2. Academic Validation
  3. Exome sequencing identifies NFS1 deficiency in a novel Fe-S cluster disease, infantile mitochondrial complex II/III deficiency

Exome sequencing identifies NFS1 deficiency in a novel Fe-S cluster disease, infantile mitochondrial complex II/III deficiency

  • Mol Genet Genomic Med. 2014 Jan;2(1):73-80. doi: 10.1002/mgg3.46.
Sali M K Farhan 1,  Jian Wang 2,  John F Robinson 2,  Piya Lahiry 2,  Victoria M Siu 3,  Chitra Prasad 3,  Jonathan B Kronick 4,  David A Ramsay 5,  C Anthony Rupar 3,  Robert A Hegele 1
Affiliations

Affiliations

  • 1 Robarts Research Institute, Schulich School of Medicine and Dentistry, Western University London, Ontario, N6A 5K8, Canada ; Department of Biochemistry Schulich School of Medicine and Dentistry, Western University London, Ontario, N6A 5C1, Canada.
  • 2 Robarts Research Institute, Schulich School of Medicine and Dentistry, Western University London, Ontario, N6A 5K8, Canada.
  • 3 Department of Biochemistry Schulich School of Medicine and Dentistry, Western University London, Ontario, N6A 5C1, Canada ; Medical Genetics Program Department of Pediatrics, London Health Sciences Centre London, Ontario, N6C 2V5, Canada ; Children's Health Research Institute, London Health Sciences Centre London, Ontario, N6C 2V5, Canada.
  • 4 Division of Clinical and Metabolic Genetics The Hospital for Sick Children Department of Pediatrics, University of Toronto Toronto, Ontario, M5G 1X8, Canada.
  • 5 Department of Pathology, London Health Sciences Centre London, Ontario, N6A 5A5, Canada.
PMID: 24498631 DOI: 10.1002/mgg3.46
Abstract

Iron-sulfur (Fe-S) clusters are a class of highly conserved and ubiquitous prosthetic groups with unique chemical properties that allow the proteins that contain them, Fe-S proteins, to assist in various key biochemical pathways. Mutations in Fe-S proteins often disrupt Fe-S cluster assembly leading to a spectrum of severe disorders such as Friedreich's ataxia or iron-sulfur cluster assembly Enzyme (ISCU) myopathy. Herein, we describe infantile mitochondrial complex II/III deficiency, a novel autosomal recessive mitochondrial disease characterized by lactic acidemia, hypotonia, respiratory chain complex II and III deficiency, multisystem organ failure and abnormal mitochondria. Through autozygosity mapping, exome sequencing, in silico analyses, population studies and functional tests, we identified c.215G>A, p.Arg72Gln in NFS1 as the likely causative mutation. We describe the first disease in man likely caused by deficiency in NFS1, a cysteine desulfurase that is implicated in respiratory chain function and iron maintenance by initiating Fe-S cluster biosynthesis. Our results further demonstrate the importance of sufficient NFS1 expression in human physiology.

Keywords

Autozygosity mapping; Fe-S proteins; NFS1; mitochondrial complex deficiency; whole-exome sequencing..

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