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Small but large enough: structural properties of armless mitochondrial tRNAs from the nematode Romanomermis culicivorax

As adapter molecules to convert the nucleic acid information into the amino acid sequence, tRNAs play a central role in protein synthesis. To fulfill this function in a reliable way, tRNAs exhibit highly conserved structural features common in all organisms and in all cellular compartments active in...

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Autores principales: Jühling, Tina, Duchardt-Ferner, Elke, Bonin, Sonja, Wöhnert, Jens, Pütz, Joern, Florentz, Catherine, Betat, Heike, Sauter, Claude, Mörl, Mario
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6158502/
https://www.ncbi.nlm.nih.gov/pubmed/29986062
http://dx.doi.org/10.1093/nar/gky593
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author Jühling, Tina
Duchardt-Ferner, Elke
Bonin, Sonja
Wöhnert, Jens
Pütz, Joern
Florentz, Catherine
Betat, Heike
Sauter, Claude
Mörl, Mario
author_facet Jühling, Tina
Duchardt-Ferner, Elke
Bonin, Sonja
Wöhnert, Jens
Pütz, Joern
Florentz, Catherine
Betat, Heike
Sauter, Claude
Mörl, Mario
author_sort Jühling, Tina
collection PubMed
description As adapter molecules to convert the nucleic acid information into the amino acid sequence, tRNAs play a central role in protein synthesis. To fulfill this function in a reliable way, tRNAs exhibit highly conserved structural features common in all organisms and in all cellular compartments active in translation. However, in mitochondria of metazoans, certain dramatic deviations from the consensus tRNA structure are described, where some tRNAs lack the D- or T-arm without losing their function. In Enoplea, this miniaturization comes to an extreme, and functional mitochondrial tRNAs can lack both arms, leading to a considerable size reduction. Here, we investigate the secondary and tertiary structure of two such armless tRNAs from Romanomermis culicivorax. Despite their high AU content, the transcripts fold into a single and surprisingly stable hairpin structure, deviating from standard tRNAs. The three-dimensional form is boomerang-like and diverges from the standard L-shape. These results indicate that such unconventional miniaturized tRNAs can still fold into a tRNA-like shape, although their length and secondary structure are very unusual. They highlight the remarkable flexibility of the protein synthesis apparatus and suggest that the translational machinery of Enoplea mitochondria may show compensatory adaptations to accommodate these armless tRNAs for efficient translation.
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spelling pubmed-61585022018-10-02 Small but large enough: structural properties of armless mitochondrial tRNAs from the nematode Romanomermis culicivorax Jühling, Tina Duchardt-Ferner, Elke Bonin, Sonja Wöhnert, Jens Pütz, Joern Florentz, Catherine Betat, Heike Sauter, Claude Mörl, Mario Nucleic Acids Res RNA and RNA-protein complexes As adapter molecules to convert the nucleic acid information into the amino acid sequence, tRNAs play a central role in protein synthesis. To fulfill this function in a reliable way, tRNAs exhibit highly conserved structural features common in all organisms and in all cellular compartments active in translation. However, in mitochondria of metazoans, certain dramatic deviations from the consensus tRNA structure are described, where some tRNAs lack the D- or T-arm without losing their function. In Enoplea, this miniaturization comes to an extreme, and functional mitochondrial tRNAs can lack both arms, leading to a considerable size reduction. Here, we investigate the secondary and tertiary structure of two such armless tRNAs from Romanomermis culicivorax. Despite their high AU content, the transcripts fold into a single and surprisingly stable hairpin structure, deviating from standard tRNAs. The three-dimensional form is boomerang-like and diverges from the standard L-shape. These results indicate that such unconventional miniaturized tRNAs can still fold into a tRNA-like shape, although their length and secondary structure are very unusual. They highlight the remarkable flexibility of the protein synthesis apparatus and suggest that the translational machinery of Enoplea mitochondria may show compensatory adaptations to accommodate these armless tRNAs for efficient translation. Oxford University Press 2018-09-28 2018-07-09 /pmc/articles/PMC6158502/ /pubmed/29986062 http://dx.doi.org/10.1093/nar/gky593 Text en © The Author(s) 2018. 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 RNA and RNA-protein complexes
Jühling, Tina
Duchardt-Ferner, Elke
Bonin, Sonja
Wöhnert, Jens
Pütz, Joern
Florentz, Catherine
Betat, Heike
Sauter, Claude
Mörl, Mario
Small but large enough: structural properties of armless mitochondrial tRNAs from the nematode Romanomermis culicivorax
title Small but large enough: structural properties of armless mitochondrial tRNAs from the nematode Romanomermis culicivorax
title_full Small but large enough: structural properties of armless mitochondrial tRNAs from the nematode Romanomermis culicivorax
title_fullStr Small but large enough: structural properties of armless mitochondrial tRNAs from the nematode Romanomermis culicivorax
title_full_unstemmed Small but large enough: structural properties of armless mitochondrial tRNAs from the nematode Romanomermis culicivorax
title_short Small but large enough: structural properties of armless mitochondrial tRNAs from the nematode Romanomermis culicivorax
title_sort small but large enough: structural properties of armless mitochondrial trnas from the nematode romanomermis culicivorax
topic RNA and RNA-protein complexes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6158502/
https://www.ncbi.nlm.nih.gov/pubmed/29986062
http://dx.doi.org/10.1093/nar/gky593
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