Mitochondrial Transcription and Translation: Overview
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Authors
D'Souza, aaron
Minczuk, M
Publication Date
2018-07-20Journal Title
Essays in Biochemistry
ISSN
0071-1365
Publisher
Portland Press, Ltd.
Volume
62
Pages
309-320
Language
eng
Type
Article
This Version
VoR
Metadata
Show full item recordCitation
D'Souza, a., & Minczuk, M. (2018). Mitochondrial Transcription and Translation: Overview. Essays in Biochemistry, 62 309-320. https://doi.org/10.1042/EBC20170102
Abstract
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 characterised leading to a deeper understanding of the mechanisms that underlie mitochondrial diseases.
Keywords
mitochondria, translation, trascription, Adenosine Triphosphate, DNA, Mitochondrial, Humans, Mitochondria, Mitochondrial Diseases, Oxidative Phosphorylation, Protein Biosynthesis, RNA, Messenger, RNA, Transfer, RNA, Transfer, Amino Acyl, Ribosomes, Transcription, Genetic
Sponsorship
Medical Research Council (MC_U105697135)
Medical Research Council (MC_UU_00015/4)
Embargo Lift Date
2100-01-01
Identifiers
External DOI: https://doi.org/10.1042/EBC20170102
This record's URL: https://www.repository.cam.ac.uk/handle/1810/283188
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