Structural insights into the translational infidelity mechanism

The decoding of mRNA on the ribosome is the least accurate process during genetic information transfer. Here we propose a unified decoding mechanism based on 11 high-resolution X-ray structures of the 70S ribosome that explains the occurrence of missense errors during translation. We determined ribosome structures in rare states where incorrect tRNAs were incorporated into the peptidyl-tRNA-binding site. These structures show that in the codon–anticodon duplex, a G·U mismatch adopts the Watson–Crick geometry, indicating a shift in the tautomeric equilibrium or ionization of the nucleobase. Additional structures with mismatches in the 70S decoding centre show that the binding of any tRNA induces identical rearrangements in the centre, which favours either isosteric or close to the Watson–Crick geometry codon–anticodon pairs. Overall, the results suggest that a mismatch escapes discrimination by preserving the shape of a Watson–Crick pair and indicate that geometric selection via tautomerism or ionization dominates the translational infidelity mechanism.

[1]  Franck A. P. Vendeix,et al.  Mechanism of expanding the decoding capacity of tRNAs by modification of uridines , 2007, Nature Structural &Molecular Biology.

[2]  M. Rodnina,et al.  Evolutionary optimization of speed and accuracy of decoding on the ribosome , 2011, Philosophical Transactions of the Royal Society B: Biological Sciences.

[3]  R. Morris,et al.  Queuosine modification of tRNA: a case for convergent evolution. , 2001, Molecular genetics and metabolism.

[4]  Paul F Agris,et al.  tRNA's modifications bring order to gene expression. , 2008, Current opinion in microbiology.

[5]  J. Parker,et al.  Errors and alternatives in reading the universal genetic code. , 1989, Microbiological reviews.

[6]  J. H. Matthaei,et al.  Characteristics and composition of RNA coding units. , 1962, Proceedings of the National Academy of Sciences of the United States of America.

[7]  P. Emsley,et al.  Features and development of Coot , 2010, Acta crystallographica. Section D, Biological crystallography.

[8]  Prashant K. Khade,et al.  Steric complementarity in the decoding center is important for tRNA selection by the ribosome. , 2013, Journal of molecular biology.

[9]  B. Shen,et al.  Global mapping of translation initiation sites in mammalian cells at single-nucleotide resolution , 2012, Proceedings of the National Academy of Sciences.

[10]  S. Pestka Studies on the formation of transfer ribonucleic acid-ribosome complexes. VI. Oligopeptide synthesis and translocation on ribosomes in the presence and absence of soluble transfer factors. , 1969, The Journal of biological chemistry.

[11]  V. Ramakrishnan,et al.  How mutations in tRNA distant from the anticodon affect the fidelity of decoding , 2010, Nature Structural &Molecular Biology.

[12]  E. Westhof,et al.  Recognition of Watson-Crick base pairs: constraints and limits due to geometric selection and tautomerism , 2014, F1000prime reports.

[13]  M. Rodnina,et al.  Optimization of speed and accuracy of decoding in translation , 2010, The EMBO journal.

[14]  Claus O. Wilke,et al.  Mistranslation-Induced Protein Misfolding as a Dominant Constraint on Coding-Sequence Evolution , 2008, Cell.

[15]  A. Rich,et al.  Three-dimensional structure of yeast phenylalanine transfer RNA at 3. 0Å resolution , 1974, Nature.

[16]  W. Gilbert,et al.  Pseudouridine profiling reveals regulated mRNA pseudouridylation in yeast and human cells , 2014, Nature.

[17]  J. Åqvist,et al.  Why base tautomerization does not cause errors in mRNA decoding on the ribosome , 2014, Nucleic acids research.

[18]  Jianlin Lei,et al.  Visualization of the hybrid state of tRNA binding promoted by spontaneous ratcheting of the ribosome. , 2008, Molecular cell.

[19]  M. D. Topal,et al.  Base pairing and fidelity in codon–anticodon interaction , 1976, Nature.

[20]  E. Westhof,et al.  New structural insights into the decoding mechanism: Translation infidelity via a G·U pair with Watson–Crick geometry , 2013, FEBS letters.

[21]  Randy J. Read,et al.  Acta Crystallographica Section D Biological , 2003 .

[22]  M. Yusupov,et al.  Structural aspects of messenger RNA reading frame maintenance by the ribosome , 2010, Nature Structural &Molecular Biology.

[23]  J. Collins,et al.  Mistranslation of Membrane Proteins and Two-Component System Activation Trigger Antibiotic-Mediated Cell Death , 2008, Cell.

[24]  E. Westhof,et al.  A new understanding of the decoding principle on the ribosome , 2012, Nature.

[25]  Harry F. Noller,et al.  The Path of Messenger RNA through the Ribosome , 2001, Cell.

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

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

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

[29]  Meitian Wang,et al.  Optimal fine ϕ-slicing for single-photon-counting pixel detectors , 2011, Acta crystallographica. Section D, Biological crystallography.

[30]  M. Selmer,et al.  Structure of the 70S Ribosome Complexed with mRNA and tRNA , 2006, Science.

[31]  T. Kunkel,et al.  Replication infidelity via a mismatch with Watson–Crick geometry , 2011, Proceedings of the National Academy of Sciences.

[32]  P. Farabaugh,et al.  Studies of translational misreading in vivo show that the ribosome very efficiently discriminates against most potential errors , 2014, RNA.

[33]  I. Ial,et al.  Nature Communications , 2010, Nature Cell Biology.

[34]  Michael B. Feldman,et al.  Conformational sampling of aminoacyl-tRNA during selection on the bacterial ribosome. , 2010, Journal of molecular biology.

[35]  H. Al‐Hashimi,et al.  Visualizing transient Watson–Crick-like mispairs in DNA and RNA duplexes , 2015, Nature.

[36]  John Karijolich,et al.  Modifying the genetic code: Converting nonsense codons into sense codons by targeted pseudouridylation , 2011, Nature.

[37]  Ji Wan,et al.  TISdb: a database for alternative translation initiation in mammalian cells , 2013, Nucleic Acids Res..

[38]  R. Thompson,et al.  Proofreading of the codon-anticodon interaction on ribosomes. , 1977, Proceedings of the National Academy of Sciences of the United States of America.

[39]  T. Earnest,et al.  X-ray crystal structures of 70S ribosome functional complexes. , 1999, Science.

[40]  O. Namy,et al.  New insights into the incorporation of natural suppressor tRNAs at stop codons in Saccharomyces cerevisiae , 2014, Nucleic acids research.

[41]  C. Wilke,et al.  The evolutionary consequences of erroneous protein synthesis , 2009, Nature Reviews Genetics.

[42]  A. Spirin,et al.  [43] “Nonenzymatic” translation , 1974 .

[43]  F. Crick,et al.  Genetical Implications of the Structure of Deoxyribonucleic Acid , 1953, Nature.

[44]  H. Hellinga,et al.  Structural evidence for the rare tautomer hypothesis of spontaneous mutagenesis , 2011, Proceedings of the National Academy of Sciences.

[45]  L. P. Gavrilova,et al.  Ribosomal synthesis of polyleucine on polyuridylic acid as a template , 1980, FEBS letters.

[46]  M. Yusupov,et al.  Structural rearrangements of the ribosome at the tRNA proofreading step , 2010, Nature Structural &Molecular Biology.