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Analysis of translating mitoribosome reveals functional characteristics of translation in mitochondria of fungi
Mitoribosomes are specialized protein synthesis machineries in mitochondria. However, how mRNA binds to its dedicated channel, and tRNA moves as the mitoribosomal subunit rotate with respect to each other is not understood. We report models of the translating fungal mitoribosome with mRNA, tRNA and...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7560712/ https://www.ncbi.nlm.nih.gov/pubmed/33056988 http://dx.doi.org/10.1038/s41467-020-18830-w |
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author | Itoh, Yuzuru Naschberger, Andreas Mortezaei, Narges Herrmann, Johannes M. Amunts, Alexey |
author_facet | Itoh, Yuzuru Naschberger, Andreas Mortezaei, Narges Herrmann, Johannes M. Amunts, Alexey |
author_sort | Itoh, Yuzuru |
collection | PubMed |
description | Mitoribosomes are specialized protein synthesis machineries in mitochondria. However, how mRNA binds to its dedicated channel, and tRNA moves as the mitoribosomal subunit rotate with respect to each other is not understood. We report models of the translating fungal mitoribosome with mRNA, tRNA and nascent polypeptide, as well as an assembly intermediate. Nicotinamide adenine dinucleotide (NAD) is found in the central protuberance of the large subunit, and the ATPase inhibitory factor 1 (IF(1)) in the small subunit. The models of the active mitoribosome explain how mRNA binds through a dedicated protein platform on the small subunit, tRNA is translocated with the help of the protein mL108, bridging it with L1 stalk on the large subunit, and nascent polypeptide paths through a newly shaped exit tunnel involving a series of structural rearrangements. An assembly intermediate is modeled with the maturation factor Atp25, providing insight into the biogenesis of the mitoribosomal large subunit and translation regulation. |
format | Online Article Text |
id | pubmed-7560712 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75607122020-10-19 Analysis of translating mitoribosome reveals functional characteristics of translation in mitochondria of fungi Itoh, Yuzuru Naschberger, Andreas Mortezaei, Narges Herrmann, Johannes M. Amunts, Alexey Nat Commun Article Mitoribosomes are specialized protein synthesis machineries in mitochondria. However, how mRNA binds to its dedicated channel, and tRNA moves as the mitoribosomal subunit rotate with respect to each other is not understood. We report models of the translating fungal mitoribosome with mRNA, tRNA and nascent polypeptide, as well as an assembly intermediate. Nicotinamide adenine dinucleotide (NAD) is found in the central protuberance of the large subunit, and the ATPase inhibitory factor 1 (IF(1)) in the small subunit. The models of the active mitoribosome explain how mRNA binds through a dedicated protein platform on the small subunit, tRNA is translocated with the help of the protein mL108, bridging it with L1 stalk on the large subunit, and nascent polypeptide paths through a newly shaped exit tunnel involving a series of structural rearrangements. An assembly intermediate is modeled with the maturation factor Atp25, providing insight into the biogenesis of the mitoribosomal large subunit and translation regulation. Nature Publishing Group UK 2020-10-14 /pmc/articles/PMC7560712/ /pubmed/33056988 http://dx.doi.org/10.1038/s41467-020-18830-w Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Itoh, Yuzuru Naschberger, Andreas Mortezaei, Narges Herrmann, Johannes M. Amunts, Alexey Analysis of translating mitoribosome reveals functional characteristics of translation in mitochondria of fungi |
title | Analysis of translating mitoribosome reveals functional characteristics of translation in mitochondria of fungi |
title_full | Analysis of translating mitoribosome reveals functional characteristics of translation in mitochondria of fungi |
title_fullStr | Analysis of translating mitoribosome reveals functional characteristics of translation in mitochondria of fungi |
title_full_unstemmed | Analysis of translating mitoribosome reveals functional characteristics of translation in mitochondria of fungi |
title_short | Analysis of translating mitoribosome reveals functional characteristics of translation in mitochondria of fungi |
title_sort | analysis of translating mitoribosome reveals functional characteristics of translation in mitochondria of fungi |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7560712/ https://www.ncbi.nlm.nih.gov/pubmed/33056988 http://dx.doi.org/10.1038/s41467-020-18830-w |
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