Nucleotide modifications within bacterial messenger RNAs regulate their translation and are able to rewire the genetic code

Nucleotide modifications within RNA transcripts are found in every organism in all three domains of life. 6-methyladeonsine (m6A), 5-methylcytosine (m5C) and pseudouridine (Ψ) are highly abundant nucleotide modifications in coding sequences of eukaryal mRNAs, while m5C and m6A modifications have also been discovered in archaeal and bacterial mRNAs. Employing in vitro translation assays, we systematically investigated the influence of nucleotide modifications on translation. We introduced m5C, m6A, Ψ or 2′-O-methylated nucleotides at each of the three positions within a codon of the bacterial ErmCL mRNA and analyzed their influence on translation. Depending on the respective nucleotide modification, as well as its position within a codon, protein synthesis remained either unaffected or was prematurely terminated at the modification site, resulting in reduced amounts of the full-length peptide. In the latter case, toeprint analysis of ribosomal complexes was consistent with stalling of translation at the modified codon. When multiple nucleotide modifications were introduced within one codon, an additive inhibitory effect on translation was observed. We also identified the m5C modification to alter the amino acid identity of the corresponding codon, when positioned at the second codon position. Our results suggest a novel mode of gene regulation by nucleotide modifications in bacterial mRNAs.

[1]  J. Hillebrecht,et al.  A comparative study of protein synthesis in in vitro systems: from the prokaryotic reconstituted to the eukaryotic extract-based , 2008, BMC biotechnology.

[2]  V. Ramakrishnan,et al.  Unusual base pairing during the decoding of a stop codon by the ribosome , 2013, Nature.

[3]  Yang Wang,et al.  N6-methyladenosine modification destabilizes developmental regulators in embryonic stem cells , 2014, Nature Cell Biology.

[4]  D. Davis Stabilization of RNA stacking by pseudouridine. , 1995, Nucleic acids research.

[5]  Edouard Bertrand,et al.  ADAR2-mediated editing of RNA substrates in the nucleolus is inhibited by C/D small nucleolar RNAs , 2005, The Journal of cell biology.

[6]  J. Rosenecker,et al.  Expression of therapeutic proteins after delivery of chemically modified mRNA in mice , 2011, Nature Biotechnology.

[7]  A. Mankin,et al.  Molecular mechanism of drug-dependent ribosome stalling. , 2008, Molecular cell.

[8]  Henri Grosjean,et al.  Fine-tuning of RNA functions by modification and editing , 2005 .

[9]  A. Hüttenhofer,et al.  RNomics: an experimental approach that identifies 201 candidates for novel, small, non‐messenger RNAs in mouse , 2001, The EMBO journal.

[10]  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.

[11]  Schraga Schwartz,et al.  Transcriptome-Wide Mapping of 5-methylcytidine RNA Modifications in Bacteria, Archaea, and Yeast Reveals m5C within Archaeal mRNAs , 2013, PLoS genetics.

[12]  A. Chirkova,et al.  Generation of chemically engineered ribosomes for atomic mutagenesis studies on protein biosynthesis , 2011, Nature Protocols.

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

[14]  T. Preiss,et al.  Widespread occurrence of 5-methylcytosine in human coding and non-coding RNA , 2012, Nucleic acids research.

[15]  Maxwell R. Mumbach,et al.  Transcriptome-wide Mapping Reveals Widespread Dynamic-Regulated Pseudouridylation of ncRNA and mRNA , 2014, Cell.

[16]  Lydia M. Contreras,et al.  Functional implications of ribosomal RNA methylation in response to environmental stress , 2014, Critical reviews in biochemistry and molecular biology.

[17]  Hani S. Zaher,et al.  O6-Methylguanosine leads to position-dependent effects on ribosome speed and fidelity , 2015, RNA.

[18]  A. Hüttenhofer,et al.  The expanding snoRNA world. , 2002, Biochimie.

[19]  V. Narry Kim,et al.  Emerging Roles of RNA Modification: m6A and U-Tail , 2014, Cell.

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

[21]  S. Stamm,et al.  The snoRNA HBII-52 Regulates Alternative Splicing of the Serotonin Receptor 2C , 2006, Science.

[22]  Chuan He,et al.  Pseudouridine in a new era of RNA modifications , 2014, Cell Research.

[23]  Samie R. Jaffrey,et al.  The dynamic epitranscriptome: N6-methyladenosine and gene expression control , 2014, Nature Reviews Molecular Cell Biology.

[24]  T. Pan N6-methyl-adenosine modification in messenger and long non-coding RNA. , 2013, Trends in biochemical sciences.

