A unique junctional palindromic sequence in mitochondrial DNA from a patient with progressive external ophthalmoplegia

被引:6
|
作者
Saiwaki, T
Shiga, K
Fukuyama, R
Tsutsumi, Y
Fushiki, S
机构
[1] Kyoto Prefectural Univ Med, Dept Pathol & Appl Neurobiol, Res Inst Neurol Dis & Geriatr, Kamigyo Ku, Kyoto 6028566, Japan
[2] Kyoto Prefectural Univ Med, Dept Neurol & Gerontol, Res Inst Neurol Dis & Geriatr, Kyoto 602, Japan
来源
关键词
progressive external ophthalmoplegia; mitochondria; diagnosis; polymerase chain reaction;
D O I
10.1136/mp.53.6.333
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
A polymerase chain reaction (PCR) based procedure was modified to determine the deletion of mitochondrial DNA (mtDNA). The protocol consists of coamplification both of deleted and wild-type segments of mtDNA using a long PCR technique; evaluation of the deleted portion within the amplified DNA segments by restriction enzyme digestion followed by densitometrical analysis; and direct subcloning into a plasmid vector for DNA sequencing. The procedure revealed a 5.3 kb deletion of mtDNA in the biopsied muscle tissue obtained from a patient clinically diagnosed with progressive external ophthalmoplegia. The 5' and 3' sequences at both sides of the breakpoint comprise a 17 bp palindrome and 5 bp tandem repeats, suggesting that the deletion might occur through slipped mispairing and other novel mechanisms. This improved procedure has the potential to detect deletions occurring in the entire length of mtDNA, and mighty be useful for clinical screening of progressive external ophthalmoplegia.
引用
收藏
页码:333 / 335
页数:3
相关论文
共 50 条
  • [31] Large deletion (7.2 kb) of mitochondrial DNA with novel boundaries in a case of progressive external ophthalmoplegia
    Hirt, L
    Magistertti, PJ
    Hirt, L
    Bogousslavsky, J
    Boulat, O
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1996, 61 (04): : 422 - 423
  • [32] Chronic progressive external ophthalmoplegia with a novel mitochondrial DNA deletion and a mutation in the tRNALeu(UUR) gene
    Grünewald, T
    Porschke, H
    Goebel, H
    Reichmann, H
    Seibel, P
    DRUG DEVELOPMENT RESEARCH, 1999, 46 (01) : 80 - 85
  • [33] Mutations of mitochondrial DNA polymerase γA are a frequent cause of autosomal dominant or recessive progressive external ophthalmoplegia
    Lamantea, E
    Tiranti, V
    Bordoni, A
    Toscano, A
    Bono, F
    Servidei, S
    Papadimitriou, A
    Spelbrink, H
    Silvestri, L
    Casari, G
    Comi, GP
    Zeviani, M
    ANNALS OF NEUROLOGY, 2002, 52 (02) : 211 - 219
  • [34] Chronic progressive external ophthalmoplegia:: A new heteroplasmic tRNA Leu(CUN) mutation of mitochondrial DNA
    Cardaioli, E.
    Da Pozzo, P.
    Malfatti, E.
    Gallus, G. N.
    Rubegni, A.
    Malandrini, A.
    Gaudiano, C.
    Guidi, L.
    Serni, G.
    Berti, G.
    Dotti, M. T.
    Federico, A.
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2008, 272 (1-2) : 106 - 109
  • [35] Sporadic chronic progressive external ophthalmoplegia with single large mitochondrial DNA deletion and neurogenic findings
    Ruggiero, Lucia
    Fiorillo, Chiara
    Nesti, Claudia
    Manganelli, Fiore
    Iodice, Rosa
    Esposito, Marcello
    Santorelli, Filippo Maria
    Santoro, Lucio
    JOURNAL OF NEUROLOGY, 2017, 264 (03) : 597 - 599
  • [36] Sporadic chronic progressive external ophthalmoplegia with single large mitochondrial DNA deletion and neurogenic findings
    Lucia Ruggiero
    Chiara Fiorillo
    Claudia Nesti
    Fiore Manganelli
    Rosa Iodice
    Marcello Esposito
    Filippo Maria Santorelli
    Lucio Santoro
    Journal of Neurology, 2017, 264 : 597 - 599
  • [37] Parkinsonism and progressive external ophthalmoplegia with multiple mitochondrial DNA deletions: Report of two new cases
    Barton, B. R.
    Jackson, S.
    Diederich, N. J.
    MOVEMENT DISORDERS, 2010, 25 (07) : S494 - S494
  • [38] Parkinsonism and Progressive External Ophthalmoplegia with Multiple Mitochondrial DNA Deletions: Report of Two New Cases
    Barton, Brandon R.
    Jackson, Sandra
    Diederich, Nico
    NEUROLOGY, 2010, 74 (09) : A255 - A255
  • [39] MITOCHONDRIAL-DNA DELETIONS IN KEARNS-SAYRE SYNDROME AND IN MYOPATHIES WITH PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA
    NELSON, I
    DEGOUL, F
    MARSAC, C
    PONSOT, G
    LESTIENNE, P
    M S-MEDECINE SCIENCES, 1989, 5 (07): : 472 - 479
  • [40] Mitochondrial gene defect in patients with chronic progressive external ophthalmoplegia
    Chen, QT
    Li, XD
    Wu, LJ
    Qi, Y
    Wu, XR
    CHINESE MEDICAL JOURNAL, 1998, 111 (06) : 500 - 503