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
. 1990 Dec;87(23):9260–9264. doi: 10.1073/pnas.87.23.9260

Nucleotides that determine Escherichia coli tRNA(Arg) and tRNA(Lys) acceptor identities revealed by analyses of mutant opal and amber suppressor tRNAs.

W H McClain 1, K Foss 1, R A Jenkins 1, J Schneider 1
PMCID: PMC55144  PMID: 2251270

Abstract

We have constructed an opal suppressor system in Escherichia coli to complement an existing amber suppressor system to study the structural basis of tRNA acceptor identity, particularly the role of middle anticodon nucleotide at position 35. The opal suppressor tRNA contains a UCA anticodon and the mRNA of the suppressed protein (which is easily purified and sequenced) contains a UGA nonsense triplet. Opal suppressor tRNAs of two tRNA(Arg) isoacceptor sequences each gave arginine in the suppressed protein, while the corresponding amber suppressors with U35 in their CUA anticodons each gave arginine plus a second amino acid in the suppressed protein. Since C35 but not U35 is present in the anticodon of wild-type tRNA(Arg) molecules, while the first anticodon position contains either C34 or U34, these results establish that C35 contributes to tRNA(Arg) acceptor identity. Initial characterizations of opal suppressor tRNA(Arg) mutants by suppression efficiency measurements suggest that the fourth nucleotide from the 3' end of tRNA(Arg) (A73 or G73 in different isoacceptors) also contributes to tRNA(Arg) acceptor identity. Wild-type and mutant versions of opal and amber tRNA(Lys) suppressors were examined, revealing that U35 and A73 are important determinants of tRNA(Lys) acceptor identity. Several possibilities are discussed for the general significance of having tRNA acceptor identity in the same positions in different tRNA acceptor types, as exemplified by positions 35 and 73 in tRNA(Arg) and tRNA(Lys).

