Literature DB >> 30010796

A novel complex neurological phenotype due to a homozygous mutation in FDX2.

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.

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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


  33 in total

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Authors:  Thomas D Schmittgen; Kenneth J Livak
Journal:  Nat Protoc       Date:  2008       Impact factor: 13.491

2.  Functional reconstitution of mitochondrial Fe/S cluster synthesis on Isu1 reveals the involvement of ferredoxin.

Authors:  Holger Webert; Sven-Andreas Freibert; Angelo Gallo; Torsten Heidenreich; Uwe Linne; Stefan Amlacher; Ed Hurt; Ulrich Mühlenhoff; Lucia Banci; Roland Lill
Journal:  Nat Commun       Date:  2014-10-31       Impact factor: 14.919

3.  Exomic variants of an elderly cohort of Brazilians in the ABraOM database.

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Journal:  Hum Mutat       Date:  2017-05-03       Impact factor: 4.878

Review 4.  Mammalian Fe-S cluster biogenesis and its implication in disease.

Authors:  Lena K Beilschmidt; Hélène M Puccio
Journal:  Biochimie       Date:  2014-01-17       Impact factor: 4.079

5.  Humans possess two mitochondrial ferredoxins, Fdx1 and Fdx2, with distinct roles in steroidogenesis, heme, and Fe/S cluster biosynthesis.

Authors:  Alex D Sheftel; Oliver Stehling; Antonio J Pierik; Hans-Peter Elsässer; Ulrich Mühlenhoff; Holger Webert; Anna Hobler; Frank Hannemann; Rita Bernhardt; Roland Lill
Journal:  Proc Natl Acad Sci U S A       Date:  2010-06-14       Impact factor: 11.205

Review 6.  Iron-sulfur clusters: nature's modular, multipurpose structures.

Authors:  H Beinert; R H Holm; E Münck
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9.  Brain white matter oedema due to ClC-2 chloride channel deficiency: an observational analytical study.

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Journal:  Lancet Neurol       Date:  2013-05-22       Impact factor: 44.182

10.  Biochemical Analyses of Human Iron-Sulfur Protein Biogenesis and of Related Diseases.

Authors:  Oliver Stehling; Viktoria D Paul; Janina Bergmann; Somsuvro Basu; Roland Lill
Journal:  Methods Enzymol       Date:  2017-12-06       Impact factor: 1.600

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  11 in total

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4.  Expression pattern of mitochondrial respiratory chain enzymes in skeletal muscle of patients with mitochondrial myopathy associated with the homoplasmic m.14674T>C variant.

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5.  Sex differences in the genetic architecture of depression.

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6.  A novel remitting leukodystrophy associated with a variant in FBP2.

Authors:  Agnieszka Gizak; Susann Diegmann; Steffi Dreha-Kulaczewski; Janusz Wiśniewski; Przemysław Duda; Andreas Ohlenbusch; Brenda Huppke; Marco Henneke; Wolfgang Höhne; Janine Altmüller; Holger Thiele; Peter Nürnberg; Dariusz Rakus; Jutta Gärtner; Peter Huppke
Journal:  Brain Commun       Date:  2021-03-11

7.  FDX2 and ISCU Gene Variations Lead to Rhabdomyolysis With Distinct Severity and Iron Regulation.

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8.  GLRX5-associated [Fe-S] cluster biogenesis disorder: further characterisation of the neurological phenotype and long-term outcome.

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9.  Imaging Patterns Characterizing Mitochondrial Leukodystrophies.

Authors:  S D Roosendaal; T van de Brug; C A P F Alves; S Blaser; A Vanderver; N I Wolf; M S van der Knaap
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Review 10.  Down the Iron Path: Mitochondrial Iron Homeostasis and Beyond.

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