Effects QB disrupting the 21 kDa subunit of complex I from Neurospora crassa

被引:18
作者
Ferreirinha, F
Duarte, M
Melo, AMP
Videira, A
机构
[1] Univ Porto, Inst Biol Mol & Celular, P-4150 Porto, Portugal
[2] Univ Porto, Unidade Multidisciplinar Invest Biomed, P-4150 Porto, Portugal
[3] Univ Porto, Inst Ciencias Biomed Abel Salazar, P-4150 Porto, Portugal
关键词
complex I; gene disruption; mitochondria; mitochondrial diseases;
D O I
10.1042/0264-6021:3420551
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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 accepters of mitochondrial membranes from nuo21 differ from those of the wildtype 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.
引用
收藏
页码:551 / 554
页数:4
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