메뉴 건너뛰기




Volumn 314, Issue 4, 2004, Pages 1107-1112

Presence of interaction but not complementation between human mtDNAs carrying different mutations within a tRNALeu(UUR) gene

Author keywords

Complementation; Human; Mitochondrial DNA; Mitochondrial interaction

Indexed keywords

LEUCINE TRANSFER RNA; MITOCHONDRIAL DNA;

EID: 0942278963     PISSN: 0006291X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bbrc.2003.12.201     Document Type: Article
Times cited : (5)

References (16)
  • 2
    • 0031887129 scopus 로고    scopus 로고
    • Maternal inheritance of mouse mtDNA in interspecific hybrids: Segregation of the leaked paternal mtDNA followed by the prevention of subsequent paternal leakage
    • Shitara H., Hayashi J.-I., Takahama S., Kaneda H., Yonekawa H. Maternal inheritance of mouse mtDNA in interspecific hybrids: segregation of the leaked paternal mtDNA followed by the prevention of subsequent paternal leakage. Genetics. 148:1998;851-857.
    • (1998) Genetics , vol.148 , pp. 851-857
    • Shitara, H.1    Hayashi, J.-I.2    Takahama, S.3    Kaneda, H.4    Yonekawa, H.5
  • 3
    • 0028262917 scopus 로고
    • Human mitochondria and mitochondrial genome function as a single dynamic cellular unit
    • Hayashi J.-I., Takemitsu M., Goto Y., Nonaka I. Human mitochondria and mitochondrial genome function as a single dynamic cellular unit. J. Cell Biol. 125:1994;43-50.
    • (1994) J. Cell Biol. , vol.125 , pp. 43-50
    • Hayashi, J.-I.1    Takemitsu, M.2    Goto, Y.3    Nonaka, I.4
  • 4
    • 0025836655 scopus 로고
    • Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction
    • Hayashi J.-I., Ohta S., Kikuchi A., Takemitsu M., Goto Y., Nonaka I. Introduction of disease-related mitochondrial DNA deletions into HeLa cells lacking mitochondrial DNA results in mitochondrial dysfunction. Proc. Natl. Acad. Sci. USA. 88:1991;10614-10618.
    • (1991) Proc. Natl. Acad. Sci. USA , vol.88 , pp. 10614-10618
    • Hayashi, J.-I.1    Ohta, S.2    Kikuchi, A.3    Takemitsu, M.4    Goto, Y.5    Nonaka, I.6
  • 5
    • 0033772263 scopus 로고    scopus 로고
    • Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes
    • Inoue K., Nakada K., Ogura A., Isobe K., Goto Y., Nonaka I., Hayashi J.-I. Generation of mice with mitochondrial dysfunction by introducing mouse mtDNA carrying a deletion into zygotes. Nat. Genet. 26:2000;176-181.
    • (2000) Nat. Genet. , vol.26 , pp. 176-181
    • Inoue, K.1    Nakada, K.2    Ogura, A.3    Isobe, K.4    Goto, Y.5    Nonaka, I.6    Hayashi, J.-I.7
  • 6
    • 0034881326 scopus 로고    scopus 로고
    • Inter-mitochondrial complementation: Mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA
    • Nakada K., Inoue K., Ono T., Isobe K., Ogura A., Goto Y., Nonaka I., Hayashi J.-I. Inter-mitochondrial complementation: mitochondria-specific system preventing mice from expression of disease phenotypes by mutant mtDNA. Nat. Med. 7:2001;934-940.
    • (2001) Nat. Med. , vol.7 , pp. 934-940
    • Nakada, K.1    Inoue, K.2    Ono, T.3    Isobe, K.4    Ogura, A.5    Goto, Y.6    Nonaka, I.7    Hayashi, J.-I.8
  • 7
    • 0034938453 scopus 로고    scopus 로고
    • Human cells are protected from mitochondrial dysfunction by complementation of DNA products in fused mitochondria
    • Ono T., Isobe K., Nakada K., Hayashi J.-I. Human cells are protected from mitochondrial dysfunction by complementation of DNA products in fused mitochondria. Nat. Genet. 28:2001;272-275.
    • (2001) Nat. Genet. , vol.28 , pp. 272-275
    • Ono, T.1    Isobe, K.2    Nakada, K.3    Hayashi, J.-I.4
  • 8
    • 0026573082 scopus 로고
    • (Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes
    • (Leu(UUR)) mutation associated with mitochondrial myopathy, encephalopathy, lactic acidosis, and strokelike episodes. Mol. Cell. Biol. 12:1992;480-490.
    • (1992) Mol. Cell. Biol. , vol.12 , pp. 480-490
    • King, M.P.1    Koga, Y.2    Davidson, M.3    Schon, E.A.4
  • 9
    • 0026608057 scopus 로고
    • MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts
    • Chomyn A., Martinuzzi A., Yoneda M., Daga A., Hurko O., Johns D., Lai S.T., Nonaka I., Angelini C., Attardi G. MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts. Proc. Natl. Acad. Sci. USA. 89:1992;4221-4225.
    • (1992) Proc. Natl. Acad. Sci. USA , vol.89 , pp. 4221-4225
    • Chomyn, A.1    Martinuzzi, A.2    Yoneda, M.3    Daga, A.4    Hurko, O.5    Johns, D.6    Lai, S.T.7    Nonaka, I.8    Angelini, C.9    Attardi, G.10
  • 10
    • 0036544879 scopus 로고    scopus 로고
    • Inter-mitochondrial complementation of mtDNA mutations and nuclear context
    • Attardi G., Enriquez J.A., Cabezas-Herrera J. Inter-mitochondrial complementation of mtDNA mutations and nuclear context. Nat. Genet. 30:2002;360.
    • (2002) Nat. Genet. , vol.30 , pp. 360
    • Attardi, G.1    Enriquez, J.A.2    Cabezas-Herrera, J.3
  • 11
    • 0034646656 scopus 로고    scopus 로고
    • Very rare complementation between mitochondria carrying different mitochondrial DNA mutations points to intrinsic genetic autonomy of the organelles in cultured human cells
    • Enriquez J.A., Cabezas-Herrera J., Bayona-Bafaluy M.P., Attardi G. Very rare complementation between mitochondria carrying different mitochondrial DNA mutations points to intrinsic genetic autonomy of the organelles in cultured human cells. J. Biol. Chem. 275:2000;11207-11215.
    • (2000) J. Biol. Chem. , vol.275 , pp. 11207-11215
    • Enriquez, J.A.1    Cabezas-Herrera, J.2    Bayona-Bafaluy, M.P.3    Attardi, G.4
  • 12
    • 0012887965 scopus 로고    scopus 로고
    • Inter-mitochondrial complementation of mtDNA mutations and nuclear context
    • authors' reply 361
    • Hayashi J.-I., Nakada K., Ono T. Inter-mitochondrial complementation of mtDNA mutations and nuclear context. Nat. Genet. 30:2002;. authors' reply 361.
    • (2002) Nat. Genet. , vol.30
    • Hayashi, J.-I.1    Nakada, K.2    Ono, T.3
  • 13
    • 0036906665 scopus 로고    scopus 로고
    • Mitochondrial fusion in human cells is efficient, requires the inner membrane potential, and is mediated by mitofusins
    • Legros F., Lombes A., Frachon P., Rojo M. Mitochondrial fusion in human cells is efficient, requires the inner membrane potential, and is mediated by mitofusins. Mol. Biol. Cell. 13:2002;4343-4354.
    • (2002) Mol. Biol. Cell , vol.13 , pp. 4343-4354
    • Legros, F.1    Lombes, A.2    Frachon, P.3    Rojo, M.4
  • 14
    • 0037459089 scopus 로고    scopus 로고
    • Regulation of mitochondrial morphology by membrane potential, and DRP-dependent division and FZO1-dependent fusion reaction in mammalian cells
    • Ishihara N., Jofuku A., Eura Y., Mihara K. Regulation of mitochondrial morphology by membrane potential, and DRP-dependent division and FZO1-dependent fusion reaction in mammalian cells. Biochem. Biophys. Res. Commun. 301:2003;891-898.
    • (2003) Biochem. Biophys. Res. Commun. , vol.301 , pp. 891-898
    • Ishihara, N.1    Jofuku, A.2    Eura, Y.3    Mihara, K.4
  • 15
    • 0033515075 scopus 로고    scopus 로고
    • Functional integrity of mitochondrial genomes in human platelets and autopsied brain tissues from aged patients with Alzheimer's disease
    • Ito S., Inoue K., Yanagisawa N., Kaneko M., Hayashi J.-I. Functional integrity of mitochondrial genomes in human platelets and autopsied brain tissues from aged patients with Alzheimer's disease. Proc. Natl. Acad. Sci. USA. 96:1999;2099-2103.
    • (1999) Proc. Natl. Acad. Sci. USA , vol.96 , pp. 2099-2103
    • Ito, S.1    Inoue, K.2    Yanagisawa, N.3    Kaneko, M.4    Hayashi, J.-I.5
  • 16
    • 0024541837 scopus 로고
    • Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases
    • Linnane A.W., Marzuki S., Ozawa T., Tanaka M. Mitochondrial DNA mutations as an important contributor to ageing and degenerative diseases. Lancet. 1:1989;642-645.
    • (1989) Lancet , vol.1 , pp. 642-645
    • Linnane, A.W.1    Marzuki, S.2    Ozawa, T.3    Tanaka, M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.