. Mol Microbiol 7:265-73
Wahab, S Z; Rowley, K O; Holmes, W M (1993) Effects of tRNA(1Leu) overproduction in Escherichia coli. Mol Microbiol 7:253-63
Rowley, K B; Elford, R M; Roberts, I et al. (1993) In vivo regulatory responses of four Escherichia coli operons which encode leucyl-tRNAs. J Bacteriol 175:1309-15
Holmes, W M; Andraos-Selim, C; Roberts, I et al. (1992) Structural requirements for tRNA methylation. Action of Escherichia coli tRNA(guanosine-1)methyltransferase on tRNA(1Leu) structural variants. J Biol Chem 267:13440-5
Vnencak-Jones, C L; Wahab, S Z; Zehner, Z E et al. (1987) A human tRNA(iMet) gene produces multiple transcripts. Mol Cell Biol 7:4134-8