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Volumn 47, Issue 5, 2006, Pages 1810-1816

Differential mitochondrial DNA and gene expression in inherited retinal dysplasia in miniature Schnauzer dogs

Author keywords

[No Author keywords available]

Indexed keywords

COMPLEMENTARY DNA; CYTOCHROME C OXIDASE; GLYCERALDEHYDE 3 PHOSPHATE DEHYDROGENASE; MESSENGER RNA; MITOCHONDRIAL DNA; REDUCED NICOTINAMIDE ADENINE DINUCLEOTIDE DEHYDROGENASE; GLYCERALDEHYDE 3 PHOSPHATE DEHYDROGENASE (NADP); RNA;

EID: 33744766773     PISSN: 01460404     EISSN: None     Source Type: Journal    
DOI: 10.1167/iovs.05-0819     Document Type: Article
Times cited : (15)

References (32)
  • 3
    • 2342488125 scopus 로고    scopus 로고
    • Inherited retinal dysplasia in Miniature Schnauzer dogs
    • Grahn BH, Storey ES, McMillan C. Inherited retinal dysplasia in Miniature Schnauzer dogs. Vet Ophthalmol. 2004;7:151-158.
    • (2004) Vet Ophthalmol , vol.7 , pp. 151-158
    • Grahn, B.H.1    Storey, E.S.2    McMillan, C.3
  • 5
    • 0017364477 scopus 로고
    • Experimental retinal dysplasia due to cytosine arabinoside
    • Percy DH, Danylchuk KD. Experimental retinal dysplasia due to cytosine arabinoside. Invest Ophthalmol Vis Sci. 1977;16:353-364.
    • (1977) Invest Ophthalmol Vis Sci , vol.16 , pp. 353-364
    • Percy, D.H.1    Danylchuk, K.D.2
  • 7
    • 0040165888 scopus 로고
    • Heredity of retinal dysplasia in Bedlington Terriers
    • Rubin LF. Heredity of retinal dysplasia in Bedlington Terriers. J Am Vet Med Assoc. 1968;152:260-262.
    • (1968) J Am Vet Med Assoc , vol.152 , pp. 260-262
    • Rubin, L.F.1
  • 8
    • 0017887568 scopus 로고
    • Heritability of multifocal retinal dysplasia
    • MacMillan AD, Lipton DE. Heritability of multifocal retinal dysplasia. J Am Vet Med Assoc. 1978;172:568-572.
    • (1978) J Am Vet Med Assoc , vol.172 , pp. 568-572
    • MacMillan, A.D.1    Lipton, D.E.2
  • 10
    • 0024289345 scopus 로고
    • Inheritance of associated ocular and skeletal dysplasia in Labrador Retrievers
    • Carrig CB, Sponenberg DP, Schmidt GM, Tvedten HW. Inheritance of associated ocular and skeletal dysplasia in Labrador Retrievers. J Am Vet Med Assoc. 1988;193:1269-1272.
    • (1988) J Am Vet Med Assoc , vol.193 , pp. 1269-1272
    • Carrig, C.B.1    Sponenberg, D.P.2    Schmidt, G.M.3    Tvedten, H.W.4
  • 11
    • 0020531422 scopus 로고    scopus 로고
    • O Toole D, Young S, Severin GA, Neumann S. Retinal dysplasia in English Springer Spaniel dogs: light microscopy of the post-natal lesions. Vet Pathol. 1983;20:298-311.
    • O Toole D, Young S, Severin GA, Neumann S. Retinal dysplasia in English Springer Spaniel dogs: light microscopy of the post-natal lesions. Vet Pathol. 1983;20:298-311.
  • 12
    • 0025809513 scopus 로고
    • Dysplastic canine retinal morphogenesis
    • Whitely HL. Dysplastic canine retinal morphogenesis. Invest Ophthalmol Vis Sci. 1991;32:1492-1498.
    • (1991) Invest Ophthalmol Vis Sci , vol.32 , pp. 1492-1498
    • Whitely, H.L.1
  • 13
    • 0028359658 scopus 로고
    • Direct isolation of polymorphic markers linked to a trait by genetically directed representational difference analysis
    • Lisitsyn NA, Segre JA, Kusumi K, et al. Direct isolation of polymorphic markers linked to a trait by genetically directed representational difference analysis. Nat Genet. 1994;6:57-63.
    • (1994) Nat Genet , vol.6 , pp. 57-63
    • Lisitsyn, N.A.1    Segre, J.A.2    Kusumi, K.3
  • 14
    • 0347928918 scopus 로고    scopus 로고
    • Cloning and characterization of the canine photoreceptor specific cone-rod homeobox (CRX) gene and evaluation as a candidate for early onset photoreceptor diseases in the dog
    • Akhmedov NB, Baldwin VJ, Zangerl B, et al. Cloning and characterization of the canine photoreceptor specific cone-rod homeobox (CRX) gene and evaluation as a candidate for early onset photoreceptor diseases in the dog. Mol Vis. 2002;8:79-84.
