메뉴 건너뛰기




Volumn 85, Issue 1, 1999, Pages 20-30

Phylogenetic analysis of the mitochondrial genome indicates significant differences between patients with Alzheimer disease and controls in a French- Canadian founder population

Author keywords

Alzheimer disease; Founder population; Mitochondrial DNA sequence; Phylogenetic analysis

Indexed keywords

DNA; MITOCHONDRIAL DNA;

EID: 0033516529     PISSN: 01487299     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1096-8628(19990702)85:1<20::AID-AJMG6>3.0.CO;2-K     Document Type: Article
Times cited : (110)

References (44)
  • 3
    • 0028788493 scopus 로고
    • Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiples independent occurrences of the common mutations
    • Brown MD, Torroni A, Reckord CL, Wallace DC. 1995. Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiples independent occurrences of the common mutations. Hum Mutat 6:311-325.
    • (1995) Hum Mutat , vol.6 , pp. 311-325
    • Brown, M.D.1    Torroni, A.2    Reckord, C.L.3    Wallace, D.C.4
  • 4
    • 0026531040 scopus 로고
    • Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy
    • Brown MD, Voljavec AS, Lett MT, Torroni A, Yang CC, Wallace DC. 1992. Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy. Genetics 130:163-173.
    • (1992) Genetics , vol.130 , pp. 163-173
    • Brown, M.D.1    Voljavec, A.S.2    Lett, M.T.3    Torroni, A.4    Yang, C.C.5    Wallace, D.C.6
  • 5
    • 0021348482 scopus 로고
    • Polymorphic sites and the mechanism of evolution in human mitochondrial DNA
    • Cann RL, Brown WM, Wilson AC. 1984. Polymorphic sites and the mechanism of evolution in human mitochondrial DNA. Genetics 1106:479-499.
    • (1984) Genetics , vol.1106 , pp. 479-499
    • Cann, R.L.1    Brown, W.M.2    Wilson, A.C.3
  • 6
    • 0025322981 scopus 로고
    • Structure and function of cytochrome c oxidase
    • Capaldi RA. 1990. Structure and function of cytochrome c oxidase. Annu Rev Biochem 59:569-596.
    • (1990) Annu Rev Biochem , vol.59 , pp. 569-596
    • Capaldi, R.A.1
  • 7
    • 0028948660 scopus 로고
    • Distribution of brain cytochrome oxidase activity in various neurodegenerative diseases
    • Chagnon P, Bétard C, Robitaille Y, Cholette A, Gauvreau D. 1995. Distribution of brain cytochrome oxidase activity in various neurodegenerative diseases. Neuroreport 6:711-715.
    • (1995) Neuroreport , vol.6 , pp. 711-715
    • Chagnon, P.1    Bétard, C.2    Robitaille, Y.3    Cholette, A.4    Gauvreau, D.5
  • 8
    • 0030435646 scopus 로고    scopus 로고
    • Brain mitochondrial DNA polymorphism and cytochrome oxidase activity in Alzheimer disease
    • Chagnon P, Robitaille Y, Gauvreau D. 1996. Brain mitochondrial DNA polymorphism and cytochrome oxidase activity in Alzheimer disease. Alzheimer Research 2:237-242.
    • (1996) Alzheimer Research , vol.2 , pp. 237-242
    • Chagnon, P.1    Robitaille, Y.2    Gauvreau, D.3
  • 9
    • 0030016323 scopus 로고    scopus 로고
    • Increased risk of dementia in mothers of Alzheimer's disease cases: Evidence for maternal inheritance
    • Edland SD, Silvermann JM, Peskind ER, Tsuang D, Wijsman E, Morris JC. 1996. Increased risk of dementia in mothers of Alzheimer's disease cases: Evidence for maternal inheritance. Neurology 47:254-256.
    • (1996) Neurology , vol.47 , pp. 254-256
