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. 1995 Feb 25;23(4):683–688. doi: 10.1093/nar/23.4.683

Decoding with the A:I wobble pair is inefficient.

J F Curran 1
PMCID: PMC306738  PMID: 7534909

Abstract

tRNAs with inosine (I) in the first position read three codons ending in U, C and A. However, A-ending codons read with I are rarely used. In Escherichia coli, CGA/U/C are all read solely by tRNAICGArg. CGU and CGC are very common codons, but CGA is very rare. Three independent in vivo assays show that translation of CGA is relatively inefficient. In the first, nine tandem CGA cause a strong rho-mediated polar effect on expression of a lacZ reporter gene. The inhibition is made more extreme by a mutation in ribosomal protein S12 (rpsL), which indicates that ribosomal binding by tRNAICGArg is slow and/or unstable in the CGA cluster. The second assay, in which codons are substituted for the regulatory UGA of the RF2 frameshift, confirms that aa-tRNA selection is slow and/or unstable at CGA. In the third assay, CGA is found to be a poor 5' context for amber suppression, which suggests that an A:I base pair in the P site can interfere with translation of a codon in the A site. Two possible errors, frameshifting and premature termination by RF2, are not significant causes for inefficiency at CGA. It is concluded that the A:I pair destabilizes codon:anticodon complexes during two successive ribosomal cycles, and it is suggested that these properties contribute to the rare usage of codons read with the A:I base pair.

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  1. Adamski F. M., Donly B. C., Tate W. P. Competition between frameshifting, termination and suppression at the frameshift site in the Escherichia coli release factor-2 mRNA. Nucleic Acids Res. 1993 Nov 11;21(22):5074–5078. doi: 10.1093/nar/21.22.5074. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Adhya S., Gottesman M. Control of transcription termination. Annu Rev Biochem. 1978;47:967–996. doi: 10.1146/annurev.bi.47.070178.004535. [DOI] [PubMed] [Google Scholar]
  3. Andachi Y., Yamao F., Muto A., Osawa S. Codon recognition patterns as deduced from sequences of the complete set of transfer RNA species in Mycoplasma capricolum. Resemblance to mitochondria. J Mol Biol. 1989 Sep 5;209(1):37–54. doi: 10.1016/0022-2836(89)90168-x. [DOI] [PubMed] [Google Scholar]
  4. Bennetzen J. L., Hall B. D. Codon selection in yeast. J Biol Chem. 1982 Mar 25;257(6):3026–3031. [PubMed] [Google Scholar]
  5. Bilgin N., Claesens F., Pahverk H., Ehrenberg M. Kinetic properties of Escherichia coli ribosomes with altered forms of S12. J Mol Biol. 1992 Apr 20;224(4):1011–1027. doi: 10.1016/0022-2836(92)90466-w. [DOI] [PubMed] [Google Scholar]
  6. Bohman K., Ruusala T., Jelenc P. C., Kurland C. G. Kinetic impairment of restrictive streptomycin-resistant ribosomes. Mol Gen Genet. 1984;198(2):90–99. doi: 10.1007/BF00328706. [DOI] [PubMed] [Google Scholar]
  7. Brown C. M., Dalphin M. E., Stockwell P. A., Tate W. P. The translational termination signal database. Nucleic Acids Res. 1993 Jul 1;21(13):3119–3123. doi: 10.1093/nar/21.13.3119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Brown C. M., Stockwell P. A., Dalphin M. E., Tate W. P. The translational termination signal database (TransTerm) now also includes initiation contexts. Nucleic Acids Res. 1994 Sep;22(17):3620–3624. doi: 10.1093/nar/22.17.3620. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Brown C. M., Stockwell P. A., Trotman C. N., Tate W. P. The signal for the termination of protein synthesis in procaryotes. Nucleic Acids Res. 1990 Apr 25;18(8):2079–2086. doi: 10.1093/nar/18.8.2079. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Buckingham R. H. Codon context. Experientia. 1990 Dec 1;46(11-12):1126–1133. doi: 10.1007/BF01936922. [DOI] [PubMed] [Google Scholar]
  11. Bulmer M. Codon usage and intragenic position. J Theor Biol. 1988 Jul 8;133(1):67–71. doi: 10.1016/s0022-5193(88)80024-9. [DOI] [PubMed] [Google Scholar]