    • (2002) Mol Vis , vol.8 , pp. 79-84
    • Akhmedov, N.B.1    Baldwin, V.J.2    Zangerl, B.3
  • 15
    • 0033860249 scopus 로고    scopus 로고
    • Isolation of DNA markers informative in purebred dog families by genomic representational difference analysis (gRDA)
    • Everts RE, Versteeg SA, Renier C, et al. Isolation of DNA markers informative in purebred dog families by genomic representational difference analysis (gRDA). Mamm Genome. 2000;11:741-747.
    • (2000) Mamm Genome , vol.11 , pp. 741-747
    • Everts, R.E.1    Versteeg, S.A.2    Renier, C.3
  • 16
    • 4444256134 scopus 로고    scopus 로고
    • Differences in expression of retinal pigment epithelium mRNA between normal canines
    • Hanik HJ, Loewen ME, Appleyard GD, Grahn BH, Forsyth GW. Differences in expression of retinal pigment epithelium mRNA between normal canines. Can J Vet Res. 2004;68:201-207.
    • (2004) Can J Vet Res , vol.68 , pp. 201-207
    • Hanik, H.J.1    Loewen, M.E.2    Appleyard, G.D.3    Grahn, B.H.4    Forsyth, G.W.5
  • 17
    • 0028577898 scopus 로고
    • Identifying differences in mRNA expression by representational difference analysis of cDNA
    • Hubank M, Schatz DG. Identifying differences in mRNA expression by representational difference analysis of cDNA. Nucleic Acids Res. 1994;22:5640-5648.
    • (1994) Nucleic Acids Res , vol.22 , pp. 5640-5648
    • Hubank, M.1    Schatz, D.G.2
  • 18
    • 17344392308 scopus 로고    scopus 로고
    • A new mathematical model for relative quantification in real-time RT-PCR
    • Pfaffl MW. A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res. 2001;29:2002-2007.
    • (2001) Nucleic Acids Res , vol.29 , pp. 2002-2007
    • Pfaffl, M.W.1
  • 19
    • 11344277076 scopus 로고    scopus 로고
    • Transient over-expression of mitochondrial transcription factor A (TFAM) is sufficient to stimulate mitochondrial DNA transcription, but not sufficient to increase mitochondrial DNA copy number
    • Maniura-Weber K, Goffart S, Garstka HL, Montoya J, Wiesner RJ. Transient over-expression of mitochondrial transcription factor A (TFAM) is sufficient to stimulate mitochondrial DNA transcription, but not sufficient to increase mitochondrial DNA copy number. Nucleic Acids Res. 2004;32:6015-6027.
    • (2004) Nucleic Acids Res , vol.32 , pp. 6015-6027
    • Maniura-Weber, K.1    Goffart, S.2    Garstka, H.L.3    Montoya, J.4    Wiesner, R.J.5
  • 20
    • 14644414173 scopus 로고    scopus 로고
    • Mitochondrial DNA 3243A→G mutation and increased expression of LARS2 gene in the brains of patients with bipolar disorder and schizophrenia
    • Munakata K, Iwamoto K, Bundo M, Kato T. Mitochondrial DNA 3243A→G mutation and increased expression of LARS2 gene in the brains of patients with bipolar disorder and schizophrenia. Biol Psychiatry. 2005;57:525-532.
    • (2005) Biol Psychiatry , vol.57 , pp. 525-532
    • Munakata, K.1    Iwamoto, K.2    Bundo, M.3    Kato, T.4
  • 21
    • 1942453308 scopus 로고    scopus 로고
    • The mtDNA T8993G (NARP) mutation results in an impairment of oxidative phosphorylation that can be improved by antioxidants
    • Mattiazzi M, Vijayvergiya C, Gajewski CD, et al. The mtDNA T8993G (NARP) mutation results in an impairment of oxidative phosphorylation that can be improved by antioxidants. Hum Mol Genet. 2004;13:869-879.
    • (2004) Hum Mol Genet , vol.13 , pp. 869-879
    • Mattiazzi, M.1    Vijayvergiya, C.2    Gajewski, C.D.3
  • 22
    • 0028949749 scopus 로고
    • The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation
    • Riordan-Eva P, Sanders MD, Govan GG, Sweeney MG, Da Costa J, Harding AE. The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation. Brain. 1995;118:319-337.
    • (1995) Brain , vol.118 , pp. 319-337
    • Riordan-Eva, P.1    Sanders, M.D.2    Govan, G.G.3    Sweeney, M.G.4    Da Costa, J.5    Harding, A.E.6
  • 23
    • 0032176078 scopus 로고    scopus 로고
    • The complete nucleotide sequence of the domestic dog (Canis familiaris) mitochondrial genome
