RNA-based regulation of genes of tryptophan synthesis and degradation, in bacteria (original) (raw)
- Charles Yanofsky
- Department of Biological Sciences, Stanford University Stanford, California 94305, USA
Abstract
We are now aware that RNA-based regulatory mechanisms are commonly used to control gene expression in many organisms. These mechanisms offer the opportunity to exploit relatively short, unique RNA sequences, in altering transcription, translation, and/or mRNA stability, in response to the presence of a small or large signal molecule. The ability of an RNA segment to fold and form alternative hairpin secondary structures—each dedicated to a different regulatory function—permits selection of specific sequences that can affect transcription and/or translation. In the present paper I will focus on our current understanding of the RNA-based regulatory mechanisms used by Escherichia coli and Bacillus subtilis in controlling expression of the tryptophan biosynthetic operon. The regulatory mechanisms they use for this purpose differ, suggesting that these organisms, or their ancestors, adopted different strategies during their evolution. I will also describe the RNA-based mechanism used by E. coli in regulating expression of its operon responsible for tryptophan degradation, the tryptophanase operon.
- trp operon
- trp suboperon
- aro supraoperon
- tna operon
- transcription attenuation
- T box regulation
- tryptophan as a regulatory signal
- tRNATrp as a regulatory signal
- peptidyl-tRNA
- ribosome mediated regulation
Footnotes
Reprint requests to: Charles Yanofsky, Department of Biological Sciences, Stanford University Stanford, CA 94305, USA; email: yanofsky{at}stanford.edu; fax: (650) 725-8221.
Article published online ahead of print. Article and publication date are at http://www.rnajournal.org/cgi/doi/10.1261/rna.620507.
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