Evidence that two reports of mtDNA cytochrome c oxidase "mutations" in Alzheimer's disease are based on nDNA pseudogenes of recent evolutionary origin

被引:29
作者
Davis, JN
Parker, WD
机构
[1] Univ Virginia, Ctr Hlth Sci, Dept Neurol, Charlottesville, VA 22903 USA
[2] Univ Virginia, Ctr Hlth Sci, Dept Neurosci, Charlottesville, VA 22903 USA
[3] Univ Virginia, Ctr Hlth Sci, Dept Pediat, Charlottesville, VA 22903 USA
[4] Univ Virginia, Ctr Hlth Sci, Ctr Study Neurodegenerat Dis, Charlottesville, VA 22903 USA
关键词
D O I
10.1006/bbrc.1998.8353
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Recently, two reports [R. E. Davis et al. (1997) Proc. Natl. Acad. Sci. USA 94, 4564-4569 and E. Fahy et al. (1997) Nucleic Acids Res. 25 3102-3109] described a series of heteroplasmic mitochondrial DNA (mtDNA) mutations in the genes encoding two cytochrome c oxidase subunits (CO1 and CO2) which segregated in higher abundance with Alzheimer's disease subjects than controls. Using mtDNA-depleted NT2 cells, we provide further evidence that these two reports are erroneously based on a PCR artifact arising from the amplification of nuclear DNA encoded mtDNA pseudogenes (mtDNA Psi s). Our findings are similar, but not identical, to other recent studies of these putative mtDNA Psi sequences. This sequence variability may indicate that multiple mtDNA Psi s, all of comparatively recent evolutionary origin are involved. While such pseudogenes are interesting in that they provide a molecular evolutionary "snapshot" of human ancestral mtDNA, it is unlikely that they play any role in the etiology of Alzheimer's disease. (C) 1998 Academic Press.
引用
收藏
页码:877 / 883
页数:7
相关论文
共 13 条
  • [1] SEQUENCE AND ORGANIZATION OF THE HUMAN MITOCHONDRIAL GENOME
    ANDERSON, S
    BANKIER, AT
    BARRELL, BG
    DEBRUIJN, MHL
    COULSON, AR
    DROUIN, J
    EPERON, IC
    NIERLICH, DP
    ROE, BA
    SANGER, F
    SCHREIER, PH
    SMITH, AJH
    STADEN, R
    YOUNG, IG
    [J]. NATURE, 1981, 290 (5806) : 457 - 465
  • [2] [Anonymous], 1989, SYNTHETIC OLIGONUCLE
  • [3] RAPID EVOLUTION OF ANIMAL MITOCHONDRIAL-DNA
    BROWN, WM
    GEORGE, M
    WILSON, AC
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1979, 76 (04) : 1967 - 1971
  • [4] INSERTIONS AND DUPLICATIONS OF MTDNA IN THE NUCLEAR GENOMES OF OLD-WORLD MONKEYS AND HOMINOIDS
    COLLURA, RV
    STEWART, CB
    [J]. NATURE, 1995, 378 (6556) : 485 - 489
  • [5] DAVIS RE, 1997, P NATL ACAD SCI USA, V94, P4564
  • [6] Multiplex fluorescence-based primer extension method for quantitative mutation analysis of mitochondrial DNA and its diagnostic application for Alzheimer's disease
    Fahy, E
    Nazarbaghi, R
    Zomorrodi, M
    Herrnstadt, C
    Parker, WD
    Davis, RE
    Ghosh, SS
    [J]. NUCLEIC ACIDS RESEARCH, 1997, 25 (15) : 3102 - 3109
  • [7] HILL A, 1988, YEARB PHYS ANTHROPOL, V31, P49
  • [8] Apparent mtDNA heteroplasmy in Alzheimer's disease patients and in normals due to PCR amplification of nucleus-embedded mtDNA pseudogenes
    Hirano, M
    Shtilbans, A
    Mayeux, R
    Davidson, MM
    DiMauro, S
    Knowles, JA
    Schon, EA
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (26) : 14894 - 14899
  • [9] 3 SEPARATE MITOCHONDRIAL-DNA SEQUENCES ARE CONTIGUOUS IN HUMAN GENOMIC DNA
    KAMIMURA, N
    ISHII, S
    MA, LD
    SHAY, JW
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1989, 210 (04) : 703 - 707
  • [10] RUVOLO M, 1993, MOL BIOL EVOL, V10, P1115