Abstract
We have analyzed by nucleotide analog interference mapping (NAIM) pools of precursor or mature tRNA molecules, carrying a low level of Rp-RMPalphaS (R = A, G, I) or Rp-c7-deaza-RMPalphaS (R = A, G) modifications, to identify functional groups that contribute to the specific interaction with and processing efficiency by Escherichia coli RNase P RNA. The majority of interferences were found in the acceptor stem, T arm, and D arm, including the strongest effects observed at positions G19, G53, A58, and G71. In some cases (interferences at G5, G18, and G71), the affected functional groups are candidates for direct contacts with RNase P RNA. Several modifications disrupt intramolecular tertiary contacts known to stabilize the authentic tRNA fold. Such indirect interference effects were informative as well, because they allowed us to compare the structural constraints required for ptRNA processing versus product binding. Our ptRNA processing and mature tRNA binding NAIM analyses revealed overlapping but nonidentical patterns of interference effects, suggesting that substrate binding and cleavage involves binding modes or conformational states distinct from the binding mode of mature tRNA, the product of the reaction.
Full Text
The Full Text of this article is available as a PDF (1.4 MB).
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Busch S., Kirsebom L. A., Notbohm H., Hartmann R. K. Differential role of the intermolecular base-pairs G292-C(75) and G293-C(74) in the reaction catalyzed by Escherichia coli RNase P RNA. J Mol Biol. 2000 Jun 16;299(4):941–951. doi: 10.1006/jmbi.2000.3789. [DOI] [PubMed] [Google Scholar]
- Chen J. L., Nolan J. M., Harris M. E., Pace N. R. Comparative photocross-linking analysis of the tertiary structures of Escherichia coli and Bacillus subtilis RNase P RNAs. EMBO J. 1998 Mar 2;17(5):1515–1525. doi: 10.1093/emboj/17.5.1515. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chen Y., Li X., Gegenheimer P. Ribonuclease P catalysis requires Mg2+ coordinated to the pro-RP oxygen of the scissile bond. Biochemistry. 1997 Mar 4;36(9):2425–2438. doi: 10.1021/bi9620464. [DOI] [PubMed] [Google Scholar]
- Christian E. L., Yarus M. Analysis of the role of phosphate oxygens in the group I intron from Tetrahymena. J Mol Biol. 1992 Dec 5;228(3):743–758. doi: 10.1016/0022-2836(92)90861-d. [DOI] [PubMed] [Google Scholar]
- Conrad F., Hanne A., Gaur R. K., Krupp G. Enzymatic synthesis of 2'-modified nucleic acids: identification of important phosphate and ribose moieties in RNase P substrates. Nucleic Acids Res. 1995 Jun 11;23(11):1845–1853. doi: 10.1093/nar/23.11.1845. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Frank D. N., Pace N. R. Ribonuclease P: unity and diversity in a tRNA processing ribozyme. Annu Rev Biochem. 1998;67:153–180. doi: 10.1146/annurev.biochem.67.1.153. [DOI] [PubMed] [Google Scholar]
- Gaur R. K., Hanne A., Conrad F., Kahle D., Krupp G. Differences in the interaction of Escherichia coli RNase P RNA with tRNAs containing a short or a long extra arm. RNA. 1996 Jul;2(7):674–681. [PMC free article] [PubMed] [Google Scholar]
- Gaur R. K., Krupp G. Modification interference approach to detect ribose moieties important for the optimal activity of a ribozyme. Nucleic Acids Res. 1993 Jan 11;21(1):21–26. doi: 10.1093/nar/21.1.21. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Guerrier-Takada C., Altman S. A physical assay for and kinetic analysis of the interactions between M1 RNA and tRNA precursor substrates. Biochemistry. 1993 Jul 20;32(28):7152–7161. doi: 10.1021/bi00079a012. [DOI] [PubMed] [Google Scholar]