[25]  R. Micura,et al.  The preparation of site-specifically modified riboswitch domains as an example for enzymatic ligation of chemically synthesized RNA fragments , 2008, Nature Protocols.

[26]  Thomas Preiss,et al.  Mapping and significance of the mRNA methylome , 2013, Wiley interdisciplinary reviews. RNA.

[27]  J. Bujnicki,et al.  MODOMICS: a database of RNA modification pathways—2013 update , 2012, Nucleic Acids Res..

[28]  Gideon Rechavi,et al.  Gene expression regulation mediated through reversible m6A RNA methylation , 2014, Nature Reviews Genetics.

[29]  M. Yusupov,et al.  High-resolution structure of the eukaryotic 80S ribosome. , 2014, Annual review of biochemistry.

[30]  Chuan He,et al.  N 6 -methyladenosine Modulates Messenger RNA Translation Efficiency , 2015, Cell.

[31]  M. Tuck,et al.  Internal 6-methyladenine residues increase the in vitro translation efficiency of dihydrofolate reductase messenger RNA. , 1996, The international journal of biochemistry & cell biology.

[32]  Sebastian A. Leidel,et al.  Modify or die? - RNA modification defects in metazoans , 2014, RNA biology.

[33]  P. Sergiev,et al.  What do we know about ribosomal RNA methylation in Escherichia coli? , 2015, Biochimie.

[34]  V. de Crécy-Lagard,et al.  Biosynthesis and function of posttranscriptional modifications of transfer RNAs. , 2012, Annual review of genetics.

[35]  H. Schägger Tricine–SDS-PAGE , 2006, Nature Protocols.

[36]  B. Moss,et al.  Methylated nucleotides block 5′ terminus of HeLa cell messenger RNA , 1975, Cell.

[37]  U. Bommer Ribosomes and polysomes , 1997 .

[38]  T. Steitz,et al.  Structural insights into the role of rRNA modifications in protein synthesis and ribosome assembly , 2015, Nature Structural &Molecular Biology.

[39]  D. Weissman,et al.  Generating the optimal mRNA for therapy: HPLC purification eliminates immune activation and improves translation of nucleoside-modified, protein-encoding mRNA , 2011, Nucleic acids research.

[40]  Hani S. Zaher,et al.  An active role for the ribosome in determining the fate of oxidized mRNA. , 2014, Cell reports.

[41]  Eduard Batlle,et al.  Role of tRNA modifications in human diseases. , 2014, Trends in molecular medicine.

[42]  Shiqing Ma,et al.  Chemical pulldown reveals dynamic pseudouridylation of the mammalian transcriptome. , 2015, Nature chemical biology.

[43]  P. Brown,et al.  Transcriptome-Wide Mapping of Pseudouridines: Pseudouridine Synthases Modify Specific mRNAs in S. cerevisiae , 2014, PloS one.

[44]  D. Weissman,et al.  Increased Erythropoiesis in Mice Injected With Submicrogram Quantities of Pseudouridine-containing mRNA Encoding Erythropoietin , 2012, Molecular therapy : the journal of the American Society of Gene Therapy.

[45]  R. Micura,et al.  An intact ribose moiety at A2602 of 23S rRNA is key to trigger peptidyl-tRNA hydrolysis during translation termination , 2007, Nucleic acids research.

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

[47]  Chengqi Yi,et al.  N6-Methyladenosine in Nuclear RNA is a Major Substrate of the Obesity-Associated FTO , 2011, Nature chemical biology.

[48]  Takuya Ueda,et al.  Cell-free translation reconstituted with purified components , 2001, Nature Biotechnology.

[49]  M. Fournier,et al.  Ribosome structure and activity are altered in cells lacking snoRNPs that form pseudouridines in the peptidyl transferase center. , 2003, Molecular cell.

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

[51]  Xin Deng,et al.  Widespread occurrence of N6-methyladenosine in bacterial mRNA , 2015, Nucleic acids research.

[52]  Albert Kriegner,et al.  Methylation of ribosomal RNA by NSUN5 is a conserved mechanism modulating organismal lifespan , 2015, Nature Communications.

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

[54]  T. Pan,et al.  Rationalization and prediction of selective decoding of pseudouridine-modified nonsense and sense codons. , 2012, RNA.

[55]  O. Elemento,et al.  Comprehensive Analysis of mRNA Methylation Reveals Enrichment in 3′ UTRs and near Stop Codons , 2012, Cell.

[56]  Hiroki Kato,et al.  Incorporation of pseudouridine into mRNA yields superior nonimmunogenic vector with increased translational capacity and biological stability. , 2008, Molecular therapy : the journal of the American Society of Gene Therapy.