Ferreirinha F, Duarte M, Melo A M, Videira A
Instituto de Biologia Molecular e Celular, Universidade do Porto, Rua do Campo Alegre 823, 4150 Porto, Portugal.
Biochem J. 1999 Sep 15;342 Pt 3(Pt 3):551-4.
We have cloned and inactivated in vivo, by repeat-induced point mutations, the nuclear gene encoding a 21 kDa subunit of complex I from Neurospora crassa. Mitochondria from the nuo21 mutant lack this specific protein but retain other subunits of complex I in approximately normal amounts. In addition, this mutant is able to assemble an almost intact enzyme. The electron transfer activities from NADH to artificial acceptors of mitochondrial membranes from nuo21 differ from those of the wild-type strain, suggesting that the absence of the 21 kDa polypeptide results in conformational changes in complex I. Nevertheless, complex I of nuo21 is able to perform NADH:ubiquinone reductase activity, as judged by the observation that the respiration of mutant mitochondria is sensitive to inhibition by rotenone. We discuss these findings in relation to the involvement of complex I in mitochondrial diseases.
我们通过重复诱导点突变在体内克隆并使编码粗糙脉孢菌复合体I 21 kDa亚基的核基因失活。来自nuo21突变体的线粒体缺乏这种特定蛋白质,但复合体I的其他亚基含量大致正常。此外,该突变体能够组装几乎完整的酶。nuo21线粒体膜从NADH到人工受体的电子传递活性与野生型菌株不同,这表明21 kDa多肽的缺失导致复合体I发生构象变化。然而,根据突变体线粒体呼吸对鱼藤酮抑制敏感这一观察结果判断,nuo21的复合体I能够进行NADH:泛醌还原酶活性。我们结合复合体I与线粒体疾病的关系讨论了这些发现。