Abstract
We have used a modified intron-containing tRNA(Pro(UGG) gene (tRNA(ProM), derived from the Saccharomyces cerevisiae tRNA(Pro(UGG) gene, as a reporter to measure in vivo transcription from a halophilic archaeon promoter. Coupling of the yeast tRNA(ProM) gene to the Haloferax volcanii tRNA(Lys) promoter on the H. volcanii plasmid pWL201 led to the production of a single stable transcript that was readily quantitated by Northern (RNA) blot analysis. Comparison of tRNA(ProM) RNA production from constructs containing the wild-type tRNA(Lys) promoter and those containing mutant tRNA(Lys) promoters demonstrated that this assay system can be used to measure expression from strong and weak promoters.
MeSH Terms
Base Sequence
DNA, Bacterial/genetics
Genes, Bacterial
Genes, Reporter
Halobacteriales/genetics
Molecular Sequence Data
Promoter Regions, Genetic
RNA, Transfer, Pro/genetics
Saccharomyces cerevisiae/genetics
Transcription, Genetic
Chemicals
DNA, Bacterial
RNA, Transfer, Pro
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Palmer J R
Department of Microbiology, Ohio State University, Columbus 43210.
Daniels C J
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