Farge Géraldine, Touraille Sylvie, Lachaume Philippe, Debise Roger, Procaccio Vincent, Alziari Serge
Equipe Génome Mitochondrial, UMR CNRS 6547, Université Blaise-Pascal, Clermont II, Aubière, France.
J Bioenerg Biomembr. 2004 Apr;36(2):203-10. doi: 10.1023/b:jobb.0000023624.06665.40.
We have studied a mutant strain of Drosophila in which 80% of the mitochondrial DNA molecules have lost over 30% of their coding region through deletion. This deletion affects genes encoding five subunits of complex I of the respiratory chain (NADH:ubiquinone oxidoreductase). The enzymatic activity of complex I in the mutant strain is half that in the wild strain, but ATP synthesis is unaffected. The drop in enzymatic activity of complex I in the mutant strain is associated with a 50% decrease in the quantity of constitutive proteins of the complex. Moreover, in the mutant strain there is a 50% decrease in the steady-state concentration of the transcripts of the mitochondrial genes affected by the deletion. This decrease is also observed for the transcripts of the nuclear genes coding for the subunits of complex I. These results suggest a coordination of the expression of the mitochondrial and nuclear genes coding for mitochondrial proteins.
我们研究了一种果蝇突变株,其中80%的线粒体DNA分子因缺失而失去了超过30%的编码区域。这种缺失影响了编码呼吸链复合体I(NADH:泛醌氧化还原酶)五个亚基的基因。突变株中复合体I的酶活性是野生株的一半,但ATP合成不受影响。突变株中复合体I酶活性的下降与该复合体组成蛋白数量减少50%有关。此外,在突变株中,受缺失影响的线粒体基因转录本的稳态浓度下降了50%。对于编码复合体I亚基的核基因转录本也观察到了这种下降。这些结果表明,编码线粒体蛋白的线粒体基因和核基因的表达存在协调。