  12. Bulmer M. The effect of context on synonymous codon usage in genes with low codon usage bias. Nucleic Acids Res. 1990 May 25;18(10):2869–2873. doi: 10.1093/nar/18.10.2869. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Carter P. W., Bartkus J. M., Calvo J. M. Transcription attenuation in Salmonella typhimurium: the significance of rare leucine codons in the leu leader. Proc Natl Acad Sci U S A. 1986 Nov;83(21):8127–8131. doi: 10.1073/pnas.83.21.8127. [DOI] [PMC free article] [PubMed] [Google Scholar]
  14. Chen G. F., Inouye M. Suppression of the negative effect of minor arginine codons on gene expression; preferential usage of minor codons within the first 25 codons of the Escherichia coli genes. Nucleic Acids Res. 1990 Mar 25;18(6):1465–1473. doi: 10.1093/nar/18.6.1465. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Crick F. H. Codon--anticodon pairing: the wobble hypothesis. J Mol Biol. 1966 Aug;19(2):548–555. doi: 10.1016/s0022-2836(66)80022-0. [DOI] [PubMed] [Google Scholar]
  16. Curran J. F., Gross B. L. Evidence that GHN phase bias does not constitute a framing code. J Mol Biol. 1994 Jan 7;235(1):389–395. doi: 10.1016/s0022-2836(05)80046-4. [DOI] [PubMed] [Google Scholar]
  17. Curran J. F., Yarus M. Base substitutions in the tRNA anticodon arm do not degrade the accuracy of reading frame maintenance. Proc Natl Acad Sci U S A. 1986 Sep;83(17):6538–6542. doi: 10.1073/pnas.83.17.6538. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Curran J. F., Yarus M. Rates of aminoacyl-tRNA selection at 29 sense codons in vivo. J Mol Biol. 1989 Sep 5;209(1):65–77. doi: 10.1016/0022-2836(89)90170-8. [DOI] [PubMed] [Google Scholar]
  19. Curran J. F., Yarus M. Use of tRNA suppressors to probe regulation of Escherichia coli release factor 2. J Mol Biol. 1988 Sep 5;203(1):75–83. doi: 10.1016/0022-2836(88)90092-7. [DOI] [PubMed] [Google Scholar]
  20. Das A., Court D., Adhya S. Isolation and characterization of conditional lethal mutants of Escherichia coli defective in transcription termination factor rho. Proc Natl Acad Sci U S A. 1976 Jun;73(6):1959–1963. doi: 10.1073/pnas.73.6.1959. [DOI] [PMC free article] [PubMed] [Google Scholar]
  21. Folley L. S., Yarus M. Codon contexts from weakly expressed genes reduce expression in vivo. J Mol Biol. 1989 Oct 5;209(3):359–378. doi: 10.1016/0022-2836(89)90003-x. [DOI] [PubMed] [Google Scholar]
  22. Gorini L. Ribosomal discrimination of tRNAs. Nat New Biol. 1971 Dec 29;234(52):261–264. doi: 10.1038/newbio234261a0. [DOI] [PubMed] [Google Scholar]
  23. Gouy M. Codon contexts in enterobacterial and coliphage genes. Mol Biol Evol. 1987 Jul;4(4):426–444. doi: 10.1093/oxfordjournals.molbev.a040450. [DOI] [PubMed] [Google Scholar]
  24. Gouy M., Gautier C. Codon usage in bacteria: correlation with gene expressivity. Nucleic Acids Res. 1982 Nov 25;10(22):7055–7074. doi: 10.1093/nar/10.22.7055. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Guillerez J., Gazeau M., Dreyfus M. In the Escherichia coli lacZ gene the spacing between the translating ribosomes is insensitive to the efficiency of translation initiation. Nucleic Acids Res. 1991 Dec 25;19(24):6743–6750. doi: 10.1093/nar/19.24.6743. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Hanai R., Wada A. Novel third-letter bias in Escherichia coli codons revealed by rigorous treatment of coding constraints. J Mol Biol. 1989 Jun 20;207(4):655–660. doi: 10.1016/0022-2836(89)90235-0. [DOI] [PubMed] [Google Scholar]
  27. Harms E., Umbarger H. E. Role of codon choice in the leader region of the ilvGMEDA operon of Serratia marcescens. J Bacteriol. 1987 Dec;169(12):5668–5677. doi: 10.1128/jb.169.12.5668-5677.1987. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Ikemura T. Correlation between the abundance of Escherichia coli transfer RNAs and the occurrence of the respective codons in its protein genes. J Mol Biol. 1981 Feb 15;146(1):1–21. doi: 10.1016/0022-2836(81)90363-6. [DOI] [PubMed] [Google Scholar]
