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Relevant publications mentioning your query species (Homo sapiens):

  • Direct regulation of mitochondrial RNA synthesis by thyroid hormone.
    Enriquez JA, Fernandez-Silva P, Garrido-Perez N, Lopez-Perez MJ, Perez-Martos A, Montoya J
    Mol Cell Biol. 19(1):657-70 (1999).
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  • Abstract:
    We have analyzed the influence of in vivo treatment and in vitro addition of thyroid hormone on in organello mitochondrial DNA (mtDNA) transcription and, in parallel, on the in organello footprinting patterns at the mtDNA regions involved in the regulation of transcription. We found that thyroid hormone modulates mitochondrial RNA levels and the mRNA/rRNA ratio by influencing the transcriptional rate. In addition, we found conspicuous differences between the mtDNA dimethyl sulfate footprinting patterns of mitochondria derived from euthyroid and hypothyroid rats at the transcription initiation sites but not at the mitochondrial transcription termination factor (mTERF) binding region. Furthermore, direct addition of thyroid hormone to the incubation medium of mitochondria isolated from hypothyroid rats restored the mRNA/rRNA ratio found in euthyroid rats as well as the mtDNA footprinting patterns at the transcription initiation area. Therefore, we conclude that the regulatory effect of thyroid hormone on mitochondrial transcription is partially exerted by a direct influence of the hormone on the mitochondrial transcription machinery. Particularly, the influence on the mRNA/rRNA ratio is achieved by selective modulation of the alternative H-strand transcription initiation sites and does not require the previous activation of nuclear genes. These results provide the first functional demonstration that regulatory signals, such as thyroid hormone, that modify the expression of nuclear genes can also act as primary signals for the transcriptional apparatus of mitochondria.
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  • Structural and functional impairment of mitochondria in adriamycin-induced cardiomyopathy in mice: suppression of cytochrome c oxidase II (
    )
    gene expression.
    Papadopoulou LC, Theophilidis G, Thomopoulos GN, Tsiftsoglou AS
    Biochem Pharmacol. 57(5):481-9 (1999).
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  •  COXII, cytochrome c oxidase II 
     COXIII  ...
  • Nuclear-recessive mutations of factors involved in mitochondrial translation are responsible for age-related respiration deficiency of human skin fibroblasts.
    Isobe K, Ito S, Hosaka H, Iwamura Y, Kondo H, Kagawa Y, Hayashi JI
    J Biol Chem. 273(8):4601-6 (1998).
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  •  COII 
     COIII  ...
  • Asymmetrical directional mutation pressure in the mitochondrial genome of mammals.
    Reyes A, Gissi C, Pesole G, Saccone C
    Mol Biol Evol. 15(8):957-66 (1998).
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  •  COII 
     COIII  ...
  • Enhanced levels of several mitochondrial mRNA transcripts and mitochondrial superoxide production during ethinyl estradiol-induced hepatocarcinogenesis and after estrogen treatment of HepG2 cells.
    Chen J, Gokhale M, Li Y, Trush MA, Yager JD
    Carcinogenesis. 19(12):2187-93 (1998).
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  •  CO II, COII, Co II 
     CO III  ...
[truncated after 5 items ... view more]

Relevant publications mentioning other organisms:

  • Interactions of ribosome nascent chain complexes of the chloroplast-encoded D1 thylakoid membrane protein with cpSRP54.
    Nilsson R, Brunner J, Hoffman NE, van Wijk KJ
    EMBO J. 18(3):733-42 (1999).
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  •  Cox2p 
     Cox3p  ...
  • Direct regulation of mitochondrial RNA synthesis by thyroid hormone.
    Enriquez JA, Fernandez-Silva P, Garrido-Perez N, Lopez-Perez MJ, Perez-Martos A, Montoya J
    Mol Cell Biol. 19(1):657-70 (1999).
    Image not shown
  •  COII 
     COIII  ...
  • The deafness-associated mitochondrial DNA mutation at position 7445, which affects tRNASer(UCN) precursor processing, has long-range effects on NADH dehydrogenase subunit ND6 gene expression.
    Guan MX, Enriquez JA, Fischel-Ghodsian N, Puranam RS, Lin CP, Maw MA, Attardi G
    Mol Cell Biol. 18(10):5868-79 (1998).
    Image not shown
  •  COII 
     COIII  ...
  • The alloreactive T cell response against the class Ib molecule H2-M3 is specific for high affinity peptides.
    Dabhi VM, Hovik R, Van Kaer L, Lindahl KF
    J Immunol. 161(10):5171-8 (1998).
    Image not shown
  •  COII 
     COIII  ...
  • Nuclear-recessive mutations of factors involved in mitochondrial translation are responsible for age-related respiration deficiency of human skin fibroblasts.
    Isobe K, Ito S, Hosaka H, Iwamura Y, Kondo H, Kagawa Y, Hayashi JI
    J Biol Chem. 273(8):4601-6 (1998).
    Image not shown
  •  COII 
     COIII  ...
[truncated after 5 items ... view more]
[showing publications for 'MT-CO2' only]
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