Full text

PDF
9260

Selected References

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

  1. Atilgan T., Nicholas H. B., Jr, McClain W. H. A statistical method for correlating tRNA sequence with amino acid specificity. Nucleic Acids Res. 1986 Jan 10;14(1):375–380. doi: 10.1093/nar/14.1.375. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Bare L. A., Uhlenbeck O. C. Specific substitution into the anticodon loop of yeast tyrosine transfer RNA. Biochemistry. 1986 Sep 23;25(19):5825–5830. doi: 10.1021/bi00367a072. [DOI] [PubMed] [Google Scholar]
  3. Chakraburtty K. Effect of sodium bisulfite modification on the arginine acceptance of E. coli tRNA Arg. Nucleic Acids Res. 1975 Oct;2(10):1793–1804. doi: 10.1093/nar/2.10.1793. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Chattapadhyay R., Pelka H., Schulman L. H. Initiation of in vivo protein synthesis with non-methionine amino acids. Biochemistry. 1990 May 8;29(18):4263–4268. doi: 10.1021/bi00470a001. [DOI] [PubMed] [Google Scholar]
  5. Crothers D. M., Seno T., Söll G. Is there a discriminator site in transfer RNA? Proc Natl Acad Sci U S A. 1972 Oct;69(10):3063–3067. doi: 10.1073/pnas.69.10.3063. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Eriani G., Delarue M., Poch O., Gangloff J., Moras D. Partition of tRNA synthetases into two classes based on mutually exclusive sets of sequence motifs. Nature. 1990 Sep 13;347(6289):203–206. doi: 10.1038/347203a0. [DOI] [PubMed] [Google Scholar]
  7. Francklyn C., Schimmel P. Aminoacylation of RNA minihelices with alanine. Nature. 1989 Feb 2;337(6206):478–481. doi: 10.1038/337478a0. [DOI] [PubMed] [Google Scholar]
  8. Guthrie C., Seidman J. G., Altman S., Barrell B. G., Smith J. D., McClain W. H. Identification of tRNA precursor molecules made by phage T4. Nat New Biol. 1973 Nov 7;246(149):6–11. doi: 10.1038/newbio246006a0. [DOI] [PubMed] [Google Scholar]
  9. Hasegawa T., Himeno H., Ishikura H., Shimizu M. Discriminator base of tRNA(Asp) is involved in amino acid acceptor activity. Biochem Biophys Res Commun. 1989 Sep 29;163(3):1534–1538. doi: 10.1016/0006-291x(89)91154-6. [DOI] [PubMed] [Google Scholar]
  10. Himeno H., Hasegawa T., Ueda T., Watanabe K., Miura K., Shimizu M. Role of the extra G-C pair at the end of the acceptor stem of tRNA(His) in aminoacylation. Nucleic Acids Res. 1989 Oct 11;17(19):7855–7863. doi: 10.1093/nar/17.19.7855. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Hooper M. L., Russell R. L., Smith J. D. Mischarging in mutant tyrosine transfer RNAs. FEBS Lett. 1972 Apr 15;22(1):149–155. doi: 10.1016/0014-5793(72)80241-2. [DOI] [PubMed] [Google Scholar]
  12. Hou Y. M., Schimmel P. A simple structural feature is a major determinant of the identity of a transfer RNA. Nature. 1988 May 12;333(6169):140–145. doi: 10.1038/333140a0. [DOI] [PubMed] [Google Scholar]
  13. Kern D., Giegé R., Ebel J. P. Incorrect aminoacylatins catalysed by the phenylalanyl-and valyl-tRNA synthetases from yeast. Eur J Biochem. 1972 Nov 21;31(1):148–155. doi: 10.1111/j.1432-1033.1972.tb02513.x. [DOI] [PubMed] [Google Scholar]
  14. Kisselev L. L. The role of the anticodon in recognition of tRNA by aminoacyl-tRNA synthetases. Prog Nucleic Acid Res Mol Biol. 1985;32:237–266. doi: 10.1016/s0079-6603(08)60350-5. [DOI] [PubMed] [Google Scholar]
  15. Klug A., Ladner J., Robertus J. D. The structural geometry of co-ordinated base changes in transfer RNA. J Mol Biol. 1974 Nov 5;89(3):511–516. doi: 10.1016/0022-2836(74)90480-x. [DOI] [PubMed] [Google Scholar]
  16. Knowlton R. G., Yarus M. Discrimination between aminoacyl groups on su+ 7 tRNA by elongation factor Tu. J Mol Biol. 1980 Jun 5;139(4):721–732. doi: 10.1016/0022-2836(80)90057-1. [DOI] [PubMed] [Google Scholar]
  17. Labouze E., Bedouelle H. Structural and kinetic bases for the recognition of tRNATyr by tyrosyl-tRNA synthetase. J Mol Biol. 1989 Feb 20;205(4):729–735. doi: 10.1016/0022-2836(89)90317-3. [DOI] [PubMed] [Google Scholar]
