Gannoun-Zaki L, Fournier-Bidoz S, Le Cam G, Chambon C, Millasseau P, Léger J J, Dechesne C A
INSERM Unité 300, Faculté de Pharmacie, Montpellier, France.
FEBS Lett. 1995 Nov 20;375(3):268-72. doi: 10.1016/0014-5793(95)01225-4.
In our search for genes up- or down-regulated genes in the mdx mouse model for Duchenne muscular dystrophy, we isolated a down-regulated mitochondrial DNA clone. In addition to this clone, all protein-coding mitochondrial genes tested had tissue-specific and age independent down-regulated expression. This implied mechanisms at the RNA level since no change in the mitochondrial DNA contents were detected. Cytochrome c oxidase activity showed the same range of down-regulated expression. These data provide a molecular basis for energetic metabolism modifications in mdx mice.
在我们对杜兴氏肌肉营养不良症的mdx小鼠模型中上调或下调基因的研究中,我们分离出了一个下调的线粒体DNA克隆。除了这个克隆外,所有检测的蛋白质编码线粒体基因都有组织特异性且与年龄无关的下调表达。由于未检测到线粒体DNA含量的变化,这暗示了RNA水平上的机制。细胞色素c氧化酶活性也呈现出相同程度的下调表达。这些数据为mdx小鼠能量代谢的改变提供了分子基础。