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Table 1.

Effect of in organello treatments on decay rates (k) and half-lives (t1/2) *of various mitochondrial genes using data from dot-blot analyses

ControlAnoxia+low pHAnoxiaAnoxia+1.5 mmol l−1 ATPLow pH
ATP6      
k 1.44×10−2 6.22×10−4 5.90×10−3 9.67×10−4 5.49×10−3 
t1/2 48.2 1113 117 716 187 
COX I      
k 6.75×10−3 9.58×10−4 1.90×10−3 3.65×10−3 5.49×10−3 
t1/2 102 723 364 194 126 
CYB      
k 1.03×10−2 1.37×10−3 NA 2.75×10−3 2.62×10−3 
t1/2 67.5 506 NA 252 264 
ND1      
k 1.48×10−2 NA 4.16×10−3 8.45×10−4 1.99×10−3 
t½ 47.0 NA 167 820 346 
ControlAnoxia+low pHAnoxiaAnoxia+1.5 mmol l−1 ATPLow pH
ATP6      
k 1.44×10−2 6.22×10−4 5.90×10−3 9.67×10−4 5.49×10−3 
t1/2 48.2 1113 117 716 187 
COX I      
k 6.75×10−3 9.58×10−4 1.90×10−3 3.65×10−3 5.49×10−3 
t1/2 102 723 364 194 126 
CYB      
k 1.03×10−2 1.37×10−3 NA 2.75×10−3 2.62×10−3 
t1/2 67.5 506 NA 252 264 
ND1      
k 1.48×10−2 NA 4.16×10−3 8.45×10−4 1.99×10−3 
t½ 47.0 NA 167 820 346 

ATP6, ATP synthase; COX1, cytochrome oxidase; CYB, cytochrome b;ND1, NADH dehydrogenase.

NA, increases in RNA amounts (although not statistically significant) make these assessments inapplicable.

*

Decay rates were calculated according to the formula for second-order decay kinetics: k=2.3/(time2-time1)×log(RNA1/RNA2). Half-life was calculated according to the equation t½=0.693/k(Segel, 1976).

k, min−1; t½, min.

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