Different respiratory defective phenotypes of Neurospora crassa and Saccharomyces cerevisiae after inactivation of the gene encoding the mitochondrial acyl carrier protein

被引:92
作者
Schneider, R [1 ]
Massow, M [1 ]
Lisowsky, T [1 ]
Weiss, H [1 ]
机构
[1] UNIV DUSSELDORF,INST BOT,D-40225 DUSSELDORF,GERMANY
关键词
acyl carrier protein; NADH; ubiquinone oxidoreductase; PET gene; fatty acid synthesis;
D O I
10.1007/BF00313188
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The nuclear genes (ncp-1, ACP1) encoding the mitochondrial acyl carrier protein were disrupted in Meurospora crassa and Saccharomyces cerevisiae. In N. crassa acp-1 is a peripheral subunit of the respiratory NADH:ubiquinone oxidoreductase (complex I). S. cerevisiae lacks complex I and its ACP1 appears to be located in the mitochondrial matrix. The loss of acp-1 in N. crassa causes two biochemical lesions. Firstly, the peripheral part of complex I is not assembled, and the membrane part is not properly assembled. The respiratory ubiquinol: cytochrome c oxidoreductase (complex III) and cytochrome c oxidase (complex IV) are normal amounts. Secondly, the lysophospholipid of mitochondrial membranes is increased four-fold. In S. cerevisiae, the loss of ACP1 leads to a pleiotropic respiratory deficient phenotype.
引用
收藏
页码:10 / 17
页数:8
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