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The human Obg protein GTPBP10 is involved in mitoribosomal biogenesis
The human mitochondrial translation apparatus, which synthesizes the core subunits of the oxidative phosphorylation system, is of central interest as mutations in several genes encoding for mitoribosomal proteins or translation factors cause severe human diseases. Little is known, how this complex m...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144781/ https://www.ncbi.nlm.nih.gov/pubmed/30085210 http://dx.doi.org/10.1093/nar/gky701 |
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author | Lavdovskaia, Elena Kolander, Elisa Steube, Emely Mai, Mandy Mong-Quyen Urlaub, Henning Richter-Dennerlein, Ricarda |
author_facet | Lavdovskaia, Elena Kolander, Elisa Steube, Emely Mai, Mandy Mong-Quyen Urlaub, Henning Richter-Dennerlein, Ricarda |
author_sort | Lavdovskaia, Elena |
collection | PubMed |
description | The human mitochondrial translation apparatus, which synthesizes the core subunits of the oxidative phosphorylation system, is of central interest as mutations in several genes encoding for mitoribosomal proteins or translation factors cause severe human diseases. Little is known, how this complex machinery assembles from nuclear-encoded protein components and mitochondrial-encoded RNAs, and which ancillary factors are required to form a functional mitoribosome. We have characterized the human Obg protein GTPBP10, which associates specifically with the mitoribosomal large subunit at a late maturation state. Defining its interactome, we have shown that GTPBP10 is in a complex with other mtLSU biogenesis factors including mitochondrial RNA granule components, the 16S rRNA module and late mtLSU assembly factors such as MALSU1, SMCR7L, MTERF4 and NSUN4. GTPBP10 deficiency leads to a drastic reduction in 55S monosome formation resulting in defective mtDNA-expression and in a decrease in cell growth. Our results suggest that GTPBP10 is a ribosome biogenesis factor of the mtLSU required for late stages of maturation. |
format | Online Article Text |
id | pubmed-6144781 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-61447812018-09-25 The human Obg protein GTPBP10 is involved in mitoribosomal biogenesis Lavdovskaia, Elena Kolander, Elisa Steube, Emely Mai, Mandy Mong-Quyen Urlaub, Henning Richter-Dennerlein, Ricarda Nucleic Acids Res Molecular Biology The human mitochondrial translation apparatus, which synthesizes the core subunits of the oxidative phosphorylation system, is of central interest as mutations in several genes encoding for mitoribosomal proteins or translation factors cause severe human diseases. Little is known, how this complex machinery assembles from nuclear-encoded protein components and mitochondrial-encoded RNAs, and which ancillary factors are required to form a functional mitoribosome. We have characterized the human Obg protein GTPBP10, which associates specifically with the mitoribosomal large subunit at a late maturation state. Defining its interactome, we have shown that GTPBP10 is in a complex with other mtLSU biogenesis factors including mitochondrial RNA granule components, the 16S rRNA module and late mtLSU assembly factors such as MALSU1, SMCR7L, MTERF4 and NSUN4. GTPBP10 deficiency leads to a drastic reduction in 55S monosome formation resulting in defective mtDNA-expression and in a decrease in cell growth. Our results suggest that GTPBP10 is a ribosome biogenesis factor of the mtLSU required for late stages of maturation. Oxford University Press 2018-09-19 2018-08-02 /pmc/articles/PMC6144781/ /pubmed/30085210 http://dx.doi.org/10.1093/nar/gky701 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 | Molecular Biology Lavdovskaia, Elena Kolander, Elisa Steube, Emely Mai, Mandy Mong-Quyen Urlaub, Henning Richter-Dennerlein, Ricarda The human Obg protein GTPBP10 is involved in mitoribosomal biogenesis |
title | The human Obg protein GTPBP10 is involved in mitoribosomal biogenesis |
title_full | The human Obg protein GTPBP10 is involved in mitoribosomal biogenesis |
title_fullStr | The human Obg protein GTPBP10 is involved in mitoribosomal biogenesis |
title_full_unstemmed | The human Obg protein GTPBP10 is involved in mitoribosomal biogenesis |
title_short | The human Obg protein GTPBP10 is involved in mitoribosomal biogenesis |
title_sort | human obg protein gtpbp10 is involved in mitoribosomal biogenesis |
topic | Molecular Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6144781/ https://www.ncbi.nlm.nih.gov/pubmed/30085210 http://dx.doi.org/10.1093/nar/gky701 |
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