1. Expression of lexA targeted ribozyme in Escherichia coli BL-21 (DE3) cells
- Author
-
Ravindra Kumar, Ramesh S. Yadava, and Pramod Kumar Yadava
- Subjects
Isopropyl Thiogalactoside ,Hammerhead ribozyme ,Ultraviolet Rays ,viruses ,Clinical Biochemistry ,Biology ,Viral Proteins ,Bacterial Proteins ,Escherichia coli ,medicine ,T7 RNA polymerase ,RNA, Catalytic ,RNA, Messenger ,Cloning, Molecular ,SOS response ,Promoter Regions, Genetic ,Molecular Biology ,Serine Endopeptidases ,Ribozyme ,RNA ,DNA-Directed RNA Polymerases ,Gene Expression Regulation, Bacterial ,Cell Biology ,General Medicine ,biology.organism_classification ,Molecular biology ,biology.protein ,bacteria ,Mammalian CPEB3 ribozyme ,Repressor lexA ,VS ribozyme ,medicine.drug - Abstract
Coding sequences for a hammerhead ribozyme designed to cleave lexA mRNA in a targeted manner was cloned under phage T7 promoter and expressed in E. coli strain BL-21 (DE3) expressing T7 RNA polymerase under the control of IPTG-inducible lac UV-5 promoter. Ribozyme expression in vivo was demonstrated by RNase protection assay. Also, total RNA extracted from these transformed cells following induction by IPTG, displays site-specific cleavage of labeled lexA RNA in an in vitro reaction. The result demonstrates the active ribozyme in extracts of cell transformed with a recombinant cassette and goes beyond the earlier demonstration of the stability of in vitro synthesized ribozyme in cell extracts. The observed rise in lexA mRNA rules out any role for protease activity or resulting fragments of lexA protein in de-repression of RNA.
- Published
- 2005