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Mitochondrial transcription and translation: overview

Mitochondria are the major source of ATP in the cell. Five multi-subunit complexes in the inner membrane of the organelle are involved in the oxidative phosphorylation required for ATP production. Thirteen subunits of these complexes are encoded by the mitochondrial genome often referred to as mtDNA...

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Detalles Bibliográficos
Autores principales: D’Souza, Aaron R., Minczuk, Michal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Portland Press Ltd. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6056719/
https://www.ncbi.nlm.nih.gov/pubmed/30030363
http://dx.doi.org/10.1042/EBC20170102
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author D’Souza, Aaron R.
Minczuk, Michal
author_facet D’Souza, Aaron R.
Minczuk, Michal
author_sort D’Souza, Aaron R.
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description Mitochondria are the major source of ATP in the cell. Five multi-subunit complexes in the inner membrane of the organelle are involved in the oxidative phosphorylation required for ATP production. Thirteen subunits of these complexes are encoded by the mitochondrial genome often referred to as mtDNA. For this reason, the expression of mtDNA is vital for the assembly and functioning of the oxidative phosphorylation complexes. Defects of the mechanisms regulating mtDNA gene expression have been associated with deficiencies in assembly of these complexes, resulting in mitochondrial diseases. Recently, numerous factors involved in these processes have been identified and characterized leading to a deeper understanding of the mechanisms that underlie mitochondrial diseases.
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spelling pubmed-60567192018-08-08 Mitochondrial transcription and translation: overview D’Souza, Aaron R. Minczuk, Michal Essays Biochem Review Articles Mitochondria are the major source of ATP in the cell. Five multi-subunit complexes in the inner membrane of the organelle are involved in the oxidative phosphorylation required for ATP production. Thirteen subunits of these complexes are encoded by the mitochondrial genome often referred to as mtDNA. For this reason, the expression of mtDNA is vital for the assembly and functioning of the oxidative phosphorylation complexes. Defects of the mechanisms regulating mtDNA gene expression have been associated with deficiencies in assembly of these complexes, resulting in mitochondrial diseases. Recently, numerous factors involved in these processes have been identified and characterized leading to a deeper understanding of the mechanisms that underlie mitochondrial diseases. Portland Press Ltd. 2018-07-20 /pmc/articles/PMC6056719/ /pubmed/30030363 http://dx.doi.org/10.1042/EBC20170102 Text en © 2018 The Author(s). http://creativecommons.org/licenses/by/4.0/This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (http://creativecommons.org/licenses/by/4.0/) .
spellingShingle Review Articles
D’Souza, Aaron R.
Minczuk, Michal
Mitochondrial transcription and translation: overview
title Mitochondrial transcription and translation: overview
title_full Mitochondrial transcription and translation: overview
title_fullStr Mitochondrial transcription and translation: overview
title_full_unstemmed Mitochondrial transcription and translation: overview
title_short Mitochondrial transcription and translation: overview
title_sort mitochondrial transcription and translation: overview
topic Review Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6056719/
https://www.ncbi.nlm.nih.gov/pubmed/30030363
http://dx.doi.org/10.1042/EBC20170102
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