  29. Kato M., Nishikawa K., Uritani M., Miyazaki M., Takemura S. The difference in the type of codon-anticodon base pairing at the ribosomal P-site is one of the determinants of the translational rate. J Biochem. 1990 Feb;107(2):242–247. doi: 10.1093/oxfordjournals.jbchem.a123033. [DOI] [PubMed] [Google Scholar]
  30. Komine Y., Adachi T., Inokuchi H., Ozeki H. Genomic organization and physical mapping of the transfer RNA genes in Escherichia coli K12. J Mol Biol. 1990 Apr 20;212(4):579–598. doi: 10.1016/0022-2836(90)90224-A. [DOI] [PubMed] [Google Scholar]
  31. Lim V. I., Venclovas C. Codon-anticodon pairing. A model for interacting codon-anticodon duplexes located at the ribosomal A- and P-sites. FEBS Lett. 1992 Nov 23;313(2):133–137. doi: 10.1016/0014-5793(92)81429-p. [DOI] [PubMed] [Google Scholar]
  32. Lim V., Venclovas C., Spirin A., Brimacombe R., Mitchell P., Müller F. How are tRNAs and mRNA arranged in the ribosome? An attempt to correlate the stereochemistry of the tRNA-mRNA interaction with constraints imposed by the ribosomal topography. Nucleic Acids Res. 1992 Jun 11;20(11):2627–2637. doi: 10.1093/nar/20.11.2627. [DOI] [PMC free article] [PubMed] [Google Scholar]
  33. McCormick J. R., Zengel J. M., Lindahl L. Correlation of translation efficiency with the decay of lacZ mRNA in Escherichia coli. J Mol Biol. 1994 Jun 24;239(5):608–622. doi: 10.1006/jmbi.1994.1403. [DOI] [PubMed] [Google Scholar]
  34. Miller J. H., Albertini A. M. Effects of surrounding sequence on the suppression of nonsense codons. J Mol Biol. 1983 Feb 15;164(1):59–71. doi: 10.1016/0022-2836(83)90087-6. [DOI] [PubMed] [Google Scholar]
  35. Munz P., Leupold U., Agris P., Kohli J. In vivo decoding rules in Schizosaccharomyces pombe are at variance with in vitro data. Nature. 1981 Nov 12;294(5837):187–188. doi: 10.1038/294187a0. [DOI] [PubMed] [Google Scholar]
  36. Nirenberg M., Leder P., Bernfield M., Brimacombe R., Trupin J., Rottman F., O'Neal C. RNA codewords and protein synthesis, VII. On the general nature of the RNA code. Proc Natl Acad Sci U S A. 1965 May;53(5):1161–1168. doi: 10.1073/pnas.53.5.1161. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Pedersen W. T., Curran J. F. Effects of the nucleotide 3' to an amber codon on ribosomal selection rates of suppressor tRNA and release factor-1. J Mol Biol. 1991 May 20;219(2):231–241. doi: 10.1016/0022-2836(91)90564-m. [DOI] [PubMed] [Google Scholar]
  38. Richardson J. P. Preventing the synthesis of unused transcripts by Rho factor. Cell. 1991 Mar 22;64(6):1047–1049. doi: 10.1016/0092-8674(91)90257-y. [DOI] [PubMed] [Google Scholar]
  39. Robinson M., Lilley R., Little S., Emtage J. S., Yarranton G., Stephens P., Millican A., Eaton M., Humphreys G. Codon usage can affect efficiency of translation of genes in Escherichia coli. Nucleic Acids Res. 1984 Sep 11;12(17):6663–6671. doi: 10.1093/nar/12.17.6663. [DOI] [PMC free article] [PubMed] [Google Scholar]
  40. Rosenberg A. H., Goldman E., Dunn J. J., Studier F. W., Zubay G. Effects of consecutive AGG codons on translation in Escherichia coli, demonstrated with a versatile codon test system. J Bacteriol. 1993 Feb;175(3):716–722. doi: 10.1128/jb.175.3.716-722.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. Ruteshouser E. C., Richardson J. P. Identification and characterization of transcription termination sites in the Escherichia coli lacZ gene. J Mol Biol. 1989 Jul 5;208(1):23–43. doi: 10.1016/0022-2836(89)90085-5. [DOI] [PubMed] [Google Scholar]
  42. Sharp P. M., Li W. H. The codon Adaptation Index--a measure of directional synonymous codon usage bias, and its potential applications. Nucleic Acids Res. 1987 Feb 11;15(3):1281–1295. doi: 10.1093/nar/15.3.1281. [DOI] [PMC free article] [PubMed] [Google Scholar]
  43. Shpaer E. G. Constraints on codon context in Escherichia coli genes. Their possible role in modulating the efficiency of translation. J Mol Biol. 1986 Apr 20;188(4):555–564. doi: 10.1016/s0022-2836(86)80005-5. [DOI] [PubMed] [Google Scholar]
