Autogenous suppression of an opal mutation in the gene encoding peptide chain release factor 2
- PMID: 2236050
- PMCID: PMC54970
- DOI: 10.1073/pnas.87.21.8432
Autogenous suppression of an opal mutation in the gene encoding peptide chain release factor 2
Abstract
The peptide chain release factor 2 (RF2) gene, prfB, was cloned from Salmonella typhimurium by DNA hybridization using the Escherichia coli prfB probe. The nucleotide and amino acid sequences of prfB are 87.0% and 95.6% homologous between E. coli and S. typhimurium, respectively, including an in-frame premature UGA stop codon at position 26, the site of +1 frameshift for mature RF2 synthesis. The supK584 mutation, which had been isolated as a recessive UGA suppressor in S. typhimurium, caused an opal (UGA) substitution at amino acid position 144 in the prfB gene. Complementation, reversion, and gene fusion analyses led to the conclusion that supK is a S. typhimurium RF2 mutation and this opal RF2 mutation generates a UGA suppressor activity, presumably because of inefficient translation termination due to the reduced cellular level of RF2. In fact, suppression of the supK opal mutation results from a form of autogenous control of RF2 synthesis.
Similar articles
-
Chromosomal location and structure of the operon encoding peptide-chain-release factor 2 of Escherichia coli.Proc Natl Acad Sci U S A. 1988 Aug;85(15):5620-4. doi: 10.1073/pnas.85.15.5620. Proc Natl Acad Sci U S A. 1988. PMID: 2456575 Free PMC article.
-
Sequence and functional analysis of mutations in the gene encoding peptide-chain-release factor 2 of Escherichia coli.Biochimie. 1991 Dec;73(12):1509-16. doi: 10.1016/0300-9084(91)90185-4. Biochimie. 1991. PMID: 1805966
-
Rapid and precise mapping of the Escherichia coli release factor genes by two physical approaches.J Bacteriol. 1988 Oct;170(10):4537-41. doi: 10.1128/jb.170.10.4537-4541.1988. J Bacteriol. 1988. PMID: 3049538 Free PMC article.
-
The function, structure and regulation of E. coli peptide chain release factors.Biochimie. 1987 Oct;69(10):1031-41. doi: 10.1016/0300-9084(87)90003-4. Biochimie. 1987. PMID: 3126822 Review.
-
Recent advances in peptide chain termination.Mol Microbiol. 1990 Jun;4(6):861-5. doi: 10.1111/j.1365-2958.1990.tb00658.x. Mol Microbiol. 1990. PMID: 2215213 Free PMC article. Review.
Cited by
-
Poly(A)-binding protein acts in translation termination via eukaryotic release factor 3 interaction and does not influence [PSI(+)] propagation.Mol Cell Biol. 2002 May;22(10):3301-15. doi: 10.1128/MCB.22.10.3301-3315.2002. Mol Cell Biol. 2002. PMID: 11971964 Free PMC article.
-
Global analysis of translation termination in E. coli.PLoS Genet. 2017 Mar 16;13(3):e1006676. doi: 10.1371/journal.pgen.1006676. eCollection 2017 Mar. PLoS Genet. 2017. PMID: 28301469 Free PMC article.
-
Viable nonsense mutants for the essential gene SUP45 of Saccharomyces cerevisiae.BMC Mol Biol. 2003 Feb 10;4:2. doi: 10.1186/1471-2199-4-2. Epub 2003 Feb 10. BMC Mol Biol. 2003. PMID: 12589713 Free PMC article.
-
Sequence comparison of new prokaryotic and mitochondrial members of the polypeptide chain release factor family predicts a five-domain model for release factor structure.Nucleic Acids Res. 1992 Sep 11;20(17):4423-8. doi: 10.1093/nar/20.17.4423. Nucleic Acids Res. 1992. PMID: 1408743 Free PMC article.
-
Autoregulatory systems controlling translation factor expression: thermostat-like control of translational accuracy.RNA. 2010 Apr;16(4):655-63. doi: 10.1261/rna.1796210. Epub 2010 Feb 25. RNA. 2010. PMID: 20185543 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
Associated data
- Actions
LinkOut - more resources
Full Text Sources
Molecular Biology Databases