Mutational analysis reveals two independent molecular requirements during transfer RNA selection on the ribosome

Accurate discrimination between cognate and near-cognate aminoacyl-tRNAs during translation relies on the specific acceleration of forward rate constants for cognate tRNAs. Such specific rate enhancement correlates with conformational changes in the tRNA and small ribosomal subunit that depend on an RNA-specific type of interaction, the A-minor motif, between universally conserved 16S ribosomal RNA nucleotides and the cognate codon-anticodon helix. We show that perturbations of these two components of the A-minor motif, the conserved rRNA bases and the codon-anticodon helix, result in distinct outcomes. Although both cause decreases in the rates of tRNA selection that are rescued by aminoglycoside antibiotics, only disruption of the codon-anticodon helix is overcome by a miscoding tRNA variant. On this basis, we propose that two independent molecular requirements must be met to allow tRNAs to proceed through the selection pathway, providing a mechanism for exquisite control of fidelity during this step in gene expression.

[1]  T. Pape,et al.  Induced fit in initial selection and proofreading of aminoacyl‐tRNA on the ribosome , 1999, The EMBO journal.

[2]  Quantitative analysis of deoxynucleotide substitutions in the codon-anticodon helix. , 2006, Journal of molecular biology.

[3]  R. Buckingham,et al.  tRNA tertiary structure in solution as probed by the photochemically induced 8-13 cross-link. , 1975, Nucleic acids research.

[4]  V. Ramakrishnan,et al.  Recognition of Cognate Transfer RNA by the 30S Ribosomal Subunit , 2001, Science.

[5]  M. Rodnina,et al.  Streptomycin interferes with conformational coupling between codon recognition and GTPase activation on the ribosome , 2004, Nature Structural &Molecular Biology.

[6]  Rachel Green,et al.  The Active Site of the Ribosome Is Composed of Two Layers of Conserved Nucleotides with Distinct Roles in Peptide Bond Formation and Peptide Release , 2004, Cell.

[7]  M. Rodnina,et al.  Kinetic determinants of high-fidelity tRNA discrimination on the ribosome. , 2004, Molecular cell.

[8]  D. Hirsh Tryptophan transfer RNA as the UGA suppressor. , 1971, Journal of molecular biology.

[9]  E. Youngman,et al.  Affinity purification of in vivo-assembled ribosomes for in vitro biochemical analysis. , 2005, Methods.

[10]  H. Noller,et al.  Dominant lethal mutations in a conserved loop in 16S rRNA. , 1990, Proceedings of the National Academy of Sciences of the United States of America.

[11]  M. O'Connor,et al.  Mutations in the Intersubunit Bridge Regions of 23 S rRNA* , 2006, Journal of Biological Chemistry.

[12]  Scott M Stagg,et al.  Incorporation of aminoacyl-tRNA into the ribosome as seen by cryo-electron microscopy , 2003, Nature Structural Biology.

[13]  Tina Daviter,et al.  A uniform response to mismatches in codon-anticodon complexes ensures ribosomal fidelity. , 2006, Molecular cell.

[14]  Jennifer A. Doudna,et al.  A universal mode of helix packing in RNA , 2001, Nature Structural Biology.

[15]  K. Nierhaus,et al.  Ribosomal Decoding Processes at Codons in the A or P Sites Depend Differently on 2′-OH Groups (*) , 1995, The Journal of Biological Chemistry.

[16]  R. Gourse,et al.  Feedback regulation of rRNA and tRNA synthesis and accumulation of free ribosomes after conditional expression of rRNA genes. , 1985, Proceedings of the National Academy of Sciences of the United States of America.

[17]  J L Sussman,et al.  Crystal structure of yeast phenylalanine transfer RNA. II. Structural features and functional implications. , 1978, Journal of molecular biology.

[18]  J. Puglisi,et al.  RNA sequence determinants for aminoglycoside binding to an A-site rRNA model oligonucleotide. , 1996, Journal of molecular biology.

[19]  J. Doudna,et al.  Specificity of RNA–RNA helix recognition , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[20]  O. Uhlenbeck,et al.  Intact aminoacyl-tRNA is required to trigger GTP hydrolysis by elongation factor Tu on the ribosome. , 2000, Biochemistry.

[21]  J. Vacher,et al.  Effect of photochemical crosslink S4U(8)-C(13) on suppressor activity of su+ tRNATrp from Escherichia coli. , 1979, Journal of molecular biology.

[22]  J L Sussman,et al.  Crystal structure of yeast phenylalanine transfer RNA. I. Crystallographic refinement. , 1978, Journal of molecular biology.

[23]  T. Pape,et al.  Conformational switch in the decoding region of 16S rRNA during aminoacyl-tRNA selection on the ribosome , 2000, Nature Structural Biology.

[24]  J. Puglisi,et al.  Recognition of the codon-anticodon helix by ribosomal RNA. , 1999, Science.

[25]  J. Puglisi,et al.  tRNA selection and kinetic proofreading in translation , 2004, Nature Structural &Molecular Biology.

[26]  J. Ninio Kinetic amplification of enzyme discrimination. , 1975, Biochimie.

[27]  V. Ramakrishnan,et al.  First published online as a Review in Advance on February 25, 2005 STRUCTURAL INSIGHTS INTO TRANSLATIONAL , 2022 .

[28]  V. Ramakrishnan,et al.  Functional insights from the structure of the 30S ribosomal subunit and its interactions with antibiotics , 2000, Nature.

[29]  V. Ramakrishnan,et al.  Selection of tRNA by the Ribosome Requires a Transition from an Open to a Closed Form , 2002, Cell.

[30]  Harry F Noller,et al.  RNA Structure: Reading the Ribosome , 2005, Science.

[31]  T. Earnest,et al.  Crystal Structure of the Ribosome at 5.5 Å Resolution , 2001, Science.

[32]  M. Rodnina,et al.  Fidelity of aminoacyl-tRNA selection on the ribosome: kinetic and structural mechanisms. , 2001, Annual review of biochemistry.

[33]  R. Green,et al.  Multiple effects of S13 in modulating the strength of intersubunit interactions in the ribosome during translation. , 2005, Journal of molecular biology.

[34]  Kurt Fredrick,et al.  Contribution of 16S rRNA nucleotides forming the 30S subunit A and P sites to translation in Escherichia coli. , 2005, RNA.

[35]  S. Joseph,et al.  Universally conserved interactions between the ribosome and the anticodon stem-loop of A site tRNA important for translocation. , 2002, Molecular cell.

[36]  T. Pape,et al.  Complete kinetic mechanism of elongation factor Tu‐dependent binding of aminoacyl‐tRNA to the A site of the E.coli ribosome , 1998, The EMBO journal.

[37]  J. Hopfield Kinetic proofreading: a new mechanism for reducing errors in biosynthetic processes requiring high specificity. , 1974, Proceedings of the National Academy of Sciences of the United States of America.

[38]  R. Green,et al.  An Active Role for tRNA in Decoding Beyond Codon:Anticodon Pairing , 2005, Science.

[39]  T. Pape,et al.  Initial Binding of the Elongation Factor Tu·GTP·Aminoacyl-tRNA Complex Preceding Codon Recognition on the Ribosome (*) , 1996, The Journal of Biological Chemistry.