- Guerrier-Takada C., Gardiner K., Marsh T., Pace N., Altman S. The RNA moiety of ribonuclease P is the catalytic subunit of the enzyme. Cell. 1983 Dec;35(3 Pt 2):849–857. doi: 10.1016/0092-8674(83)90117-4. [DOI] [PubMed] [Google Scholar]
- Hardt W. D., Schlegl J., Erdmann V. A., Hartmann R. K. Gel retardation analysis of E. coli M1 RNA-tRNA complexes. Nucleic Acids Res. 1993 Jul 25;21(15):3521–3527. doi: 10.1093/nar/21.15.3521. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hardt W. D., Schlegl J., Erdmann V. A., Hartmann R. K. Kinetics and thermodynamics of the RNase P RNA cleavage reaction: analysis of tRNA 3'-end variants. J Mol Biol. 1995 Mar 24;247(2):161–172. doi: 10.1006/jmbi.1994.0130. [DOI] [PubMed] [Google Scholar]
- Hardt W. D., Schlegl J., Erdmann V. A., Hartmann R. K. Role of the D arm and the anticodon arm in tRNA recognition by eubacterial and eukaryotic RNase P enzymes. Biochemistry. 1993 Dec 7;32(48):13046–13053. doi: 10.1021/bi00211a014. [DOI] [PubMed] [Google Scholar]
- Hardt W. D., Warnecke J. M., Erdmann V. A., Hartmann R. K. Rp-phosphorothioate modifications in RNase P RNA that interfere with tRNA binding. EMBO J. 1995 Jun 15;14(12):2935–2944. doi: 10.1002/j.1460-2075.1995.tb07293.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Heide C., Pfeiffer T., Nolan J. M., Hartmann R. K. Guanosine 2-NH2 groups of Escherichia coli RNase P RNA involved in intramolecular tertiary contacts and direct interactions with tRNA. RNA. 1999 Jan;5(1):102–116. doi: 10.1017/s1355838299981499. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Holbrook S. R., Sussman J. L., Warrant R. W., Kim S. H. Crystal structure of yeast phenylalanine transfer RNA. II. Structural features and functional implications. J Mol Biol. 1978 Aug 25;123(4):631–660. doi: 10.1016/0022-2836(78)90210-3. [DOI] [PubMed] [Google Scholar]
- Jack A., Ladner J. E., Rhodes D., Brown R. S., Klug A. A crystallographic study of metal-binding to yeast phenylalanine transfer RNA. J Mol Biol. 1977 Apr 15;111(3):315–328. doi: 10.1016/s0022-2836(77)80054-5. [DOI] [PubMed] [Google Scholar]
- Jovine L., Djordjevic S., Rhodes D. The crystal structure of yeast phenylalanine tRNA at 2.0 A resolution: cleavage by Mg(2+) in 15-year old crystals. J Mol Biol. 2000 Aug 11;301(2):401–414. doi: 10.1006/jmbi.2000.3950. [DOI] [PubMed] [Google Scholar]
- Kahle D., Wehmeyer U., Char S., Krupp G. The methylation of one specific guanosine in a pre-tRNA prevents cleavage by RNase P and by the catalytic M1 RNA. Nucleic Acids Res. 1990 Feb 25;18(4):837–844. doi: 10.1093/nar/18.4.837. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kahle D., Wehmeyer U., Krupp G. Substrate recognition by RNase P and by the catalytic M1 RNA: identification of possible contact points in pre-tRNAs. EMBO J. 1990 Jun;9(6):1929–1937. doi: 10.1002/j.1460-2075.1990.tb08320.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kazantsev A. V., Pace N. R. Identification by modification-interference of purine N-7 and ribose 2'-OH groups critical for catalysis by bacterial ribonuclease P. RNA. 1998 Aug;4(8):937–947. doi: 10.1017/s1355838298980384. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kirsebom L. A., Svärd S. G. Base pairing between Escherichia coli RNase P RNA and its substrate. EMBO J. 1994 Oct 17;13(20):4870–4876. doi: 10.1002/j.1460-2075.1994.tb06814.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Kufel J., Kirsebom L. A. Different cleavage sites are aligned differently in the active site of M1 RNA, the catalytic subunit of Escherichia coli RNase P. Proc Natl Acad Sci U S A. 1996 Jun 11;93(12):6085–6090. doi: 10.1073/pnas.93.12.6085. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Loria A., Pan T. Recognition of the T stem-loop of a pre-tRNA substrate by the ribozyme from Bacillus subtilis ribonuclease P. Biochemistry. 1997 May 27;36(21):6317–6325. doi: 10.1021/bi970115o. [DOI] [PubMed] [Google Scholar]
