Novel mutations of ND genes in complex I deficiency associated with mitochondrial encephalopathy

Edoardo Malfatti, Marianna Bugiani, Federica Invernizzi, C. F M De Souza, Laura Farina, Franco Carrara, Eleonora Lamantea, Carlo Antozzi, Paolo Confalonieri, Maria Teresa Sanseverino, Roberto Giugliani, Graziella Uziel, Massimo Zeviani

Research output: Contribution to journalArticle

79 Citations (Scopus)

Abstract

Isolated Complex I (CI) deficiency, the most frequent cause of mitochondrial disease, is a clinically and genetically heterogeneous condition. Complex I is a giant multiheteromeric enzyme composed of seven ND subunits encoded by mitochondrial DNA (mtDNA) genes, and at least 38 subunits encoded by nuclear genes. To establish the contribution to human mitochondrial encephalopathy of ND versus nuclear gene mutations, we have been undertaking a systematic analysis of CI genes in a cohort of 46 adult and paediatric patients with biochemically defined CI defect. Sequence analysis of the entire mtDNA let us identify six patients with mutations in ND genes. The clinical presentations varied, from infantile Leigh syndrome, to childhood MELAS, to adult-onset encephalopathic syndromes of variable severity. Three of the mutations were not previously reported (3481G > A, 14600G > A and 13063G > A, in ND1, ND6 and ND5 genes, respectively) and were further investigated in mutant transmitochondrial cybrids. Tight correlation between mutation load and decrease in CI activity was observed in each of the three mutant cybrid lines, supporting the pathogenic role of the novel mutations. Structural studies on mutant cybrids showed impaired assembly or reduced stability of the holoenzyme complex. In our experience ND gene mutations are relatively common in CI-defective mitochondrial encephalopathy of both children and adults.

Original languageEnglish
Pages (from-to)1894-1904
Number of pages11
JournalBrain
Volume130
Issue number7
DOIs
Publication statusPublished - Jul 2007

Fingerprint

Mutation
Genes
Mitochondrial DNA
MELAS Syndrome
Leigh Disease
Mitochondrial Diseases
Holoenzymes
Mitochondrial Genes
Sequence Analysis
Mitochondrial encephalopathy
Pediatrics
Enzymes

Keywords

  • Assembly
  • Complex I deficiency
  • Mitochondrial encephalomyopathy
  • mtDNA mutation

ASJC Scopus subject areas

  • Medicine(all)
  • Neuroscience(all)

Cite this

Malfatti, E., Bugiani, M., Invernizzi, F., De Souza, C. F. M., Farina, L., Carrara, F., ... Zeviani, M. (2007). Novel mutations of ND genes in complex I deficiency associated with mitochondrial encephalopathy. Brain, 130(7), 1894-1904. https://doi.org/10.1093/brain/awm114

Novel mutations of ND genes in complex I deficiency associated with mitochondrial encephalopathy. / Malfatti, Edoardo; Bugiani, Marianna; Invernizzi, Federica; De Souza, C. F M; Farina, Laura; Carrara, Franco; Lamantea, Eleonora; Antozzi, Carlo; Confalonieri, Paolo; Sanseverino, Maria Teresa; Giugliani, Roberto; Uziel, Graziella; Zeviani, Massimo.

In: Brain, Vol. 130, No. 7, 07.2007, p. 1894-1904.

Research output: Contribution to journalArticle

Malfatti, E, Bugiani, M, Invernizzi, F, De Souza, CFM, Farina, L, Carrara, F, Lamantea, E, Antozzi, C, Confalonieri, P, Sanseverino, MT, Giugliani, R, Uziel, G & Zeviani, M 2007, 'Novel mutations of ND genes in complex I deficiency associated with mitochondrial encephalopathy', Brain, vol. 130, no. 7, pp. 1894-1904. https://doi.org/10.1093/brain/awm114
Malfatti E, Bugiani M, Invernizzi F, De Souza CFM, Farina L, Carrara F et al. Novel mutations of ND genes in complex I deficiency associated with mitochondrial encephalopathy. Brain. 2007 Jul;130(7):1894-1904. https://doi.org/10.1093/brain/awm114
Malfatti, Edoardo ; Bugiani, Marianna ; Invernizzi, Federica ; De Souza, C. F M ; Farina, Laura ; Carrara, Franco ; Lamantea, Eleonora ; Antozzi, Carlo ; Confalonieri, Paolo ; Sanseverino, Maria Teresa ; Giugliani, Roberto ; Uziel, Graziella ; Zeviani, Massimo. / Novel mutations of ND genes in complex I deficiency associated with mitochondrial encephalopathy. In: Brain. 2007 ; Vol. 130, No. 7. pp. 1894-1904.
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abstract = "Isolated Complex I (CI) deficiency, the most frequent cause of mitochondrial disease, is a clinically and genetically heterogeneous condition. Complex I is a giant multiheteromeric enzyme composed of seven ND subunits encoded by mitochondrial DNA (mtDNA) genes, and at least 38 subunits encoded by nuclear genes. To establish the contribution to human mitochondrial encephalopathy of ND versus nuclear gene mutations, we have been undertaking a systematic analysis of CI genes in a cohort of 46 adult and paediatric patients with biochemically defined CI defect. Sequence analysis of the entire mtDNA let us identify six patients with mutations in ND genes. The clinical presentations varied, from infantile Leigh syndrome, to childhood MELAS, to adult-onset encephalopathic syndromes of variable severity. Three of the mutations were not previously reported (3481G > A, 14600G > A and 13063G > A, in ND1, ND6 and ND5 genes, respectively) and were further investigated in mutant transmitochondrial cybrids. Tight correlation between mutation load and decrease in CI activity was observed in each of the three mutant cybrid lines, supporting the pathogenic role of the novel mutations. Structural studies on mutant cybrids showed impaired assembly or reduced stability of the holoenzyme complex. In our experience ND gene mutations are relatively common in CI-defective mitochondrial encephalopathy of both children and adults.",
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