    • Edland, S.D.1    Silvermann, J.M.2    Peskind, E.R.3    Tsuang, D.4    Wijsman, E.5    Morris, J.C.6
  • 11
    • 0023191278 scopus 로고
    • Intercorrelations of regional cerebral glucose metabolic rates in Alzheimer's disease
    • Horwitz B, Grady CL, Schlageter NL, Duara R, Rapoport SI. 1987. Intercorrelations of regional cerebral glucose metabolic rates in Alzheimer's disease. Brain Res 407:294-306.
    • (1987) Brain Res , vol.407 , pp. 294-306
    • Horwitz, B.1    Grady, C.L.2    Schlageter, N.L.3    Duara, R.4    Rapoport, S.I.5
  • 13
    • 0026408618 scopus 로고
    • Abnormalities of glucose metabolism in Alzheimer's disease
    • Hoyer S. 1991. Abnormalities of glucose metabolism in Alzheimer's disease. Ann NY Acad Sci 640:53-58.
    • (1991) Ann NY Acad Sci , vol.640 , pp. 53-58
    • Hoyer, S.1
  • 14
    • 0023737618 scopus 로고
    • Glucose metabolism as the site of the primary abnormality in early-onset dementia of Alzheimer type
    • Hoyer S, Oesterreich K, Wagner O. 1988. Glucose metabolism as the site of the primary abnormality in early-onset dementia of Alzheimer type. J Neurol 235:143-148.
    • (1988) J Neurol , vol.235 , pp. 143-148
    • Hoyer, S.1    Oesterreich, K.2    Wagner, O.3
  • 15
    • 0029091194 scopus 로고
    • A mitochondrial DNA clone is associated with increased risk for Alzheimer disease
    • Hutchin T, Cortopassi G. 1995. A mitochondrial DNA clone is associated with increased risk for Alzheimer disease. Proc Natl Acad Sci USA 92:6892-6895.
    • (1995) Proc Natl Acad Sci USA , vol.92 , pp. 6892-6895
    • Hutchin, T.1    Cortopassi, G.2
  • 16
    • 0026337654 scopus 로고
    • Cytochrome b mutations in Leber hereditary optic neuropathy
    • Johns DR, Neufeld MJ. 1991. Cytochrome b mutations in Leber hereditary optic neuropathy. Biochem Biophys Res Commun 181:1358-1364.
    • (1991) Biochem Biophys Res Commun , vol.181 , pp. 1358-1364
    • Johns, D.R.1    Neufeld, M.J.2
  • 17
    • 0022414054 scopus 로고
    • Diagnosis of Alzheimer's disease
    • Khachaturian ZS. 1985. Diagnosis of Alzheimer's disease. Arch Neurol 59:1097-1105.
    • (1985) Arch Neurol , vol.59 , pp. 1097-1105
    • Khachaturian, Z.S.1
  • 19
    • 0027935035 scopus 로고
    • No association of mutations at nucleotide 5460 of mitochondrial NADH dehydrogenase with Alzheimer's disease
    • Kösel S, Egensperger R, Mehraein P, Graeber MB. 1994. No association of mutations at nucleotide 5460 of mitochondrial NADH dehydrogenase with Alzheimer's disease. Biochem Biophys Res Commun 203:745-749.
    • (1994) Biochem Biophys Res Commun , vol.203 , pp. 745-749
    • Kösel, S.1    Egensperger, R.2    Mehraein, P.3    Graeber, M.B.4
  • 23
    • 0021271971 scopus 로고
    • Clinical diagnosis of Alzheimer's disease: Report of the NINCDSADRDA work group under the auspices of department of health and human services task force on Alzheimer's disease
    • McKhann G, Drachman D, Folstein M, Katzman R, Price D, Stadlan EM. 1984. Clinical diagnosis of Alzheimer's disease: report of the NINCDSADRDA work group under the auspices of department of health and human services task force on Alzheimer's disease. Neurology 34:939-944.
    • (1984) Neurology , vol.34 , pp. 939-944
    • McKhann, G.1    Drachman, D.2    Folstein, M.3    Katzman, R.4    Price, D.5    Stadlan, E.M.6
  • 24
    • 0028152717 scopus 로고
    • Oxidative damage to mitochondrial DNA is increased in Alzheimer's disease
