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Structural Patching Fosters Divergence of Mitochondrial Ribosomes

Mitochondrial ribosomes (mitoribosomes) are essential components of all mitochondria that synthesize proteins encoded by the mitochondrial genome. Unlike other ribosomes, mitoribosomes are highly variable across species. The basis for this diversity is not known. Here, we examine the composition and...

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Autores principales: Petrov, Anton S, Wood, Elizabeth C, Bernier, Chad R, Norris, Ashlyn M, Brown, Alan, Amunts, Alexey
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367999/
https://www.ncbi.nlm.nih.gov/pubmed/30517740
http://dx.doi.org/10.1093/molbev/msy221
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author Petrov, Anton S
Wood, Elizabeth C
Bernier, Chad R
Norris, Ashlyn M
Brown, Alan
Amunts, Alexey
author_facet Petrov, Anton S
Wood, Elizabeth C
Bernier, Chad R
Norris, Ashlyn M
Brown, Alan
Amunts, Alexey
author_sort Petrov, Anton S
collection PubMed
description Mitochondrial ribosomes (mitoribosomes) are essential components of all mitochondria that synthesize proteins encoded by the mitochondrial genome. Unlike other ribosomes, mitoribosomes are highly variable across species. The basis for this diversity is not known. Here, we examine the composition and evolutionary history of mitoribosomes across the phylogenetic tree by combining three-dimensional structural information with a comparative analysis of the secondary structures of mitochondrial rRNAs (mt-rRNAs) and available proteomic data. We generate a map of the acquisition of structural variation and reconstruct the fundamental stages that shaped the evolution of the mitoribosomal large subunit and led to this diversity. Our analysis suggests a critical role for ablation and expansion of rapidly evolving mt-rRNA. These changes cause structural instabilities that are “patched” by the acquisition of pre-existing compensatory elements, thus providing opportunities for rapid evolution. This mechanism underlies the incorporation of mt-tRNA into the central protuberance of the mammalian mitoribosome, and the altered path of the polypeptide exit tunnel of the yeast mitoribosome. We propose that since the toolkits of elements utilized for structural patching differ between mitochondria of different species, it fosters the growing divergence of mitoribosomes.
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spelling pubmed-63679992019-02-20 Structural Patching Fosters Divergence of Mitochondrial Ribosomes Petrov, Anton S Wood, Elizabeth C Bernier, Chad R Norris, Ashlyn M Brown, Alan Amunts, Alexey Mol Biol Evol Fast Track Mitochondrial ribosomes (mitoribosomes) are essential components of all mitochondria that synthesize proteins encoded by the mitochondrial genome. Unlike other ribosomes, mitoribosomes are highly variable across species. The basis for this diversity is not known. Here, we examine the composition and evolutionary history of mitoribosomes across the phylogenetic tree by combining three-dimensional structural information with a comparative analysis of the secondary structures of mitochondrial rRNAs (mt-rRNAs) and available proteomic data. We generate a map of the acquisition of structural variation and reconstruct the fundamental stages that shaped the evolution of the mitoribosomal large subunit and led to this diversity. Our analysis suggests a critical role for ablation and expansion of rapidly evolving mt-rRNA. These changes cause structural instabilities that are “patched” by the acquisition of pre-existing compensatory elements, thus providing opportunities for rapid evolution. This mechanism underlies the incorporation of mt-tRNA into the central protuberance of the mammalian mitoribosome, and the altered path of the polypeptide exit tunnel of the yeast mitoribosome. We propose that since the toolkits of elements utilized for structural patching differ between mitochondria of different species, it fosters the growing divergence of mitoribosomes. Oxford University Press 2019-02 2018-12-04 /pmc/articles/PMC6367999/ /pubmed/30517740 http://dx.doi.org/10.1093/molbev/msy221 Text en © The Author(s) 2018. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 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 Fast Track
Petrov, Anton S
Wood, Elizabeth C
Bernier, Chad R
Norris, Ashlyn M
Brown, Alan
Amunts, Alexey
Structural Patching Fosters Divergence of Mitochondrial Ribosomes
title Structural Patching Fosters Divergence of Mitochondrial Ribosomes
title_full Structural Patching Fosters Divergence of Mitochondrial Ribosomes
title_fullStr Structural Patching Fosters Divergence of Mitochondrial Ribosomes
title_full_unstemmed Structural Patching Fosters Divergence of Mitochondrial Ribosomes
title_short Structural Patching Fosters Divergence of Mitochondrial Ribosomes
title_sort structural patching fosters divergence of mitochondrial ribosomes
topic Fast Track
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367999/
https://www.ncbi.nlm.nih.gov/pubmed/30517740
http://dx.doi.org/10.1093/molbev/msy221
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