    • Kim KS, Lee SE, Jeong HW, Ha JH. The complete nucleotide sequence of the domestic dog (Canis familiaris) mitochondrial genome. Mol Phylogenet Evol. 1998;10:210-220.
    • (1998) Mol Phylogenet Evol , vol.10 , pp. 210-220
    • Kim, K.S.1    Lee, S.E.2    Jeong, H.W.3    Ha, J.H.4
  • 24
    • 2442431673 scopus 로고    scopus 로고
    • Mitochondrial transcription factor A regulates mtDNA copy number in mammals
    • Ekstrand MI, Falkenberg M, Rantanen A, et al. Mitochondrial transcription factor A regulates mtDNA copy number in mammals. Hum Mol Genet. 2004;13:935-944.
    • (2004) Hum Mol Genet , vol.13 , pp. 935-944
    • Ekstrand, M.I.1    Falkenberg, M.2    Rantanen, A.3
  • 25
    • 0141634243 scopus 로고    scopus 로고
    • Depressed mitochondrial transcription factors and oxidative capacity in rat failing cardiac and skeletal muscles
    • Garnier A, Fortin C, Delomenie C, Momken I, Veksler V, Ventura-Clapier R. Depressed mitochondrial transcription factors and oxidative capacity in rat failing cardiac and skeletal muscles. J Physiol. 2003;551:491-501.
    • (2003) J Physiol , vol.551 , pp. 491-501
    • Garnier, A.1    Fortin, C.2    Delomenie, C.3    Momken, I.4    Veksler, V.5    Ventura-Clapier, R.6
  • 26
    • 0028029271 scopus 로고
    • Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletion
    • Poulton J, Morten K, Freeman-Emmerson C, et al. Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletion. Hum Mol Genett. 1994;3:1763-1769.
    • (1994) Hum Mol Genett , vol.3 , pp. 1763-1769
    • Poulton, J.1    Morten, K.2    Freeman-Emmerson, C.3
  • 27
    • 0034575038 scopus 로고    scopus 로고
    • Abnormal levels of human mitochondrial transcription factor A in skeletal muscle in mitochondrial encephalomyopathies
    • Siciliano G, Mancuso M, Pasquali L, Manca ML, Tessa A, Iudice A. Abnormal levels of human mitochondrial transcription factor A in skeletal muscle in mitochondrial encephalomyopathies. Neurol Sci. 2000;21(suppl 5):S985-S987.
    • (2000) Neurol Sci , vol.21 , Issue.SUPPL. 5
    • Siciliano, G.1    Mancuso, M.2    Pasquali, L.3    Manca, M.L.4    Tessa, A.5    Iudice, A.6
  • 28
    • 0036389569 scopus 로고    scopus 로고
    • Human mitochondrial transcription factor A reduction and mitochondrial dysfunction in Hashimoto's hypothyroid myopathy
    • Siciliano G, Monzani F, Manca ML, et al. Human mitochondrial transcription factor A reduction and mitochondrial dysfunction in Hashimoto's hypothyroid myopathy. Mol Med. 2002;8:326-333.
    • (2002) Mol Med , vol.8 , pp. 326-333
    • Siciliano, G.1    Monzani, F.2    Manca, M.L.3
  • 29
    • 0034724327 scopus 로고    scopus 로고
    • Genetic modification of survival in tissue-specific knockout mice with mitochondrial cardiomyopathy
    • Li H, Wang J, Wilhelmsson H, et al. Genetic modification of survival in tissue-specific knockout mice with mitochondrial cardiomyopathy. Proc Natl Acad Sci USA. 2000;97:3467-3472.
    • (2000) Proc Natl Acad Sci USA , vol.97 , pp. 3467-3472
    • Li, H.1    Wang, J.2    Wilhelmsson, H.3
  • 30
    • 0042632864 scopus 로고    scopus 로고
    • Human mitochondrial transcription factor B1 interacts with the C-terminal activation region of h-mtTFA and stimulates transcription independently of its RNA methyltransferase activity
    • McCulloch V, Shadel GS. Human mitochondrial transcription factor B1 interacts with the C-terminal activation region of h-mtTFA and stimulates transcription independently of its RNA methyltransferase activity. Mol Cell Biol. 2003;16:5816-5824.
    • (2003) Mol Cell Biol , vol.16 , pp. 5816-5824
    • McCulloch, V.1    Shadel, G.S.2
  • 32
    • 0034326946 scopus 로고    scopus 로고
    • Mitochondrial genetics and disease
    • Schon EA. Mitochondrial genetics and disease. Trends Biochem Sci. 2000;25:555-560.
    • (2000) Trends Biochem Sci , vol.25 , pp. 555-560
    • Schon, E.A.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.