Skip to main content
Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1988 Jun;85(12):4162–4165. doi: 10.1073/pnas.85.12.4162

Mutant 16S ribosomal RNA: a codon-specific translational suppressor.

E J Murgola 1, K A Hijazi 1, H U Göringer 1, A E Dahlberg 1
PMCID: PMC280386  PMID: 3288986

Abstract

We have isolated an unusual codon-specific translational suppressor in Escherichia coli. The suppressor resulted from a spontaneous mutation in a chromosomal gene during a selection for suppressors of the auxotrophic nonsense mutation trpA(UGA211). The suppressor allows readthrough of UGA mutations at two positions in trpA and at two sites in bacteriophage T4. It does not, however, suppress amber (UAG) or ochre (UAA) mutations that were tested in both genomes, some of which were at the same positions as the suppressible UGA mutations. The suppressor also does not allow mistranslation of the UGA-related trpA missense mutations UGG at positions 211 and 234, AGA at 211 and 234, CGA at 211, or UGU and UGC at 234. The suppressor mutation was mapped by genetic procedures to position 89 on the E. coli genetic map. Localization of the suppressor mutation to rrnB was achieved by cloning it in the low-copy-number plasmid pEJM007 by in vivo recombination from the chromosome. Recloning in bacteriophage M13 and subsequent DNA sequence analysis allowed the identification of the suppressor mutation as a deletion of the cytidylic acid residue at nucleotide position 1054 of the 16S ribosomal RNA. The mutant EcoRI-Xba I fragment from the suppressor gene was recloned, from M13, in an otherwise wild-type rrnB in the plasmid pEJM007, and UGA suppression was examined. The UGA-suppressing activity of the reconstructed suppressor-containing pEJM007 was indistinguishable from that of the original recombinant suppressor-containing plasmid. This result demonstrates that the C1054 deletion in 16S rRNA is both necessary and sufficient for UGA suppression. The existence of this mutant suggests an important role for rRNA in codon recognition, at least for accurate polypeptide chain termination.

