Abstract
The alpha-sarcin loop of large subunit rRNAs is one of the sites of interaction of elongation factors with the ribosome, and the target of the cytotoxins alpha-sarcin and ricin. Using a genetic selection for increased frameshifting in a reporter gene, we have isolated a C --> U mutation at position 2666 in the alpha-sarcin loop. In the NMR-derived structure of the loop, bases equivalent to 2666 and 2654 are paired via a non-canonical base pairing interaction. Each of the three base substitutions at C2666 and A2654 was constructed by site-directed mutagenesis of a plasmid borne copy of the rrnB operon of Escherichia coli. Only the C2666 --> U and A2654 --> G mutations that resulted in the formation of canonical A-U and C-G base pairs respectively, increased the levels of stop codon readthrough and frameshifting. The effects of different base pair combinations at positions 2666 and 2654 on ribosome function were then tested by constructing and analyzing all possible base combinations at these sites. All A --> G base substitution mutations at position 2654 and C --> U substitutions at position 2666 increased the levels of translational errors. However, these effects were greatest when G2654 and U2666 had the potential to engage in standard Watson-Crick base pairing interactions. These data indicate that base identity as well as base pairing interactions are important for the function of this essential component of the large subunit rRNA.
Full Text
The Full Text of this article is available as a PDF (63.8 KB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Aagaard C., Rosendahl G., Dam M., Powers T., Douthwaite S. Specific structural probing of plasmid-coded ribosomal RNAs from Escherichia coli. Biochimie. 1991 Dec;73(12):1439–1444. doi: 10.1016/0300-9084(91)90176-2. [DOI] [PubMed] [Google Scholar]
- Bilgin N., Ehrenberg M. Mutations in 23 S ribosomal RNA perturb transfer RNA selection and can lead to streptomycin dependence. J Mol Biol. 1994 Jan 21;235(3):813–824. doi: 10.1006/jmbi.1994.1041. [DOI] [PubMed] [Google Scholar]
- Chernoff Y. O., Newnam G. P., Liebman S. W. The translational function of nucleotide C1054 in the small subunit rRNA is conserved throughout evolution: genetic evidence in yeast. Proc Natl Acad Sci U S A. 1996 Mar 19;93(6):2517–2522. doi: 10.1073/pnas.93.6.2517. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gregory S. T., Dahlberg A. E. Nonsense suppressor and antisuppressor mutations at the 1409-1491 base pair in the decoding region of Escherichia coli 16S rRNA. Nucleic Acids Res. 1995 Nov 11;23(21):4234–4238. doi: 10.1093/nar/23.21.4234. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hausner T. P., Atmadja J., Nierhaus K. H. Evidence that the G2661 region of 23S rRNA is located at the ribosomal binding sites of both elongation factors. Biochimie. 1987 Sep;69(9):911–923. doi: 10.1016/0300-9084(87)90225-2. [DOI] [PubMed] [Google Scholar]
- Holmberg L., Nygård O. Interaction sites of ribosome-bound eukaryotic elongation factor 2 in 18S and 28S rRNA. Biochemistry. 1994 Dec 20;33(50):15159–15167. doi: 10.1021/bi00254a027. [DOI] [PubMed] [Google Scholar]
- Hughes D., Atkins J. F., Thompson S. Mutants of elongation factor Tu promote ribosomal frameshifting and nonsense readthrough. EMBO J. 1987 Dec 20;6(13):4235–4239. doi: 10.1002/j.1460-2075.1987.tb02772.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kunkel T. A., Bebenek K., McClary J. Efficient site-directed mutagenesis using uracil-containing DNA. Methods Enzymol. 1991;204:125–139. doi: 10.1016/0076-6879(91)04008-c. [DOI] [PubMed] [Google Scholar]
- Liu R., Liebman S. W. A translational fidelity mutation in the universally conserved sarcin/ricin domain of 25S yeast ribosomal RNA. RNA. 1996 Mar;2(3):254–263. [PMC free article] [PubMed] [Google Scholar]
