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A small protein coded within the mitochondrial canonical gene nd4 regulates mitochondrial bioenergetics

BACKGROUND: Mitochondria have a central role in cellular functions, aging, and in certain diseases. They possess their own genome, a vestige of their bacterial ancestor. Over the course of evolution, most of the genes of the ancestor have been lost or transferred to the nucleus. In humans, the mtDNA...

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Autores principales: Kienzle, Laura, Bettinazzi, Stefano, Choquette, Thierry, Brunet, Marie, Khorami, Hajar Hosseini, Jacques, Jean-François, Moreau, Mathilde, Roucou, Xavier, Landry, Christian R., Angers, Annie, Breton, Sophie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10193809/
https://www.ncbi.nlm.nih.gov/pubmed/37198654
http://dx.doi.org/10.1186/s12915-023-01609-y
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author Kienzle, Laura
Bettinazzi, Stefano
Choquette, Thierry
Brunet, Marie
Khorami, Hajar Hosseini
Jacques, Jean-François
Moreau, Mathilde
Roucou, Xavier
Landry, Christian R.
Angers, Annie
Breton, Sophie
author_facet Kienzle, Laura
Bettinazzi, Stefano
Choquette, Thierry
Brunet, Marie
Khorami, Hajar Hosseini
Jacques, Jean-François
Moreau, Mathilde
Roucou, Xavier
Landry, Christian R.
Angers, Annie
Breton, Sophie
author_sort Kienzle, Laura
collection PubMed
description BACKGROUND: Mitochondria have a central role in cellular functions, aging, and in certain diseases. They possess their own genome, a vestige of their bacterial ancestor. Over the course of evolution, most of the genes of the ancestor have been lost or transferred to the nucleus. In humans, the mtDNA is a very small circular molecule with a functional repertoire limited to only 37 genes. Its extremely compact nature with genes arranged one after the other and separated by short non-coding regions suggests that there is little room for evolutionary novelties. This is radically different from bacterial genomes, which are also circular but much larger, and in which we can find genes inside other genes. These sequences, different from the reference coding sequences, are called alternatives open reading frames or altORFs, and they are involved in key biological functions. However, whether altORFs exist in mitochondrial protein-coding genes or elsewhere in the human mitogenome has not been fully addressed. RESULTS: We found a downstream alternative ATG initiation codon in the + 3 reading frame of the human mitochondrial nd4 gene. This newly characterized altORF encodes a 99-amino-acid-long polypeptide, MTALTND4, which is conserved in primates. Our custom antibody, but not the pre-immune serum, was able to immunoprecipitate MTALTND4 from HeLa cell lysates, confirming the existence of an endogenous MTALTND4 peptide. The protein is localized in mitochondria and cytoplasm and is also found in the plasma, and it impacts cell and mitochondrial physiology. CONCLUSIONS: Many human mitochondrial translated ORFs might have so far gone unnoticed. By ignoring mtaltORFs, we have underestimated the coding potential of the mitogenome. Alternative mitochondrial peptides such as MTALTND4 may offer a new framework for the investigation of mitochondrial functions and diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-023-01609-y.
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spelling pubmed-101938092023-05-19 A small protein coded within the mitochondrial canonical gene nd4 regulates mitochondrial bioenergetics Kienzle, Laura Bettinazzi, Stefano Choquette, Thierry Brunet, Marie Khorami, Hajar Hosseini Jacques, Jean-François Moreau, Mathilde Roucou, Xavier Landry, Christian R. Angers, Annie Breton, Sophie BMC Biol Research Article BACKGROUND: Mitochondria have a central role in cellular functions, aging, and in certain diseases. They possess their own genome, a vestige of their bacterial ancestor. Over the course of evolution, most of the genes of the ancestor have been lost or transferred to the nucleus. In humans, the mtDNA is a very small circular molecule with a functional repertoire limited to only 37 genes. Its extremely compact nature with genes arranged one after the other and separated by short non-coding regions suggests that there is little room for evolutionary novelties. This is radically different from bacterial genomes, which are also circular but much larger, and in which we can find genes inside other genes. These sequences, different from the reference coding sequences, are called alternatives open reading frames or altORFs, and they are involved in key biological functions. However, whether altORFs exist in mitochondrial protein-coding genes or elsewhere in the human mitogenome has not been fully addressed. RESULTS: We found a downstream alternative ATG initiation codon in the + 3 reading frame of the human mitochondrial nd4 gene. This newly characterized altORF encodes a 99-amino-acid-long polypeptide, MTALTND4, which is conserved in primates. Our custom antibody, but not the pre-immune serum, was able to immunoprecipitate MTALTND4 from HeLa cell lysates, confirming the existence of an endogenous MTALTND4 peptide. The protein is localized in mitochondria and cytoplasm and is also found in the plasma, and it impacts cell and mitochondrial physiology. CONCLUSIONS: Many human mitochondrial translated ORFs might have so far gone unnoticed. By ignoring mtaltORFs, we have underestimated the coding potential of the mitogenome. Alternative mitochondrial peptides such as MTALTND4 may offer a new framework for the investigation of mitochondrial functions and diseases. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12915-023-01609-y. BioMed Central 2023-05-18 /pmc/articles/PMC10193809/ /pubmed/37198654 http://dx.doi.org/10.1186/s12915-023-01609-y Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research Article
Kienzle, Laura
Bettinazzi, Stefano
Choquette, Thierry
Brunet, Marie
Khorami, Hajar Hosseini
Jacques, Jean-François
Moreau, Mathilde
Roucou, Xavier
Landry, Christian R.
Angers, Annie
Breton, Sophie
A small protein coded within the mitochondrial canonical gene nd4 regulates mitochondrial bioenergetics
title A small protein coded within the mitochondrial canonical gene nd4 regulates mitochondrial bioenergetics
title_full A small protein coded within the mitochondrial canonical gene nd4 regulates mitochondrial bioenergetics
title_fullStr A small protein coded within the mitochondrial canonical gene nd4 regulates mitochondrial bioenergetics
title_full_unstemmed A small protein coded within the mitochondrial canonical gene nd4 regulates mitochondrial bioenergetics
title_short A small protein coded within the mitochondrial canonical gene nd4 regulates mitochondrial bioenergetics
title_sort small protein coded within the mitochondrial canonical gene nd4 regulates mitochondrial bioenergetics
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10193809/
https://www.ncbi.nlm.nih.gov/pubmed/37198654
http://dx.doi.org/10.1186/s12915-023-01609-y
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