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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 (m(6)A), 5-methylcytosine (m(5)C) and pseudouridine (Ψ) are highly abundant nucleotide modifications in coding sequences of eukaryal mRNAs, while m(5)C and m(6)A modifications...

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Autores principales: Hoernes, Thomas Philipp, Clementi, Nina, Faserl, Klaus, Glasner, Heidelinde, Breuker, Kathrin, Lindner, Herbert, Hüttenhofer, Alexander, Erlacher, Matthias David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
RNA
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737146/
https://www.ncbi.nlm.nih.gov/pubmed/26578598
http://dx.doi.org/10.1093/nar/gkv1182
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author Hoernes, Thomas Philipp
Clementi, Nina
Faserl, Klaus
Glasner, Heidelinde
Breuker, Kathrin
Lindner, Herbert
Hüttenhofer, Alexander
Erlacher, Matthias David
author_facet Hoernes, Thomas Philipp
Clementi, Nina
Faserl, Klaus
Glasner, Heidelinde
Breuker, Kathrin
Lindner, Herbert
Hüttenhofer, Alexander
Erlacher, Matthias David
author_sort Hoernes, Thomas Philipp
collection PubMed
description Nucleotide modifications within RNA transcripts are found in every organism in all three domains of life. 6-methyladeonsine (m(6)A), 5-methylcytosine (m(5)C) and pseudouridine (Ψ) are highly abundant nucleotide modifications in coding sequences of eukaryal mRNAs, while m(5)C and m(6)A 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 m(5)C, m(6)A, 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 m(5)C 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.
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spelling pubmed-47371462016-02-03 Nucleotide modifications within bacterial messenger RNAs regulate their translation and are able to rewire the genetic code Hoernes, Thomas Philipp Clementi, Nina Faserl, Klaus Glasner, Heidelinde Breuker, Kathrin Lindner, Herbert Hüttenhofer, Alexander Erlacher, Matthias David Nucleic Acids Res RNA Nucleotide modifications within RNA transcripts are found in every organism in all three domains of life. 6-methyladeonsine (m(6)A), 5-methylcytosine (m(5)C) and pseudouridine (Ψ) are highly abundant nucleotide modifications in coding sequences of eukaryal mRNAs, while m(5)C and m(6)A 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 m(5)C, m(6)A, 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 m(5)C 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. Oxford University Press 2016-01-29 2015-11-17 /pmc/articles/PMC4737146/ /pubmed/26578598 http://dx.doi.org/10.1093/nar/gkv1182 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle RNA
Hoernes, Thomas Philipp
Clementi, Nina
Faserl, Klaus
Glasner, Heidelinde
Breuker, Kathrin
Lindner, Herbert
Hüttenhofer, Alexander
Erlacher, Matthias David
Nucleotide modifications within bacterial messenger RNAs regulate their translation and are able to rewire the genetic code
title Nucleotide modifications within bacterial messenger RNAs regulate their translation and are able to rewire the genetic code
title_full Nucleotide modifications within bacterial messenger RNAs regulate their translation and are able to rewire the genetic code
title_fullStr Nucleotide modifications within bacterial messenger RNAs regulate their translation and are able to rewire the genetic code
title_full_unstemmed Nucleotide modifications within bacterial messenger RNAs regulate their translation and are able to rewire the genetic code
title_short Nucleotide modifications within bacterial messenger RNAs regulate their translation and are able to rewire the genetic code
title_sort nucleotide modifications within bacterial messenger rnas regulate their translation and are able to rewire the genetic code
topic RNA
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4737146/
https://www.ncbi.nlm.nih.gov/pubmed/26578598
http://dx.doi.org/10.1093/nar/gkv1182
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