- Marchant A., Hartley M. R. Mutational studies on the alpha-sarcin loop of Escherichia coli 23S ribosomal RNA. Eur J Biochem. 1994 Nov 15;226(1):141–147. doi: 10.1111/j.1432-1033.1994.tb20035.x. [DOI] [PubMed] [Google Scholar]
- Melançon P., Tapprich W. E., Brakier-Gingras L. Single-base mutations at position 2661 of Escherichia coli 23S rRNA increase efficiency of translational proofreading. J Bacteriol. 1992 Dec;174(24):7896–7901. doi: 10.1128/jb.174.24.7896-7901.1992. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Moazed D., Robertson J. M., Noller H. F. Interaction of elongation factors EF-G and EF-Tu with a conserved loop in 23S RNA. Nature. 1988 Jul 28;334(6180):362–364. doi: 10.1038/334362a0. [DOI] [PubMed] [Google Scholar]
- O'Connor M., Dahlberg A. E. Mutations at U2555, a tRNA-protected base in 23S rRNA, affect translational fidelity. Proc Natl Acad Sci U S A. 1993 Oct 1;90(19):9214–9218. doi: 10.1073/pnas.90.19.9214. [DOI] [PMC free article] [PubMed] [Google Scholar]
- O'Connor M., Dahlberg A. E. The involvement of two distinct regions of 23 S ribosomal RNA in tRNA selection. J Mol Biol. 1995 Dec 15;254(5):838–847. doi: 10.1006/jmbi.1995.0659. [DOI] [PubMed] [Google Scholar]
- O'Connor M., Göringer H. U., Dahlberg A. E. A ribosomal ambiguity mutation in the 530 loop of E. coli 16S rRNA. Nucleic Acids Res. 1992 Aug 25;20(16):4221–4227. doi: 10.1093/nar/20.16.4221. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Powers T., Noller H. F. Evidence for functional interaction between elongation factor Tu and 16S ribosomal RNA. Proc Natl Acad Sci U S A. 1993 Feb 15;90(4):1364–1368. doi: 10.1073/pnas.90.4.1364. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rodnina M. V., Fricke R., Kuhn L., Wintermeyer W. Codon-dependent conformational change of elongation factor Tu preceding GTP hydrolysis on the ribosome. EMBO J. 1995 Jun 1;14(11):2613–2619. doi: 10.1002/j.1460-2075.1995.tb07259.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Rodnina M. V., Pape T., Fricke R., Kuhn L., Wintermeyer W. Initial binding of the elongation factor Tu.GTP.aminoacyl-tRNA complex preceding codon recognition on the ribosome. J Biol Chem. 1996 Jan 12;271(2):646–652. doi: 10.1074/jbc.271.2.646. [DOI] [PubMed] [Google Scholar]
- Sandbaken M. G., Culbertson M. R. Mutations in elongation factor EF-1 alpha affect the frequency of frameshifting and amino acid misincorporation in Saccharomyces cerevisiae. Genetics. 1988 Dec;120(4):923–934. doi: 10.1093/genetics/120.4.923. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Sigmund C. D., Ettayebi M., Borden A., Morgan E. A. Antibiotic resistance mutations in ribosomal RNA genes of Escherichia coli. Methods Enzymol. 1988;164:673–690. doi: 10.1016/s0076-6879(88)64077-8. [DOI] [PubMed] [Google Scholar]
- Szewczak A. A., Moore P. B., Chang Y. L., Wool I. G. The conformation of the sarcin/ricin loop from 28S ribosomal RNA. Proc Natl Acad Sci U S A. 1993 Oct 15;90(20):9581–9585. doi: 10.1073/pnas.90.20.9581. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Takeshita S., Sato M., Toba M., Masahashi W., Hashimoto-Gotoh T. High-copy-number and low-copy-number plasmid vectors for lacZ alpha-complementation and chloramphenicol- or kanamycin-resistance selection. Gene. 1987;61(1):63–74. doi: 10.1016/0378-1119(87)90365-9. [DOI] [PubMed] [Google Scholar]
- Tapprich W. E., Dahlberg A. E. A single base mutation at position 2661 in E. coli 23S ribosomal RNA affects the binding of ternary complex to the ribosome. EMBO J. 1990 Aug;9(8):2649–2655. doi: 10.1002/j.1460-2075.1990.tb07447.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wool I. G., Glück A., Endo Y. Ribotoxin recognition of ribosomal RNA and a proposal for the mechanism of translocation. Trends Biochem Sci. 1992 Jul;17(7):266–269. doi: 10.1016/0968-0004(92)90407-z. [DOI] [PubMed] [Google Scholar]