| Literature DB >> 23595083 |
Athanasios Saragliadis1, Stefanie S Krajewski, Charlotte Rehm, Franz Narberhaus, Jörg S Hartig.
Abstract
Synthetic biology approaches often combine natural building blocks to generate new cellular activities. Here, we make use of two RNA elements to design a regulatory device with novel functionality. The system is based on a hammerhead ribozyme (HHR) that cleaves itself to generate a liberated ribosome-binding site and, thus, permits expression of a downstream gene. We connected a temperature-responsive RNA hairpin to the HHR and, thus, generated a temperature-controlled ribozyme that we call thermozyme. Specifically, a Salmonella RNA thermometer (RNAT) known to modulate small heat shock gene expression by temperature-controlled base-pairing and melting was fused to the ribozyme. Following an in vivo screening approach, we isolated two functional thermozymes. In vivo expression studies and in vitro structure probing experiments support a mechanism in which rising temperatures melt the thermometer structure impairing the self-cleavage reaction of the ribozyme. Since RNA cleavage is necessary to liberate the RBS, these engineered thermozymes shut off gene expression in response to a temperature increase and, thus, act in a reverse manner as the natural RNAT. Our results clearly emphasize the highly modular nature and biotechnological potential of ribozyme-based RNA thermometers.Entities:
Keywords: RNA thermometer; gene expression; hammerhead ribozyme; regulatory RNA; riboswitch; temperature
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Year: 2013 PMID: 23595083 PMCID: PMC4111729 DOI: 10.4161/rna.24482
Source DB: PubMed Journal: RNA Biol ISSN: 1547-6286 Impact factor: 4.652