Acadian variant of Fanconi syndrome is caused by mitochondrial respiratory chain complex I deficiency due to a non-coding mutation in complex I assembly factor NDUFAF6
Language English Country England, Great Britain Media print-electronic
Document type Journal Article
PubMed
27466185
DOI
10.1093/hmg/ddw245
PII: ddw245
Knihovny.cz E-resources
- MeSH
- Alleles MeSH
- Adult MeSH
- Exome genetics MeSH
- Fanconi Syndrome genetics pathology MeSH
- Genetic Predisposition to Disease MeSH
- Heterozygote MeSH
- Homozygote MeSH
- Kidney metabolism pathology MeSH
- Middle Aged MeSH
- Humans MeSH
- Chromosome Mapping MeSH
- Mitochondrial Diseases genetics metabolism pathology MeSH
- Mitochondrial Proteins genetics MeSH
- Mitochondria metabolism pathology MeSH
- Mutation MeSH
- Lung metabolism pathology MeSH
- Electron Transport Complex I genetics MeSH
- Check Tag
- Adult MeSH
- Middle Aged MeSH
- Humans MeSH
- Male MeSH
- Female MeSH
- Publication type
- Journal Article MeSH
- Geographicals
- Canada MeSH
- Names of Substances
- Mitochondrial Proteins MeSH
- NDUFAF6 protein, human MeSH Browser
- Electron Transport Complex I MeSH
The Acadian variant of Fanconi Syndrome refers to a specific condition characterized by generalized proximal tubular dysfunction from birth, slowly progressive chronic kidney disease and pulmonary interstitial fibrosis. This condition occurs only in Acadians, a founder population in Nova Scotia, Canada. The genetic and molecular basis of this disease is unknown. We carried out whole exome and genome sequencing and found that nine affected individuals were homozygous for the ultra-rare non-coding variant chr8:96046914 T > C; rs575462405, whereas 13 healthy siblings were either heterozygotes or lacked the mutant allele. This variant is located in intron 2 of NDUFAF6 (NM_152416.3; c.298-768 T > C), 37 base pairs upstream from an alternative splicing variant in NDUFAF6 chr8:96046951 A > G; rs74395342 (c.298-731 A > G). NDUFAF6 encodes NADH:ubiquinone oxidoreductase complex assembly factor 6, also known as C8ORF38. We found that rs575462405-either alone or in combination with rs74395342-affects splicing and synthesis of NDUFAF6 isoforms. Affected kidney and lung showed specific loss of the mitochondria-located NDUFAF6 isoform and ultrastructural characteristics of mitochondrial dysfunction. Accordingly, affected tissues had defects in mitochondrial respiration and complex I biogenesis that were corrected with NDUFAF6 cDNA transfection. Our results demonstrate that the Acadian variant of Fanconi Syndrome results from mitochondrial respiratory chain complex I deficiency. This information may be used in the diagnosis and prevention of this disease in individuals and families of Acadian descent and broadens the spectrum of the clinical presentation of mitochondrial diseases, respiratory chain defects and defects of complex I specifically.
Institute of Physiology of the Czech Academy of Sciences Vídeňská 1083 Prague Czech Republic
IWK Health Center Halifax Nova Scotia Canada
Section on Nephrology Wake Forest School of Medicine Medical Center Blvd Winston Salem NC USA
References provided by Crossref.org
Misprocessing of α -Galactosidase A, Endoplasmic Reticulum Stress, and the Unfolded Protein Response
A Novel Monoallelic ALG5 Variant Causing Late-Onset ADPKD and Tubulointerstitial Fibrosis
Role of Mitochondrial Glycerol-3-Phosphate Dehydrogenase in Metabolic Adaptations of Prostate Cancer
Cytochrome c Oxidase Subunit 4 Isoform Exchange Results in Modulation of Oxygen Affinity
Outcomes of patient self-referral for the diagnosis of several rare inherited kidney diseases
Autosomal Dominant Tubulointerstitial Kidney Disease