
pmid: 2096017
AbstractWe describe the generation of Dictyostelium discoideum cell lines that carry different suppressor †RNA genes. These genes were constructed by primer‐directed mutagenesis changing a †RNATrp(CCA) gene from D. discoideum to a †RNATrp(amber) gene and changing a †RNAGlu(UUC) gene from D. discoideum to a †RNAGlu(ochre) as well as a †RNAGlu(amber) gene. These genes were stably integrated into the D. discoideum genome together with a reporter gene. An actin 6::lacZ gene fusion carrying corresponding translational stop signals served as a reported. Active β‐galactosidase is expressed only in D. discoideum strains that contain, in addition to the reporter, a functional suppressor †RNA. Both amber suppressors are active in D. discoideum without interfering significantly with cell growth and development. We failed, however, to establish cell lines containing a functional †RNAGlu(ochre) suppressor. This may be due to the fact that nearly every message from D. discoideum known so far terminates with UAA. Therefore a †RNA capable of reading this termination codon may not be compatible with cell growth.
Base Sequence, Genes, Fungal, Molecular Sequence Data, Nucleic Acid Hybridization, Saccharomyces cerevisiae, Blotting, Northern, RNA, Transfer, Trp, Blotting, Southern, Phenotype, Gene Expression Regulation, Fungal, Mutagenesis, Site-Directed, Dictyostelium, Electrophoresis, Polyacrylamide Gel, Genes, Lethal, Genes, Suppressor, Plasmids
Base Sequence, Genes, Fungal, Molecular Sequence Data, Nucleic Acid Hybridization, Saccharomyces cerevisiae, Blotting, Northern, RNA, Transfer, Trp, Blotting, Southern, Phenotype, Gene Expression Regulation, Fungal, Mutagenesis, Site-Directed, Dictyostelium, Electrophoresis, Polyacrylamide Gel, Genes, Lethal, Genes, Suppressor, Plasmids
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