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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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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. |
format | Online Article Text |
id | pubmed-6367999 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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