Huang J, Lee S H, Lin C, Medici R, Hack E, Myers A M
Department of Genetics, Iowa State University, Ames 50011.
EMBO J. 1990 Feb;9(2):339-47. doi: 10.1002/j.1460-2075.1990.tb08116.x.
The mitochondrial gene T-urf13 from maize (Zea mays L.) with Texas male-sterile (T) cytoplasm codes for a unique 13 kd polypeptide, T-URF13, which is implicated in cytoplasmic male sterility and sensitivity to the insecticide methomyl and to host-specific fungal toxins produced by Helminthosporium maydis race T (HmT toxin) and Phyllosticta maydis (Pm toxin). A chimeric gene coding for T-URF13 fused to the mitochondrial targeting peptide from the Neurospora crassa ATP synthase subunit 9 precursor was constructed. Expression of this gene in the yeast Saccharomyces cerevisiae yielded a polypeptide that was translocated into the membrane fraction of mitochondria and processed to give a protein the same size as maize T-URF13. Methomyl, HmT toxin and Pm toxin inhibited growth of yeast cells expressing the gene fusion on medium containing glycerol as sole carbon source and stimulated respiration with NADH as substrate by isolated mitochondria from these cells. These effects were not observed in yeast cells expressing T-URF13 without a targeting peptide. The results show that T-URF13 is sufficient to confer sensitivity to methomyl and the fungal toxins in a heterologous eukaryotic system, and suggest that mitochondrial localization of T-URF13 is critical for these functions.
来自玉米(Zea mays L.)且具有德州雄性不育(T)细胞质的线粒体基因T-urf13编码一种独特的13kd多肽T-URF13,该多肽与细胞质雄性不育以及对杀虫剂灭多威、玉米小斑病菌T小种(HmT毒素)和玉米叶点霉(Pm毒素)产生的宿主特异性真菌毒素的敏感性有关。构建了一个嵌合基因,该基因编码与来自粗糙脉孢菌ATP合酶亚基9前体的线粒体靶向肽融合的T-URF13。该基因在酿酒酵母中的表达产生了一种多肽,该多肽被转运到线粒体的膜部分并被加工成与玉米T-URF13大小相同的蛋白质。灭多威、HmT毒素和Pm毒素抑制了在以甘油作为唯一碳源的培养基上表达基因融合体的酵母细胞的生长,并刺激了来自这些细胞的分离线粒体以NADH作为底物的呼吸作用。在不表达具有靶向肽的T-URF13的酵母细胞中未观察到这些效应。结果表明,T-URF13足以在异源真核系统中赋予对灭多威和真菌毒素的敏感性,并表明T-URF13的线粒体定位对于这些功能至关重要。