A mutation in a mitochondrial dehydrogenase/reductase gene causes an increased sensitivity to oxidative stress and mitochondrial defects in the nematode Caenorhabditis elegans

被引:9
|
作者
Fujii, Michihiko [1 ]
Yasuda, Kayo [2 ,4 ]
Hartmann, Phil S. [3 ]
Ayusawa, Dai [1 ]
Ishii, Naoaki [2 ]
机构
[1] Yokohama City Univ, Grad Sch Nanobiosci, Kanazawa Ku, Yokohama, Kanagawa 2360027, Japan
[2] Tokai Univ, Sch Med, Dept Mol Life Sci, Kanagawa 2591193, Japan
[3] Texas Christian Univ, Dept Biol, Ft Worth, TX 76129 USA
[4] Tokai Univ, Educ & Res Support Ctr, Kanagawa 2591193, Japan
关键词
MDR SUPERFAMILY; MUTANT RAD-8; PROTEIN; OXYGEN; LONGEVITY; METABOLISM; EXPRESSION; RESISTANCE; DISORDERS; APOPTOSIS;
D O I
10.1111/j.1365-2443.2011.01547.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
rad-8 is an interesting mutant that shows increased sensitivities to UV radiation and reactive oxygen species in the nematode Caenorhabditis elegans. In this study, we have characterized rad-8 and have found that rad-8 showed several phenotypes of mitochondrial dysfunction such as a decreased activity of the respiratory chain, increased generation of superoxide anions, increased oxidative damage, increased apoptosis, and abnormal mitochondrial structure. Our genetic analysis has also indicated that rad-8 has a causative mutation in the F56H1.6 gene, which encodes a mitochondrial dehydrogenase/reductase. The functional role of RAD-8 may be evolutionarily conserved because expression of the putative human homologue RTIWIP/NIMP in rad-8 rescued the increased sensitivity to oxygen in rad-8. These results suggest that RAD-8 plays an important role in oxygen metabolism in mitochondria in higher eukaryotes.
引用
收藏
页码:1022 / 1034
页数:13
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