| Literature DB >> 30010796 |
Juliana Gurgel-Giannetti1, David S Lynch2,3, Anderson Rodrigues Brandão de Paiva4, Leandro Tavares Lucato5, Guilherme Yamamoto6, Christer Thomsen7, Somsuvro Basu8, Fernando Freua4, Alexandre Varella Giannetti9, Bruno Della Ripa de Assis4, Mara Dell Ospedale Ribeiro4, Isabella Barcelos4, Katiane Sayão Souza4, Fernanda Monti4, Uirá Souto Melo6, Simone Amorim4, Leonardo G L Silva6, Lúcia Inês Macedo-Souza6, Angela M Vianna-Morgante6, Michio Hirano10, Marjo S Van der Knaap11, Roland Lill8,12, Mariz Vainzof6, Anders Oldfors7, Henry Houlden2,3, Fernando Kok4,6.
Abstract
Defects in iron-sulphur [Fe-S] cluster biogenesis are increasingly recognized as causing neurological disease. Mutations in a number of genes that encode proteins involved in mitochondrial [Fe-S] protein assembly lead to complex neurological phenotypes. One class of proteins essential in the early cluster assembly are ferredoxins. FDX2 is ubiquitously expressed and is essential in the de novo formation of [2Fe-2S] clusters in humans. We describe and genetically define a novel complex neurological syndrome identified in two Brazilian families, with a novel homozygous mutation in FDX2. Patients were clinically evaluated, underwent MRI, nerve conduction studies, EMG and muscle biopsy. To define the genetic aetiology, a combination of homozygosity mapping and whole exome sequencing was performed. We identified six patients from two apparently unrelated families with autosomal recessive inheritance of a complex neurological phenotype involving optic atrophy and nystagmus developing by age 3, followed by myopathy and recurrent episodes of cramps, myalgia and muscle weakness in the first or second decade of life. Sensory-motor axonal neuropathy led to progressive distal weakness. MRI disclosed a reversible or partially reversible leukoencephalopathy. Muscle biopsy demonstrated an unusual pattern of regional succinate dehydrogenase and cytochrome c oxidase deficiency with iron accumulation. The phenotype was mapped in both families to the same homozygous missense mutation in FDX2 (c.431C > T, p.P144L). The deleterious effect of the mutation was validated by real-time reverse transcription polymerase chain reaction and western blot analysis, which demonstrated normal expression of FDX2 mRNA but severely reduced expression of FDX2 protein in muscle tissue. This study describes a novel complex neurological phenotype with unusual MRI and muscle biopsy features, conclusively mapped to a mutation in FDX2, which encodes a ubiquitously expressed mitochondrial ferredoxin essential for early [Fe-S] cluster biogenesis.Entities:
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Year: 2018 PMID: 30010796 PMCID: PMC6061701 DOI: 10.1093/brain/awy172
Source DB: PubMed Journal: Brain ISSN: 0006-8950 Impact factor: 13.501