Multiple Deletions in Mitochondrial DNA in a Patient with Progressive External Ophthalmoplegia, Leukoencephalopathy and Hypogonadism

被引:6
|
作者
Ohnuki, Yuko [1 ,2 ]
Takahashi, Kazumi [2 ,3 ]
Iijima, Eri [4 ]
Takahashi, Wakoh [4 ]
Suzuki, Shingo [1 ]
Ozaki, Yuki [1 ]
Kitao, Ruriko
Mihara, Masatoshi [5 ]
Ishihara, Tadayuki [5 ]
Nakamura, Michiyo [6 ]
Sawano, Yoshie [6 ]
Goto, Yu-ichi [6 ]
Izumi, Shunichiro [2 ,3 ]
Kulski, Jerzy K. [1 ,7 ]
Shiina, Takashi [1 ]
Takizawa, Shunya [4 ]
机构
[1] Tokai Univ, Sch Med, Dept Mol Life Sci Basic Med Sci & Mol Med, Hiratsuka, Kanagawa 25912, Japan
[2] Tokai Univ Hosp, Dept Clin Genet, Hiratsuka, Kanagawa, Japan
[3] Tokai Univ, Sch Med, Dept Obstet & Gynecol, Hiratsuka, Kanagawa 25912, Japan
[4] Tokai Univ, Sch Med, Dept Internal Med, Div Neurol, Hiratsuka, Kanagawa 25912, Japan
[5] Natl Hakone Hosp, Dept Neurol, Odawara, Kanagawa, Japan
[6] Natl Ctr Neurol & Psychiat, Dept Mental Retardat & Birth Defect Res, Tokyo, Japan
[7] Univ Western Australia, Ctr Forens Sci, Nedlands, WA 6009, Australia
关键词
mitochondrial DNA (mtDNA); multiple deletion; progressive external ophthalmoplegia (PEO); hypogonadism; leukoencephalopathy; MUTATIONS;
D O I
10.2169/internalmedicine.53.1320
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Progressive external ophthalmoplegia (PEO) is one of a number of major types of mitochondrial disorders. Most sporadic PEO patients have a heteroplasmic large deletion of mitochondrial DNA (mtDNA) in the mitochondria in skeletal muscles. We herein analyzed mtDNA deletions using sub-cloning and Sanger sequencing of PCR products in a 31-year-old Japanese man with multiple symptoms, including PEO, muscle weakness, hearing loss, leukoencephalopathy and hypogonadism. A large number of multiple deletions was detected, as well as four kinds of deletion breakpoints identified in different locations, including m.3347_12322, m.5818_13964, m.5829_13964 and m.5837_13503.
引用
收藏
页码:1365 / 1369
页数:5
相关论文
共 50 条
  • [31] Deletions of the mitochondrial DNA associated to chronic progressive external ophthalmoplegia with ragged-red fibers in 2 Brazilian patients
    Carod-Artal, FJ
    López-Gallardo, E
    Solano, A
    Dahmani, Y
    Ruiz-Pesini, E
    Montoya, J
    MEDICINA CLINICA, 2006, 126 (12): : 457 - 460
  • [32] A novel mitochondrial DNA point mutation in the tRNAIle gene:: Studies in a patient presenting with chronic progressive external ophthalmoplegia and multiple sclerosis
    Taylor, RW
    Chinnery, PF
    Bates, MJD
    Jackson, MJ
    Johnson, MA
    Andrews, RM
    Turnbull, DM
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 243 (01) : 47 - 51
  • [33] Mitochondrial DNA defects in Brazilian patients with chronic progressive external ophthalmoplegia
    Kiyomoto, BH
    Tengan, CH
    Moraes, CT
    Oliveira, ASB
    Gabbai, AA
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 1997, 152 (02) : 160 - 165
  • [34] A third locus predisposing to multiple deletions of mtDNA in autosomal dominant progressive external ophthalmoplegia
    Kaukonen, J
    Zeviani, M
    Comi, GP
    Piscaglia, MG
    Peltonen, L
    Suomalainen, A
    AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 65 (01) : 256 - 261
  • [35] MITOCHONDRIAL-DNA DELETIONS AND OPHTHALMOPLEGIA - REPLY
    MORAES, CT
    DIMAURO, S
    SHANSKE, S
    ROWLAND, LP
    NEW ENGLAND JOURNAL OF MEDICINE, 1990, 322 (10): : 701 - 701
  • [36] Multiple sclerosis and chronic progressive external ophthalmoplegia associated with a large scale mitochondrial DNA single deletion
    Gaetani, Lorenzo
    Mignarri, Andrea
    Di Gregorio, Maria
    Sarchielli, Paola
    Malandrini, Alessandro
    Cardaioli, Elena
    Calabresi, Paolo
    Dotti, Maria Teresa
    Di Filippo, Massimiliano
    JOURNAL OF NEUROLOGY, 2016, 263 (07) : 1449 - 1451
  • [37] Multiple sclerosis and chronic progressive external ophthalmoplegia associated with a large scale mitochondrial DNA single deletion
    Lorenzo Gaetani
    Andrea Mignarri
    Maria Di Gregorio
    Paola Sarchielli
    Alessandro Malandrini
    Elena Cardaioli
    Paolo Calabresi
    Maria Teresa Dotti
    Massimiliano Di Filippo
    Journal of Neurology, 2016, 263 : 1449 - 1451
  • [38] FUNCTIONAL RESPIRATORY-CHAIN STUDIES IN SUBJECTS WITH CHRONIC PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA AND LARGE HETEROPLASMIC MITOCHONDRIAL-DNA DELETIONS
    TROUNCE, I
    BYRNE, E
    MARZUKI, S
    DENNETT, X
    SUDOYO, H
    MASTAGLIA, F
    BERKOVIC, SF
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 1991, 102 (01) : 92 - 99
  • [39] Homozygous mutations in C1QBP as cause of progressive external ophthalmoplegia (PEO) and mitochondrial myopathy with multiple mtDNA deletions
    Marchet, Silvia
    Legati, Andrea
    Nasca, Alessia
    Di Meo, Ivano
    Spagnolo, Manuela
    Zanetti, Nadia
    Lamantea, Eleonora
    Catania, Alessia
    Lamperti, Costanza
    Ghezzi, Daniele
    HUMAN MUTATION, 2020, 41 (10) : 1745 - 1750
  • [40] Defects of intergenomic communication: Mutations of nuclear DNA and multiple deletions of mitochondrial DNA in chronic progressive external ophthalmologia
    Deschauer, M
    Zierz, S
    AKTUELLE NEUROLOGIE, 2003, 30 (03) : 103 - 106