    • Mecocci P, MacGarvey U, Beal F. 1994. Oxidative damage to mitochondrial DNA is increased in Alzheimer's disease. Ann Neurol 36:747-751.
    • (1994) Ann Neurol , vol.36 , pp. 747-751
    • Mecocci, P.1    MacGarvey, U.2    Beal, F.3
  • 25
    • 0345363736 scopus 로고
    • Center for Molecular Medicine Emory University, Atlanta, GA
    • MITOMAP. 1995. Human Mitochondrial Genome Database. Center for Molecular Medicine Emory University, Atlanta, GA. http.//www.gen.emory.edu/mitomap.html.
    • (1995) Human Mitochondrial Genome Database
  • 26
    • 0027145131 scopus 로고
    • Two novel pathogenic mitochondrial DNA mutation affecting organelle number and protein synthesis: Is tRNALeu(UUR) gene an etiologic hot spot
    • Moraes CT, Ciacci F, Bonilla E, Jansen C, Hirano M, Rao N, Lovelace LP, Schon EA, DiMauro S. 1993. Two novel pathogenic mitochondrial DNA mutation affecting organelle number and protein synthesis: is tRNALeu(UUR) gene an etiologic hot spot. J Clin Invest 92:2906-2915.
    • (1993) J Clin Invest , vol.92 , pp. 2906-2915
    • Moraes, C.T.1    Ciacci, F.2    Bonilla, E.3    Jansen, C.4    Hirano, M.5    Rao, N.6    Lovelace, L.P.7    Schon, E.A.8    DiMauro, S.9
  • 27
    • 0025024024 scopus 로고
    • Cytochrome oxidase deficiency in Alzheimer's disease
    • Parker WD, Filley CM, Parks JK. 1990. Cytochrome oxidase deficiency in Alzheimer's disease. Neurology 40:1302-1303.
    • (1990) Neurology , vol.40 , pp. 1302-1303
    • Parker, W.D.1    Filley, C.M.2    Parks, J.K.3
  • 28
    • 0029055772 scopus 로고
    • Cytochrome c oxidase in Alzheimer's disease brain: Purification and characterization
    • Parker WD, Parks JK. 1995. Cytochrome c oxidase in Alzheimer's disease brain: Purification and characterization. Neurology 45:482-486.
    • (1995) Neurology , vol.45 , pp. 482-486
    • Parker, W.D.1    Parks, J.K.2
  • 30
    • 0343050763 scopus 로고
    • Alterations in calcium content and biochemical processes in cultured skin fibroblasts from aged and Alzheimer donors
    • Peterson C, Goldman JE. 1986. Alterations in calcium content and biochemical processes in cultured skin fibroblasts from aged and Alzheimer donors. Proc Natl Acad Sci USA 83:2758-2762.
    • (1986) Proc Natl Acad Sci USA , vol.83 , pp. 2758-2762
    • Peterson, C.1    Goldman, J.E.2
  • 31
    • 0026672905 scopus 로고
    • Is a point mutation in the mitochondrial ND2 gene associated with Alzheimer's disease
    • Petruzzella V, Chen X, Schon EA. 1992. Is a point mutation in the mitochondrial ND2 gene associated with Alzheimer's disease. Biochem Biophys Res Commun 186:491-497.
    • (1992) Biochem Biophys Res Commun , vol.186 , pp. 491-497
    • Petruzzella, V.1    Chen, X.2    Schon, E.A.3
  • 32
    • 0025914324 scopus 로고
    • Abnormal brain glucose metabolism in Alzheimer's disease as measured by position emission tomography
    • Rapoport SI, Horwitz B, Grady CL, Haxby JV, DeCarli C, Schapiro MB. 1991. Abnormal brain glucose metabolism in Alzheimer's disease as measured by position emission tomography. Adv Exp Med Biol 291: 231-248.
    • (1991) Adv Exp Med Biol , vol.291 , pp. 231-248
    • Rapoport, S.I.1    Horwitz, B.2    Grady, C.L.3    Haxby, J.V.4    DeCarli, C.5    Schapiro, M.B.6
  • 36
    • 0031985058 scopus 로고    scopus 로고
