Engineered riboregulators enable post-transcriptional control of gene expression
- 20 June 2004
- journal article
- research article
- Published by Springer Nature in Nature Biotechnology
- Vol. 22 (7) , 841-847
Abstract
Recent studies have demonstrated the important enzymatic, structural and regulatory roles of RNA in the cell. Here we present a post-transcriptional regulation system in Escherichia coli that uses RNA to both silence and activate gene expression. We inserted a complementary cis sequence directly upstream of the ribosome binding site in a target gene. Upon transcription, this cis-repressive sequence causes a stem-loop structure to form at the 5′–untranslated region of the mRNA. The stem-loop structure interferes with ribosome binding, silencing gene expression. A small noncoding RNA that is expressed in trans targets the cis-repressed RNA with high specificity, causing an alteration in the stem-loop structure that activates expression. Such engineered riboregulators may lend insight into mechanistic actions of endogenous RNA-based processes and could serve as scalable components of biological networks, able to function with any promoter or gene to directly control gene expression.Keywords
This publication has 48 references indexed in Scilit:
- Control of gene expression by a natural metabolite-responsive ribozymeNature, 2004
- Killing the messenger: short RNAs that silence gene expressionNature Reviews Molecular Cell Biology, 2003
- Engineered gene circuitsNature, 2002
- The antiquity of RNA-based evolutionNature, 2002
- Non–coding RNA genes and the modern RNA worldNature Reviews Genetics, 2001
- Antisense RNA regulation in prokaryotes: rapid RNA/RNA interaction facilitated by a general U-turn loop structureJournal of Molecular Biology, 1999
- The C. elegans heterochronic gene lin-4 encodes small RNAs with antisense complementarity to lin-14Cell, 1993
- In vitro selection of RNA molecules that bind specific ligandsNature, 1990
- Systematic Evolution of Ligands by Exponential Enrichment: RNA Ligands to Bacteriophage T4 DNA PolymeraseScience, 1990
- Amplification, mutation and selection of catalytic RNAGene, 1989