  44. Sipley J., Goldman E. Increased ribosomal accuracy increases a programmed translational frameshift in Escherichia coli. Proc Natl Acad Sci U S A. 1993 Mar 15;90(6):2315–2319. doi: 10.1073/pnas.90.6.2315. [DOI] [PMC free article] [PubMed] [Google Scholar]
  45. Smith D., Yarus M. tRNA-tRNA interactions within cellular ribosomes. Proc Natl Acad Sci U S A. 1989 Jun;86(12):4397–4401. doi: 10.1073/pnas.86.12.4397. [DOI] [PMC free article] [PubMed] [Google Scholar]
  46. Spanjaard R. A., Chen K., Walker J. R., van Duin J. Frameshift suppression at tandem AGA and AGG codons by cloned tRNA genes: assigning a codon to argU tRNA and T4 tRNA(Arg). Nucleic Acids Res. 1990 Sep 11;18(17):5031–5036. doi: 10.1093/nar/18.17.5031. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Spanjaard R. A., van Duin J. Translation of the sequence AGG-AGG yields 50% ribosomal frameshift. Proc Natl Acad Sci U S A. 1988 Nov;85(21):7967–7971. doi: 10.1073/pnas.85.21.7967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Sprinzl M., Dank N., Nock S., Schön A. Compilation of tRNA sequences and sequences of tRNA genes. Nucleic Acids Res. 1991 Apr 25;19 (Suppl):2127–2171. doi: 10.1093/nar/19.suppl.2127. [DOI] [PMC free article] [PubMed] [Google Scholar]
  49. Stanssens P., Remaut E., Fiers W. Inefficient translation initiation causes premature transcription termination in the lacZ gene. Cell. 1986 Mar 14;44(5):711–718. doi: 10.1016/0092-8674(86)90837-8. [DOI] [PubMed] [Google Scholar]
  50. Stormo G. D., Schneider T. D., Gold L. Quantitative analysis of the relationship between nucleotide sequence and functional activity. Nucleic Acids Res. 1986 Aug 26;14(16):6661–6679. doi: 10.1093/nar/14.16.6661. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Suzuki T., Ueda T., Yokogawa T., Nishikawa K., Watanabe K. Characterization of serine and leucine tRNAs in an asporogenic yeast Candida cylindracea and evolutionary implications of genes for tRNA(Ser)CAG responsible for translation of a non-universal genetic code. Nucleic Acids Res. 1994 Jan 25;22(2):115–123. doi: 10.1093/nar/22.2.115. [DOI] [PMC free article] [PubMed] [Google Scholar]
  52. Söll D., Ohtsuka E., Jones D. S., Lohrmann R., Hayatsu H., Nishimura S., Khorana H. G. Studies on polynucleotides, XLIX. Stimulation of the binding of aminoacyl-sRNA's to ribosomes by ribotrinucleotides and a survey of codon assignments for 20 amino acids. Proc Natl Acad Sci U S A. 1965 Nov;54(5):1378–1385. doi: 10.1073/pnas.54.5.1378. [DOI] [PMC free article] [PubMed] [Google Scholar]
  53. Sørensen M. A., Pedersen S. Absolute in vivo translation rates of individual codons in Escherichia coli. The two glutamic acid codons GAA and GAG are translated with a threefold difference in rate. J Mol Biol. 1991 Nov 20;222(2):265–280. doi: 10.1016/0022-2836(91)90211-n. [DOI] [PubMed] [Google Scholar]
  54. Thompson R. C., Dix D. B., Gerson R. B., Karim A. M. Effect of Mg2+ concentration, polyamines, streptomycin, and mutations in ribosomal proteins on the accuracy of the two-step selection of aminoacyl-tRNAs in protein biosynthesis. J Biol Chem. 1981 Jul 10;256(13):6676–6681. [PubMed] [Google Scholar]
  55. VOGEL H. J., BONNER D. M. Acetylornithinase of Escherichia coli: partial purification and some properties. J Biol Chem. 1956 Jan;218(1):97–106. [PubMed] [Google Scholar]
  56. Varenne S., Lazdunski C. Effect of distribution of unfavourable codons on the maximum rate of gene expression by an heterologous organism. J Theor Biol. 1986 May 7;120(1):99–110. doi: 10.1016/s0022-5193(86)80020-0. [DOI] [PubMed] [Google Scholar]
  57. Yarus M., Folley L. S. Sense codons are found in specific contexts. J Mol Biol. 1985 Apr 20;182(4):529–540. doi: 10.1016/0022-2836(85)90239-6. [DOI] [PubMed] [Google Scholar]
  58. Yarus M., McMillan C., 3rd, Cline S., Bradley D., Snyder M. Construction of a composite tRNA gene by anticodon loop transplant. Proc Natl Acad Sci U S A. 1980 Sep;77(9):5092–5096. doi: 10.1073/pnas.77.9.5092. [DOI] [PMC free article] [PubMed] [Google Scholar]

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