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Mutations in COQ2 in Familial and Sporadic Multiple-System Atrophy
- Source :
- The New England journal of medicine 369(3), 233-244 (2013). doi:10.1056/NEJMoa1212115
- Publication Year :
- 2013
- Publisher :
- Massachusetts Medical Society, 2013.
-
Abstract
- Multiple-system atrophy is an intractable neurodegenerative disease characterized by autonomic failure in addition to various combinations of parkinsonism, cerebellar ataxia, and pyramidal dysfunction. Although multiple-system atrophy is widely considered to be a nongenetic disorder, we previously identified multiplex families with this disease, which indicates the involvement of genetic components.In combination with linkage analysis, we performed whole-genome sequencing of a sample obtained from a member of a multiplex family in whom multiple-system atrophy had been diagnosed on autopsy. We also performed mutational analysis of samples from members of five other multiplex families and from a Japanese series (363 patients and two sets of controls, one of 520 persons and one of 2383 persons), a European series (223 patients and 315 controls), and a North American series (172 patients and 294 controls). On the basis of these analyses, we used a yeast complementation assay and measured enzyme activity of parahydroxybenzoate-polyprenyl transferase. This enzyme is encoded by the gene COQ2 and is essential for the biosynthesis of coenzyme Q10. Levels of coenzyme Q10 in lymphoblastoid cells and brain tissue were measured on high-performance liquid chromatography.We identified a homozygous mutation (M78V-V343A/M78V-V343A) and compound heterozygous mutations (R337X/V343A) in COQ2 in two multiplex families. Furthermore, we found that a common variant (V343A) and multiple rare variants in COQ2, all of which are functionally impaired, are associated with sporadic multiple-system atrophy. The V343A variant was exclusively observed in the Japanese population.Functionally impaired variants of COQ2 were associated with an increased risk of multiple-system atrophy in multiplex families and patients with sporadic disease, providing evidence of a role of impaired COQ2 activities in the pathogenesis of this disease. (Funded by the Japan Society for the Promotion of Science and others.).
- Subjects :
- Male
Genetic Linkage
Ubiquinone
DNA Mutational Analysis
Cell Line
World Wide Web
Atrophy
coenzyme Q10
Humans
Medicine
4-hydroxybenzoate polyprenyltransferase
ddc:610
analysis [Ubiquinone]
analogs & derivatives [Ubiquinone]
Brain Chemistry
Thesaurus (information retrieval)
Alkyl and Aryl Transferases
business.industry
General Medicine
genetics [Alkyl and Aryl Transferases]
medicine.disease
Pedigree
Mutation
Female
genetics [Multiple System Atrophy]
business
Subjects
Details
- ISSN :
- 15334406 and 00284793
- Volume :
- 369
- Database :
- OpenAIRE
- Journal :
- New England Journal of Medicine
- Accession number :
- edsair.doi.dedup.....278e847779e0f61aaacdd8bf6c5654c5
- Full Text :
- https://doi.org/10.1056/nejmoa1212115