    • Exhaustive scanning approach to screen all the mitochondrial tRNA genes for mutations and its application to the investigation of 35 independent patients with mitochondrial disorders
    • Sternberg D, Danan C, Lombes A, Laforet P, Girodon E, Goossens M, Amselem S. 1998. Exhaustive scanning approach to screen all the mitochondrial tRNA genes for mutations and its application to the investigation of 35 independent patients with mitochondrial disorders. Hum Mol Genet 7:33-42..
    • (1998) Hum Mol Genet , vol.7 , pp. 33-42
    • Sternberg, D.1    Danan, C.2    Lombes, A.3    Laforet, P.4    Girodon, E.5    Goossens, M.6    Amselem, S.7
  • 38
    • 0030879372 scopus 로고    scopus 로고
    • Mitochondrial DNA and disease
    • Suomalainen A. 1997. Mitochondrial DNA and disease. Ann Med 29:235-246.
    • (1997) Ann Med , vol.29 , pp. 235-246
    • Suomalainen, A.1
  • 39
    • 0343636775 scopus 로고
    • Retrospective assessment of relative risks of coronary arteriosclerosis and myocardial infarct in autopsy confirmed dementias of the AD and non-AD types
    • New York: John Wiley & Sons Ltd
    • Tiberghien D, Robitaille Y, Laroche-Cholette A, Houde L, Grenon M, Gauvreau D. 1993. Retrospective assessment of relative risks of coronary arteriosclerosis and myocardial infarct in autopsy confirmed dementias of the AD and non-AD types. In Alzheimer's Disease: Advances in Clinical and Basic Research. New York: John Wiley & Sons Ltd, 121-127.
    • (1993) Alzheimer's Disease: Advances in Clinical and Basic Research , pp. 121-127
    • Tiberghien, D.1    Robitaille, Y.2    Laroche-Cholette, A.3    Houde, L.4    Grenon, M.5    Gauvreau, D.6
  • 40
    • 16944363113 scopus 로고    scopus 로고
    • Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484
    • Torroni A, Petrozzi M, D'Urbano L, Sellitto D, Zeviani M, Carrara F, Carducci C, Leuzzi V, Carelli V, Barboni P, De Negri A, Scozzari R. 1997. Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484. Am J Hum Genet 60:1107-1121.
    • (1997) Am J Hum Genet , vol.60 , pp. 1107-1121
    • Torroni, A.1    Petrozzi, M.2    D'Urbano, L.3    Sellitto, D.4    Zeviani, M.5    Carrara, F.6    Carducci, C.7    Leuzzi, V.8    Carelli, V.9    Barboni, P.10    De Negri, A.11    Scozzari, R.12
  • 41
    • 0028233947 scopus 로고
    • Mitochondrial DNA mutations in diseases of energy metabolism
    • Wallace DC. 1994. Mitochondrial DNA mutations in diseases of energy metabolism. J Bioenerg Biomembr 26:241-250.
    • (1994) J Bioenerg Biomembr , vol.26 , pp. 241-250
    • Wallace, D.C.1
  • 43
    • 0024561501 scopus 로고
    • Cytochrome oxidase: An endogenous metabolic marker for neuronal activity
    • Wong-Riley MTT. 1989. Cytochrome oxidase: an endogenous metabolic marker for neuronal activity. Trends Neurosci 12:94-101.
    • (1989) Trends Neurosci , vol.12 , pp. 94-101
    • Wong-Riley, M.T.T.1
  • 44
    • 0028843809 scopus 로고
    • No association found between Alzheimer's disease and a mitochondrial tRNA glutamine gene variant
    • Wragg MA, Talbot CJ, Morris JC, Lendon CL, Goate AM. 1995. No association found between Alzheimer's disease and a mitochondrial tRNA glutamine gene variant. Neurosci Lett 201:107-110.
    • (1995) Neurosci Lett , vol.201 , pp. 107-110
    • Wragg, M.A.1    Talbot, C.J.2    Morris, J.C.3    Lendon, C.L.4    Goate, A.M.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.