Full text

PDF
4162

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Andersson D. I., Bohman K., Isaksson L. A., Kurland C. G. Translation rates and misreading characteristics of rpsD mutants in Escherichia coli. Mol Gen Genet. 1982;187(3):467–472. doi: 10.1007/BF00332630. [DOI] [PubMed] [Google Scholar]
  2. Bachmann B. J. Linkage map of Escherichia coli K-12, edition 7. Microbiol Rev. 1983 Jun;47(2):180–230. doi: 10.1128/mr.47.2.180-230.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Benzer S., Champe S. P. AMBIVALENT rII MUTANTS OF PHAGE T4. Proc Natl Acad Sci U S A. 1961 Jul;47(7):1025–1038. doi: 10.1073/pnas.47.7.1025. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Eustice D. C., Wakem L. P., Wilhelm J. M., Sherman F. Altered 40 S ribosomal subunits in omnipotent suppressors of yeast. J Mol Biol. 1986 Mar 20;188(2):207–214. doi: 10.1016/0022-2836(86)90305-0. [DOI] [PubMed] [Google Scholar]
  5. Fox T. D., Staempfli S. Suppressor of yeast mitochondrial ochre mutations that maps in or near the 15S ribosomal RNA gene of mtDNA. Proc Natl Acad Sci U S A. 1982 Mar;79(5):1583–1587. doi: 10.1073/pnas.79.5.1583. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Gorini L. Informational suppression. Annu Rev Genet. 1970;4:107–134. doi: 10.1146/annurev.ge.04.120170.000543. [DOI] [PubMed] [Google Scholar]
  7. Gutell R. R., Weiser B., Woese C. R., Noller H. F. Comparative anatomy of 16-S-like ribosomal RNA. Prog Nucleic Acid Res Mol Biol. 1985;32:155–216. doi: 10.1016/s0079-6603(08)60348-7. [DOI] [PubMed] [Google Scholar]
  8. Hui A., de Boer H. A. Specialized ribosome system: preferential translation of a single mRNA species by a subpopulation of mutated ribosomes in Escherichia coli. Proc Natl Acad Sci U S A. 1987 Jul;84(14):4762–4766. doi: 10.1073/pnas.84.14.4762. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Inokuchi H., Hoben P., Yamao F., Ozeki H., Söll D. Transfer RNA mischarging mediated by a mutant Escherichia coli glutaminyl-tRNA synthetase. Proc Natl Acad Sci U S A. 1984 Aug;81(16):5076–5080. doi: 10.1073/pnas.81.16.5076. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Jacob W. F., Santer M., Dahlberg A. E. A single base change in the Shine-Dalgarno region of 16S rRNA of Escherichia coli affects translation of many proteins. Proc Natl Acad Sci U S A. 1987 Jul;84(14):4757–4761. doi: 10.1073/pnas.84.14.4757. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Kirsebom L. A., Isaksson L. A. Involvement of ribosomal protein L7/L12 in control of translational accuracy. Proc Natl Acad Sci U S A. 1985 Feb;82(3):717–721. doi: 10.1073/pnas.82.3.717. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Moazed D., Noller H. F. Interaction of antibiotics with functional sites in 16S ribosomal RNA. Nature. 1987 Jun 4;327(6121):389–394. doi: 10.1038/327389a0. [DOI] [PubMed] [Google Scholar]
  13. Moazed D., Stern S., Noller H. F. Rapid chemical probing of conformation in 16 S ribosomal RNA and 30 S ribosomal subunits using primer extension. J Mol Biol. 1986 Feb 5;187(3):399–416. doi: 10.1016/0022-2836(86)90441-9. [DOI] [PubMed] [Google Scholar]
  14. Murgola E. J., Childress J. R. Suppressors of a UGG missense mutation in Escherichia coli. J Bacteriol. 1980 Jul;143(1):285–292. doi: 10.1128/jb.143.1.285-292.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Murgola E. J., Hijazi K. A. Selection for new codons corresponding to position 234 of the tryptophan synthetase alpha chain of Escherichia coli. Mol Gen Genet. 1983;191(1):132–137. doi: 10.1007/BF00330900. [DOI] [PubMed] [Google Scholar]
  16. Murgola E. J. Restricted wobble in UGA codon recognition by glycine tRNA suppressors of UGG. J Mol Biol. 1981 Jun 15;149(1):1–13. doi: 10.1016/0022-2836(81)90257-6. [DOI] [PubMed] [Google Scholar]
  17. Murgola E. J., Yanofsky C. Structural interactions between amino acid residues at positions 22 and 211 in the tryptophan synthetase alpha chain of Escherichia coli. J Bacteriol. 1974 Feb;117(2):444–448. doi: 10.1128/jb.117.2.444-448.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Murgola E. J. tRNA, suppression, and the code. Annu Rev Genet. 1985;19:57–80. doi: 10.1146/annurev.ge.19.120185.000421. [DOI] [PubMed] [Google Scholar]
  19. Noller H. F. Structure of ribosomal RNA. Annu Rev Biochem. 1984;53:119–162. doi: 10.1146/annurev.bi.53.070184.001003. [DOI] [PubMed] [Google Scholar]
  20. Reeves R. H., Roth J. R. Transfer ribonucleic acid methylase deficiency found in UGA supressor strains. J Bacteriol. 1975 Oct;124(1):332–340. doi: 10.1128/jb.124.1.332-340.1975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Sanger F., Nicklen S., Coulson A. R. DNA sequencing with chain-terminating inhibitors. Proc Natl Acad Sci U S A. 1977 Dec;74(12):5463–5467. doi: 10.1073/pnas.74.12.5463. [DOI] [PMC free article] [PubMed] [Google Scholar]
  22. Steen R., Jemiolo D. K., Skinner R. H., Dunn J. J., Dahlberg A. E. Expression of plasmid-coded mutant ribosomal RNA in E. coli: choice of plasmid vectors and gene expression systems. Prog Nucleic Acid Res Mol Biol. 1986;33:1–18. doi: 10.1016/s0079-6603(08)60018-5. [DOI] [PubMed] [Google Scholar]
  23. Weiss-Brummer B., Sakai H., Kaudewitz F. A mitochondrial frameshift-suppressor (+1) [corrected] of the yeast S. cerevisiae maps in the mitochondrial 15S rRNA locus. Curr Genet. 1987;11(4):295–301. doi: 10.1007/BF00355403. [DOI] [PubMed] [Google Scholar]
  24. YANOFSKY C., HELINSKI D. R., MALING B. D. The effects of mutation on the composition and properties of the A protein of Escherichia coli tryptohan synthetase. Cold Spring Harb Symp Quant Biol. 1961;26:11–24. doi: 10.1101/sqb.1961.026.01.006. [DOI] [PubMed] [Google Scholar]
  25. YANOFSKY C., LAWRENCE P. S. Gene action. Annu Rev Microbiol. 1960;14:311–340. doi: 10.1146/annurev.mi.14.100160.001523. [DOI] [PubMed] [Google Scholar]
  26. Yamao F., Muto A., Kawauchi Y., Iwami M., Iwagami S., Azumi Y., Osawa S. UGA is read as tryptophan in Mycoplasma capricolum. Proc Natl Acad Sci U S A. 1985 Apr;82(8):2306–2309. doi: 10.1073/pnas.82.8.2306. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Proceedings of the National Academy of Sciences of the United States of America are provided here courtesy of National Academy of Sciences

RESOURCES