scholarly journals Membrane topology of beef-heart ubiquinone-cytochrome c reductase (complex III).

1981 ◽  
Vol 256 (21) ◽  
pp. 11132-11136 ◽  
Author(s):  
H. Gutweniger ◽  
R. Bisson ◽  
C. Montecucco
1984 ◽  
Vol 217 (2) ◽  
pp. 551-560 ◽  
Author(s):  
R J Froud ◽  
C I Ragan

Ubiquinol oxidase has been reconstituted from ubiquinol-cytochrome c reductase (Complex III), cytochrome c and cytochrome c oxidase (Complex IV). The steady-state level of reduction of cytochrome c by ubiquinol-2 varies with the molar ratios of the complexes and with the presence of antimycin in a way that can be quantitatively accounted for by a model in which cytochrome c acts as a freely diffusible pool on the membrane. This model was based on that of Kröger & Klingenberg [(1973) Eur. J. Biochem. 34, 358-368] for ubiquinone-pool behaviour. Further confirmation of the pool model was provided by analysis of ubiquinol oxidase activity as a function of the molar ratio of the complexes and prediction of the degree of inhibition by antimycin.


2007 ◽  
Vol 85 (10) ◽  
pp. 986-996 ◽  
Author(s):  
Hung Huynh ◽  
Nicolas Servant ◽  
Lorraine E. Chalifour

Women and men do not respond identically to cardiac insults; premenopausal women are somewhat protected from cardiovascular disease. Our objective was to isolate and characterize hormone-responsive genes in the heart. Differential display identified an estrogen-inducible fragment that was found to encode the ubiquinol–cytochrome-c reductase (UCCR) 7.2 kDa protein of the mitochondrial respiratory complex III. We found UCCR7.2 mRNA to be highly expressed in the heart, and this expression increased in hearts of 4-, 10-, and 28-week-old spontaneously hypertensive rats (SHR) compared with normotensive Wistar–Kyoto rats. Oral hydralazine treatment to reduce hypertension reduced SHR UCCR7.2 expression. Cardiac UCCR7.2 mRNA expression was also increased significantly after a 5/6 nephrectomy compared with mock surgery. Cardiac expression after ovariectomy was 50% that of intact rats. Supplementation of ovariectomized rats with estrogen had no effect, whereas progesterone increased cardiac expression, although not to intact levels. No change in cardiac UCCR7.2 expression was found when intact rats were treated with either tamoxifen or ICI 182780. Thus, UCCR7.2 expression is reduced in the absence of ovarian hormones, but is not directly regulated by estrogen in the heart. We conclude that UCCR7.2 is a steroid hormone-responsive gene in the heart, with expression increased in cardiac hypertrophy and in response to hypertension.


1999 ◽  
Vol 104 (6) ◽  
pp. 460-466 ◽  
Author(s):  
Isabelle Valnot ◽  
Johanna Kassis ◽  
Dominique Chretien ◽  
Pascale de Lonlay ◽  
Béatrice Parfait ◽  
...  

Medicine ◽  
2020 ◽  
Vol 99 (44) ◽  
pp. e23026
Author(s):  
Xuncan Liu ◽  
Yanfeng Zhang ◽  
Jianmin Liang ◽  
Si Yang ◽  
Chen Chen

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