Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia

R. Virgilio, D. Ronchi, G. M. Hadjigeorgiou, A. Bordoni, F. Saladino, M. Moggio, L. Adobbati, D. Kafetsouli, E. Tsironi, S. Previtali, A. Papadimitriou, N. Bresolin, G. P. Comi

Research output: Contribution to journalArticle

38 Citations (Scopus)

Abstract

Multiple deletions of mitochondrial DNA (mtDNA) are associated with different mitochondrial disorders inherited as autosomal dominant and recessive traits. Causative mutations have been found in five genes, mainly involved in mtDNA replication and stability. They include POLG1, the gene encoding the catalytic subunit of mtDNA polymerase (polγ), POLG2 encoding its accessory subunit, ANT1 coding the adenine nucleotide translocator and PEO1 which codes for Twinkle, the mitochondrial helicase. Finally OPA1 missense mutations are involved in phenotypes presenting optic atrophy as a major feature. To define the relative contribution of POLG1, POLG2, ANT1 and PEO1 genes to the mtDNA multiple deletion syndromes, we analysed them in a cohort of 67 probands showing accumulation of multiple mtDNA deletions in muscle. The patients were predominantly affected with a mitochondrial myopathy with or without progressive external ophthalmoplegia (PEO). Genetic analysis revealed that 1) PEO1 has a major role in determining familial PEO, since it accounts for 26.8% of familial cases, followed by ANT1 (14.6%) and POLG1 (9.8%); 2) no mutations in any of the known genes were found in 53.7% of probands of this series. Six novel missense mutations contributing to the mutational load of PEO1 gene (p.R334P, p.W315S, p. S426N, p.W474S, p.F478I, p.E479K) were associated with an adult onset PEO phenotype.

Original languageEnglish
Pages (from-to)1384-1391
Number of pages8
JournalJournal of Neurology
Volume255
Issue number9
DOIs
Publication statusPublished - Sep 2008

Fingerprint

Chronic Progressive External Ophthalmoplegia
Mitochondrial DNA
Mutation
Genes
Missense Mutation
Mitochondrial Myopathies
Phenotype
Optic Atrophy
Mitochondrial Diseases
Adenine Nucleotides
DNA-Directed DNA Polymerase
DNA Replication
Catalytic Domain
Muscles

Keywords

  • mtDNA deletions
  • Progressive external ophthalmoplegia

ASJC Scopus subject areas

  • Clinical Neurology
  • Neurology

Cite this

Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia. / Virgilio, R.; Ronchi, D.; Hadjigeorgiou, G. M.; Bordoni, A.; Saladino, F.; Moggio, M.; Adobbati, L.; Kafetsouli, D.; Tsironi, E.; Previtali, S.; Papadimitriou, A.; Bresolin, N.; Comi, G. P.

In: Journal of Neurology, Vol. 255, No. 9, 09.2008, p. 1384-1391.

Research output: Contribution to journalArticle

Virgilio, R, Ronchi, D, Hadjigeorgiou, GM, Bordoni, A, Saladino, F, Moggio, M, Adobbati, L, Kafetsouli, D, Tsironi, E, Previtali, S, Papadimitriou, A, Bresolin, N & Comi, GP 2008, 'Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia', Journal of Neurology, vol. 255, no. 9, pp. 1384-1391. https://doi.org/10.1007/s00415-008-0926-3
Virgilio, R. ; Ronchi, D. ; Hadjigeorgiou, G. M. ; Bordoni, A. ; Saladino, F. ; Moggio, M. ; Adobbati, L. ; Kafetsouli, D. ; Tsironi, E. ; Previtali, S. ; Papadimitriou, A. ; Bresolin, N. ; Comi, G. P. / Novel Twinkle (PEO1) gene mutations in mendelian progressive external ophthalmoplegia. In: Journal of Neurology. 2008 ; Vol. 255, No. 9. pp. 1384-1391.
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AU - Saladino, F.

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AU - Adobbati, L.

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AU - Tsironi, E.

AU - Previtali, S.

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