Primary Coenzyme Q deficiency Due to Novel ADCK3 Variants, Studies in Fibroblasts and Review of Literature. View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2019-04-09

AUTHORS

Adel Shalata, Michael Edery, Clair Habib, Jacob Genizi, Mohammad Mahroum, Lama Khalaily, Nurit Assaf, Idan Segal, Hoda Abed El Rahim, Hana Shapira, Danielle Urian, Shay Tzur, Liza Douiev, Ann Saada

ABSTRACT

Primary deficiency of coenzyme Q10 (CoQ10 ubiquinone), is classified as a mitochondrial respiratory chain disorder with phenotypic variability. The clinical manifestation may involve one or multiple tissue with variable severity and presentation may range from infancy to late onset. ADCK3 gene mutations are responsible for the most frequent form of hereditary CoQ10 deficiency (Q10 deficiency-4 OMIM #612016) which is mainly associated with autosomal recessive spinocerebellar ataxia (ARCA2, SCAR9). Here we provide the clinical, biochemical and genetic investigation for unrelated three nuclear families presenting an autosomal form of Spino-Cerebellar Ataxia due to novel mutations in the ADCK3 gene. Using next generation sequence technology we identified a homozygous Gln343Ter mutation in one family with severe, early onset of the disease and compound heterozygous mutations of Gln343Ter and Ser608Phe in two other families with variable manifestations. Biochemical investigation in fibroblasts showed decreased activity of the CoQ dependent mitochondrial respiratory chain enzyme succinate cytochrome c reductase (complex II + III). Exogenous CoQ slightly improved enzymatic activity, ATP production and decreased oxygen free radicals in some of the patient's cells. Our results are presented in comparison to previously reported mutations and expanding the clinical, molecular and biochemical spectrum of ADCK3 related CoQ10 deficiencies. More... »

Identifiers

URI

http://scigraph.springernature.com/pub.10.1007/s11064-019-02786-5

DOI

http://dx.doi.org/10.1007/s11064-019-02786-5

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1113328066

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/30968303


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