Difference between revisions of "Pecina 2004 Physiol Res"
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{{Labeling | {{Labeling | ||
|area=Respiration, | |area=Respiration, mtDNA;mt-genetics, mt-Medicine, Patients | ||
|organism=Human | |organism=Human | ||
|tissues=Skeletal muscle | |tissues=Skeletal muscle | ||
|model cell lines=Fibroblast | |model cell lines=Fibroblast | ||
|enzymes=Complex IV; Cytochrome c Oxidase | |enzymes=Complex IV; Cytochrome c Oxidase | ||
|diseases= | |diseases=Inherited | ||
|instruments=Oxygraph-2k | |instruments=Oxygraph-2k | ||
|discipline=Mitochondrial Physiology | |discipline=Mitochondrial Physiology | ||
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Revision as of 16:24, 11 August 2013
Pecina P, Houstkova H, Hansikova H, Zeman J, Houstek J (2004) Genetic defects of cytochrome c oxidase assembly. Physiol Res 53 Suppl 1: S213-223. |
Pecina P, Houstkova H, Hansikova H, Zeman J, Houstek J (2004) Physiol Res
Abstract: Cytochrome c oxidase (COX), the terminal enzyme of the mitochondrial respiratory chain, is one of the key functional and regulatory sites of the mammalian energy metabolism. Owing to the importance of the enzyme, pathogenetic mutations affecting COX frequently result in severe, often fatal metabolic disorders. No satisfactory therapy is currently available so that the treatment remains largely symptomatic and does not improve the course of the disease. While only few genetic defects of COX are caused by mutations in mitochondrial genome, during the last five years a large number of pathogenetic mutations in nuclear genes have been discovered. All these mutations are located in genes encoding COX-specific assembly proteins including SURF1, SCO1, SCO2, COX10, and COX15. Despite the identification of increasing number of mutations, their precise etiopathogenetic mechanisms, which are necessary for the development of future therapeutic protocols, still remain to be elucidated. This review summarizes recent developments, including our efforts in elucidation of the molecular basis of human mitochondrial diseases due to specific defects of COX with special focus on SURF1 assembly protein. β’ Keywords: Cytochrome c oxidase, SURF1, Leigh syndrome, Mitochondrial disorders
β’ O2k-Network Lab: CZ_Prague_Houstek J, CZ_Prague_Zeman J, CZ Prague Bioenergetics
Labels: MiParea: Respiration, mtDNA;mt-genetics, mt-Medicine, Patients
Pathology: Inherited
Organism: Human Tissue;cell: Skeletal muscle
Enzyme: Complex IV; Cytochrome c Oxidase"Complex IV; Cytochrome c Oxidase" is not in the list (Adenine nucleotide translocase, Complex I, Complex II;succinate dehydrogenase, Complex III, Complex IV;cytochrome c oxidase, Complex V;ATP synthase, Inner mt-membrane transporter, Marker enzyme, Supercomplex, TCA cycle and matrix dehydrogenases, ...) of allowed values for the "Enzyme" property.
HRR: Oxygraph-2k