Zhu D, Scandalios J G
Department of Genetics, North Carolina State University, Raliegh 27695, USA.
Free Radic Biol Med. 1995 Feb;18(2):179-83. doi: 10.1016/0891-5849(94)00113-x.
We recently demonstrated that maize mitochondrial MnSODs are encoded by a differentially expressed multigene family. Molecular characterization of the cloned maize MnSod cDNAs shows that all the maize MnSODs encoded by the cloned MnSod have mitochondrial transit peptides and that the matrix-targeting signal was conserved in all the MnSOD precursor proteins, suggesting that all the maize MnSODs are associated with mitochondria in vivo. In an attempt to clarify the submitochondrial localization of each individual maize MnSOD, each of the maize MnSod cDNAs was introduced into the MnSOD-deficient yeast cells. The functional role and submitochondrial location of each individual MnSOD were examined in the transformed yeast cells. Herein, we demonstrate that all the maize MnSODs can functionally complement the MnSOD deficiency and rescue the transformed yeast cells from oxidative stress induced by paraquat. Biochemical analyses indicate that all of the maize MnSODs are expressed and targeted into the mitochondrial matrix of transformed yeast cells.
我们最近证明,玉米线粒体锰超氧化物歧化酶(MnSODs)由一个差异表达的多基因家族编码。对克隆的玉米MnSod cDNA的分子特征分析表明,由克隆的MnSod编码的所有玉米MnSODs都具有线粒体转运肽,并且在所有MnSOD前体蛋白中基质靶向信号是保守的,这表明所有玉米MnSODs在体内都与线粒体相关。为了阐明每个玉米MnSOD在亚线粒体中的定位,将每个玉米MnSod cDNA导入MnSOD缺陷型酵母细胞中。在转化的酵母细胞中检测了每个MnSOD的功能作用和亚线粒体定位。在此,我们证明所有玉米MnSODs都可以在功能上弥补MnSOD的缺陷,并使转化的酵母细胞免受百草枯诱导的氧化应激。生化分析表明,所有玉米MnSODs都在转化的酵母细胞中表达并靶向线粒体基质。