  18. Ladner J. E., Jack A., Robertus J. D., Brown R. S., Rhodes D., Clark B. F., Klug A. Structure of yeast phenylalanine transfer RNA at 2.5 A resolution. Proc Natl Acad Sci U S A. 1975 Nov;72(11):4414–4418. doi: 10.1073/pnas.72.11.4414. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. McClain W. H., Chen Y. M., Foss K., Schneider J. Association of transfer RNA acceptor identity with a helical irregularity. Science. 1988 Dec 23;242(4886):1681–1684. doi: 10.1126/science.2462282. [DOI] [PubMed] [Google Scholar]
  20. McClain W. H., Foss K. Changing the acceptor identity of a transfer RNA by altering nucleotides in a "variable pocket". Science. 1988 Sep 30;241(4874):1804–1807. doi: 10.1126/science.2459773. [DOI] [PubMed] [Google Scholar]
  21. McClain W. H., Foss K. Changing the identity of a tRNA by introducing a G-U wobble pair near the 3' acceptor end. Science. 1988 May 6;240(4853):793–796. doi: 10.1126/science.2452483. [DOI] [PubMed] [Google Scholar]
  22. McClain W. H., Foss K. Nucleotides that contribute to the identity of Escherichia coli tRNA(Phe). J Mol Biol. 1988 Aug 20;202(4):697–709. doi: 10.1016/0022-2836(88)90551-7. [DOI] [PubMed] [Google Scholar]
  23. McClain W. H., Nicholas H. B., Jr Differences between transfer RNA molecules. J Mol Biol. 1987 Apr 20;194(4):635–642. doi: 10.1016/0022-2836(87)90240-3. [DOI] [PubMed] [Google Scholar]
  24. 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]
  25. Miller P. S., McParland K. B., Jayaraman K., Ts'o P. O. Biochemical and biological effects of nonionic nucleic acid methylphosphonates. Biochemistry. 1981 Mar 31;20(7):1874–1880. doi: 10.1021/bi00510a024. [DOI] [PubMed] [Google Scholar]
  26. Moras D., Lorber B., Romby P., Ebel J. P., Giegé R., Lewit-Bentley A., Roth M. Yeast tRNAAsp-aspartyl-tRNA synthetase: the crystalline complex. J Biomol Struct Dyn. 1983 Oct;1(1):209–223. doi: 10.1080/07391102.1983.10507435. [DOI] [PubMed] [Google Scholar]
  27. Muramatsu T., Nishikawa K., Nemoto F., Kuchino Y., Nishimura S., Miyazawa T., Yokoyama S. Codon and amino-acid specificities of a transfer RNA are both converted by a single post-transcriptional modification. Nature. 1988 Nov 10;336(6195):179–181. doi: 10.1038/336179a0. [DOI] [PubMed] [Google Scholar]
  28. 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]
  29. Nicholas H. B., Jr, Graves S. B. Clustering of transfer RNAs by cell type and amino acid specificity. J Mol Biol. 1983 Dec 5;171(2):111–118. doi: 10.1016/s0022-2836(83)80348-9. [DOI] [PubMed] [Google Scholar]
  30. Normanly J., Kleina L. G., Masson J. M., Abelson J., Miller J. H. Construction of Escherichia coli amber suppressor tRNA genes. III. Determination of tRNA specificity. J Mol Biol. 1990 Jun 20;213(4):719–726. doi: 10.1016/S0022-2836(05)80258-X. [DOI] [PubMed] [Google Scholar]
  31. Normanly J., Ogden R. C., Horvath S. J., Abelson J. Changing the identity of a transfer RNA. Nature. 1986 May 15;321(6067):213–219. doi: 10.1038/321213a0. [DOI] [PubMed] [Google Scholar]
  32. Perona J. J., Swanson R. N., Rould M. A., Steitz T. A., Söll D. Structural basis for misaminoacylation by mutant E. coli glutaminyl-tRNA synthetase enzymes. Science. 1989 Dec 1;246(4934):1152–1154. doi: 10.1126/science.2686030. [DOI] [PubMed] [Google Scholar]
  33. Perret V., Garcia A., Grosjean H., Ebel J. P., Florentz C., Giegé R. Relaxation of a transfer RNA specificity by removal of modified nucleotides. Nature. 1990 Apr 19;344(6268):787–789. doi: 10.1038/344787a0. [DOI] [PubMed] [Google Scholar]
  34. Prather N. E., Murgola E. J., Mims B. H. Nucleotide substitution in the amino acid acceptor stem of lysine transfer RNA causes missense suppression. J Mol Biol. 1984 Jan 15;172(2):177–184. doi: 10.1016/s0022-2836(84)80036-4. [DOI] [PubMed] [Google Scholar]
  35. Quigley G. J., Wang A. H., Seeman N. C., Suddath F. L., Rich A., Sussman J. L., Kim S. H. Hydrogen bonding in yeast phenylalanine transfer RNA. Proc Natl Acad Sci U S A. 1975 Dec;72(12):4866–4870. doi: 10.1073/pnas.72.12.4866. [DOI] [PMC free article] [PubMed] [Google Scholar]
  36. Rogers M. J., Söll D. Discrimination between glutaminyl-tRNA synthetase and seryl-tRNA synthetase involves nucleotides in the acceptor helix of tRNA. Proc Natl Acad Sci U S A. 1988 Sep;85(18):6627–6631. doi: 10.1073/pnas.85.18.6627. [DOI] [PMC free article] [PubMed] [Google Scholar]
