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Mitochondrial transcription and translation: overview
Author(s) -
Aaron R. D’Souza,
Michal Minczuk
Publication year - 2018
Publication title -
essays in biochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.351
H-Index - 66
eISSN - 1744-1358
pISSN - 0071-1365
DOI - 10.1042/ebc20170102
Subject(s) - mitochondrial dna , mitochondrion , oxidative phosphorylation , microbiology and biotechnology , biology , inner mitochondrial membrane , organelle , atp–adp translocase , transcription (linguistics) , protein subunit , mitochondrial fusion , gene , dnaja3 , translation (biology) , genetics , biochemistry , messenger rna , linguistics , philosophy
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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