Abstract
Abstract
Background
Bioinformatic genome surveys indicate that self-cleaving ribonucleic acids (ribozymes) appear to be widespread among all domains of life, although the functions of only a small number have been validated by biochemical methods. Alternatively, cell-based reporter gene assays can be used to validate ribozyme function. However, reporter activity can be confounded by phenomena unrelated to ribozyme-mediated cleavage of RNA.
Results
We established a ribozyme reporter system in Escherichia coli in which a significant reduction of reporter activity is manifest when an active ribozyme sequence is fused to the reporter gene and the expression of a foreign Bacillus subtilis RNaseJ1 5′ exonuclease is induced from a chromosomally-integrated gene in the same cell.
Conclusions
The reporter system could be useful for validating ribozyme function in candidate sequences identified from bioinformatics.
Funder
Thailand Research Fund
National Science and Technology Development Agency
Publisher
Springer Science and Business Media LLC
Subject
Cell Biology,Molecular Biology