- Massire C., Jaeger L., Westhof E. Derivation of the three-dimensional architecture of bacterial ribonuclease P RNAs from comparative sequence analysis. J Mol Biol. 1998 Jun 19;279(4):773–793. doi: 10.1006/jmbi.1998.1797. [DOI] [PubMed] [Google Scholar]
- Oh B. K., Frank D. N., Pace N. R. Participation of the 3'-CCA of tRNA in the binding of catalytic Mg2+ ions by ribonuclease P. Biochemistry. 1998 May 19;37(20):7277–7283. doi: 10.1021/bi973100z. [DOI] [PubMed] [Google Scholar]
- Oh B. K., Pace N. R. Interaction of the 3'-end of tRNA with ribonuclease P RNA. Nucleic Acids Res. 1994 Oct 11;22(20):4087–4094. doi: 10.1093/nar/22.20.4087. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pan T., Loria A., Zhong K. Probing of tertiary interactions in RNA: 2'-hydroxyl-base contacts between the RNase P RNA and pre-tRNA. Proc Natl Acad Sci U S A. 1995 Dec 19;92(26):12510–12514. doi: 10.1073/pnas.92.26.12510. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pannucci J. A., Haas E. S., Hall T. A., Harris J. K., Brown J. W. RNase P RNAs from some Archaea are catalytically active. Proc Natl Acad Sci U S A. 1999 Jul 6;96(14):7803–7808. doi: 10.1073/pnas.96.14.7803. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Perreault J. P., Altman S. Important 2'-hydroxyl groups in model substrates for M1 RNA, the catalytic RNA subunit of RNase P from Escherichia coli. J Mol Biol. 1992 Jul 20;226(2):399–409. doi: 10.1016/0022-2836(92)90955-j. [DOI] [PubMed] [Google Scholar]
- Pomeranz Krummel D. A., Altman S. Multiple binding modes of substrate to the catalytic RNA subunit of RNase P from Escherichia coli. RNA. 1999 Aug;5(8):1021–1033. doi: 10.1017/s1355838299990416. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Quigley G. J., Rich A. Structural domains of transfer RNA molecules. Science. 1976 Nov 19;194(4267):796–806. doi: 10.1126/science.790568. [DOI] [PubMed] [Google Scholar]
- Rich A., RajBhandary U. L. Transfer RNA: molecular structure, sequence, and properties. Annu Rev Biochem. 1976;45:805–860. doi: 10.1146/annurev.bi.45.070176.004105. [DOI] [PubMed] [Google Scholar]
- Smith D., Pace N. R. Multiple magnesium ions in the ribonuclease P reaction mechanism. Biochemistry. 1993 May 25;32(20):5273–5281. doi: 10.1021/bi00071a001. [DOI] [PubMed] [Google Scholar]
- Warnecke J. M., Fürste J. P., Hardt W. D., Erdmann V. A., Hartmann R. K. Ribonuclease P (RNase P) RNA is converted to a Cd(2+)-ribozyme by a single Rp-phosphorothioate modification in the precursor tRNA at the RNase P cleavage site. Proc Natl Acad Sci U S A. 1996 Aug 20;93(17):8924–8928. doi: 10.1073/pnas.93.17.8924. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Westhof E., Dumas P., Moras D. Crystallographic refinement of yeast aspartic acid transfer RNA. J Mol Biol. 1985 Jul 5;184(1):119–145. doi: 10.1016/0022-2836(85)90048-8. [DOI] [PubMed] [Google Scholar]
- Westhof E., Sundaralingam M. Restrained refinement of the monoclinic form of yeast phenylalanine transfer RNA. Temperature factors and dynamics, coordinated waters, and base-pair propeller twist angles. Biochemistry. 1986 Aug 26;25(17):4868–4878. doi: 10.1021/bi00365a022. [DOI] [PubMed] [Google Scholar]
- Westhof E., Wesolowski D., Altman S. Mapping in three dimensions of regions in a catalytic RNA protected from attack by an Fe(II)-EDTA reagent. J Mol Biol. 1996 May 17;258(4):600–613. doi: 10.1006/jmbi.1996.0272. [DOI] [PubMed] [Google Scholar]