  37. Romby P., Moras D., Bergdoll M., Dumas P., Vlassov V. V., Westhof E., Ebel J. P., Giegé R. Yeast tRNAAsp tertiary structure in solution and areas of interaction of the tRNA with aspartyl-tRNA synthetase. A comparative study of the yeast phenylalanine system by phosphate alkylation experiments with ethylnitrosourea. J Mol Biol. 1985 Aug 5;184(3):455–471. doi: 10.1016/0022-2836(85)90294-3. [DOI] [PubMed] [Google Scholar]
  38. Rould M. A., Perona J. J., Söll D., Steitz T. A. Structure of E. coli glutaminyl-tRNA synthetase complexed with tRNA(Gln) and ATP at 2.8 A resolution. Science. 1989 Dec 1;246(4934):1135–1142. doi: 10.1126/science.2479982. [DOI] [PubMed] [Google Scholar]
  39. Sampson J. R., DiRenzo A. B., Behlen L. S., Uhlenbeck O. C. Role of the tertiary nucleotides in the interaction of yeast phenylalanine tRNA with its cognate synthetase. Biochemistry. 1990 Mar 13;29(10):2523–2532. doi: 10.1021/bi00462a014. [DOI] [PubMed] [Google Scholar]
  40. Saneyoshi M., Nishimura S. Selective inactivation of amino acid acceptor and ribosome-binding activities of Escherichia coli tRNA by modification with cyanogen bromide. Biochim Biophys Acta. 1971 Aug 12;246(1):123–131. doi: 10.1016/0005-2787(71)90077-3. [DOI] [PubMed] [Google Scholar]
  41. Schulman L. H., Chambers R. W. Transfer RNA, II. A structural basis for alanine acceptor activity. Proc Natl Acad Sci U S A. 1968 Sep;61(1):308–315. doi: 10.1073/pnas.61.1.308. [DOI] [PMC free article] [PubMed] [Google Scholar]
  42. Schulman L. H., Pelka H. Anticodon switching changes the identity of methionine and valine transfer RNAs. Science. 1988 Nov 4;242(4879):765–768. doi: 10.1126/science.3055296. [DOI] [PubMed] [Google Scholar]
  43. Schulman L. H., Pelka H. The anticodon contains a major element of the identity of arginine transfer RNAs. Science. 1989 Dec 22;246(4937):1595–1597. doi: 10.1126/science.2688091. [DOI] [PubMed] [Google Scholar]
  44. Seong B. L., Lee C. P., RajBhandary U. L. Suppression of amber codons in vivo as evidence that mutants derived from Escherichia coli initiator tRNA can act at the step of elongation in protein synthesis. J Biol Chem. 1989 Apr 15;264(11):6504–6508. [PubMed] [Google Scholar]
  45. Shi J. P., Francklyn C., Hill K., Schimmel P. A nucleotide that enhances the charging of RNA minihelix sequence variants with alanine. Biochemistry. 1990 Apr 17;29(15):3621–3626. doi: 10.1021/bi00467a005. [DOI] [PubMed] [Google Scholar]
  46. Shimura Y., Aono H., Ozeki H., Sarabhai A., Lamfrom H., Abelson J. Mutant tyrosine tRNA of altered amino acid specificity. FEBS Lett. 1972 Apr 15;22(1):144–148. doi: 10.1016/0014-5793(72)80240-0. [DOI] [PubMed] [Google Scholar]
  47. Sprinzl M., Hartmann T., Weber J., Blank J., Zeidler R. Compilation of tRNA sequences and sequences of tRNA genes. Nucleic Acids Res. 1989;17 (Suppl):r1–172. doi: 10.1093/nar/17.suppl.r1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Swanson R., Hoben P., Sumner-Smith M., Uemura H., Watson L., Söll D. Accuracy of in vivo aminoacylation requires proper balance of tRNA and aminoacyl-tRNA synthetase. Science. 1988 Dec 16;242(4885):1548–1551. doi: 10.1126/science.3144042. [DOI] [PubMed] [Google Scholar]
  49. Theobald A., Springer M., Grunberg-Manago M., Ebel J. P., Giege R. Tertiary structure of Escherichia coli tRNA(3Thr) in solution and interaction of this tRNA with the cognate threonyl-tRNA synthetase. Eur J Biochem. 1988 Aug 15;175(3):511–524. doi: 10.1111/j.1432-1033.1988.tb14223.x. [DOI] [PubMed] [Google Scholar]
  50. Uemura H., Imai M., Ohtsuka E., Ikehara M., Söll D. E. coli initiator tRNA analogs with different nucleotides in the discriminator base position. Nucleic Acids Res. 1982 Oct 25;10(20):6531–6539. doi: 10.1093/nar/10.20.6531. [DOI] [PMC free article] [PubMed] [Google Scholar]
  51. Vlassov V. V., Kern D., Romby P., Giegé R., Ebel J. P. Interaction of tRNAPhe and tRNAVal with aminoacyl-tRNA synthetases. A chemical modification study. Eur J Biochem. 1983 May 16;132(3):537–544. doi: 10.1111/j.1432-1033.1983.tb07395.x. [DOI] [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