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Eukaryotic life without tQ(CUG): the role of Elongator-dependent tRNA modifications in Dictyostelium discoideum

In the Elongator-dependent modification pathway, chemical modifications are introduced at the wobble uridines at position 34 in transfer RNAs (tRNAs), which serve to optimize codon translation rates. Here, we show that this three-step modification pathway exists in Dictyostelium discoideum, model of...

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Autores principales: Schäck, Manfred A, Jablonski, Kim Philipp, Gräf, Stefan, Klassen, Roland, Schaffrath, Raffael, Kellner, Stefanie, Hammann, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430636/
https://www.ncbi.nlm.nih.gov/pubmed/32609816
http://dx.doi.org/10.1093/nar/gkaa560
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author Schäck, Manfred A
Jablonski, Kim Philipp
Gräf, Stefan
Klassen, Roland
Schaffrath, Raffael
Kellner, Stefanie
Hammann, Christian
author_facet Schäck, Manfred A
Jablonski, Kim Philipp
Gräf, Stefan
Klassen, Roland
Schaffrath, Raffael
Kellner, Stefanie
Hammann, Christian
author_sort Schäck, Manfred A
collection PubMed
description In the Elongator-dependent modification pathway, chemical modifications are introduced at the wobble uridines at position 34 in transfer RNAs (tRNAs), which serve to optimize codon translation rates. Here, we show that this three-step modification pathway exists in Dictyostelium discoideum, model of the evolutionary superfamily Amoebozoa. Not only are previously established modifications observable by mass spectrometry in strains with the most conserved genes of each step deleted, but also additional modifications are detected, indicating a certain plasticity of the pathway in the amoeba. Unlike described for yeast, D. discoideum allows for an unconditional deletion of the single tQ(CUG) gene, as long as the Elongator-dependent modification pathway is intact. In gene deletion strains of the modification pathway, protein amounts are significantly reduced as shown by flow cytometry and Western blotting, using strains expressing different glutamine leader constructs fused to GFP. Most dramatic are these effects, when the tQ(CUG) gene is deleted, or Elp3, the catalytic component of the Elongator complex is missing. In addition, Elp3 is the most strongly conserved protein of the modification pathway, as our phylogenetic analysis reveals. The implications of this observation are discussed with respect to the evolutionary age of the components acting in the Elongator-dependent modification pathway.
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spelling pubmed-74306362020-08-19 Eukaryotic life without tQ(CUG): the role of Elongator-dependent tRNA modifications in Dictyostelium discoideum Schäck, Manfred A Jablonski, Kim Philipp Gräf, Stefan Klassen, Roland Schaffrath, Raffael Kellner, Stefanie Hammann, Christian Nucleic Acids Res Molecular Biology In the Elongator-dependent modification pathway, chemical modifications are introduced at the wobble uridines at position 34 in transfer RNAs (tRNAs), which serve to optimize codon translation rates. Here, we show that this three-step modification pathway exists in Dictyostelium discoideum, model of the evolutionary superfamily Amoebozoa. Not only are previously established modifications observable by mass spectrometry in strains with the most conserved genes of each step deleted, but also additional modifications are detected, indicating a certain plasticity of the pathway in the amoeba. Unlike described for yeast, D. discoideum allows for an unconditional deletion of the single tQ(CUG) gene, as long as the Elongator-dependent modification pathway is intact. In gene deletion strains of the modification pathway, protein amounts are significantly reduced as shown by flow cytometry and Western blotting, using strains expressing different glutamine leader constructs fused to GFP. Most dramatic are these effects, when the tQ(CUG) gene is deleted, or Elp3, the catalytic component of the Elongator complex is missing. In addition, Elp3 is the most strongly conserved protein of the modification pathway, as our phylogenetic analysis reveals. The implications of this observation are discussed with respect to the evolutionary age of the components acting in the Elongator-dependent modification pathway. Oxford University Press 2020-07-01 /pmc/articles/PMC7430636/ /pubmed/32609816 http://dx.doi.org/10.1093/nar/gkaa560 Text en © The Author(s) 2020. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Molecular Biology
Schäck, Manfred A
Jablonski, Kim Philipp
Gräf, Stefan
Klassen, Roland
Schaffrath, Raffael
Kellner, Stefanie
Hammann, Christian
Eukaryotic life without tQ(CUG): the role of Elongator-dependent tRNA modifications in Dictyostelium discoideum
title Eukaryotic life without tQ(CUG): the role of Elongator-dependent tRNA modifications in Dictyostelium discoideum
title_full Eukaryotic life without tQ(CUG): the role of Elongator-dependent tRNA modifications in Dictyostelium discoideum
title_fullStr Eukaryotic life without tQ(CUG): the role of Elongator-dependent tRNA modifications in Dictyostelium discoideum
title_full_unstemmed Eukaryotic life without tQ(CUG): the role of Elongator-dependent tRNA modifications in Dictyostelium discoideum
title_short Eukaryotic life without tQ(CUG): the role of Elongator-dependent tRNA modifications in Dictyostelium discoideum
title_sort eukaryotic life without tq(cug): the role of elongator-dependent trna modifications in dictyostelium discoideum
topic Molecular Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7430636/
https://www.ncbi.nlm.nih.gov/pubmed/32609816
http://dx.doi.org/10.1093/nar/gkaa560
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