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Closed Access item Coenzyme Q10 deficiencies in neuromuscular diseases

Authors:Artuch, Rafael
Salviati, Leonardo
Jackson, Sandra
Navas, Plácido
Keywords:Mitochondria, Coenzyme Q10 deficiency, Neuromuscular diseases, Prenyldiphosphate
Issue Date:2009
Publisher:Springer
Citation:Inherited neuromuscular diseases: 117-128 (2009)
Series/Report no.:Advances in Experimental Medicine and Biology
652
Abstract:Coenzyme Q (CoQ) is an esssential component of the respiratory chain but also participates in other mitochondrial functions such as regulation of the transition pore and uncoupling proteins. Furthermore, this compound is a specific substrate for enzymes of the fatty acids β-oxidation pathway and pyrimidine nucleotide biosynthesis. Furthermore, CoQ is an antioxidant that acts in all cellular membranes and lipoproteins. A complex of a least ten nuclear (COQ) genes encoded proteins synthesis CoQ but its regulation is unknown. Since 1989, a growing number of patients with multsystemic mitochondrial disorders and neuromuscular disorders showing deficiencies of CoQ have been identified. CoQ deficiency caused by mutation(s) in any of the COQ genes in designated primary deficiency. Other patients have displayed other genetic defects independent on the CoQ biosynthesis pathway, and are considered to have secondary deficiencies. This review updates the clinical and molecular aspects of both types of CoQ deficiencies and proposes new approaches to understanding their molecular bases.
Description:páginas, 2 figuras, 1 tabla. Editado por Carmen Espinós, Vicente Felipo y Francesc Palau.
Publisher version (URL):http://dx.doi.org/10.1007/978-90-481-2813-6
URI:http://hdl.handle.net/10261/41680
ISBN:978-90-481-2812-9
ISSN:0065-2598
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Appears in Collections:(CABD) Libros y partes de libros

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