Li Yong-Fu, Shi Feng
The Key Laboratory of Industrial Biotechnology, Ministry of Education, Southern Yangtze University, Wuxi 214036, China.
Acta Biochim Biophys Sin (Shanghai). 2006 May;38(5):293-8. doi: 10.1111/j.1745-7270.2006.00162.x.
Three NAD kinase homologs, encoded by UTR1, POS5 and YEF1 genes, are found in the yeast Saccharomyces cerevisiae and proven to be important sources of NADPH for the cell. Pos5p, existing in the mitochondrial matrix, is critical for higher temperature endurance and mitochondrial functions, such as glycerol usability and arginine biosynthesis. Through constructing the high-copy expression plasmids of YEF1 and UTR1, which contained the green fluorescent protein reporter tag at their 3' terminus, and introducing them into POS5 gene deletion mutants (i.e. pos5, utr1pos5, yef1pos5 and utr1yef1pos5), the high-copy YEF1 and UTR1 plasmids carrying transformants for pos5 mutants were obtained. Their temperature sensitivity and growth phenotype on media with glycerol as the sole carbon source, or on media without arginine, were checked. Results showed the partial rescue of mitochondrial dysfunctions and temperature sensitivity of pos5 mutants by the high-copy YEF1 gene, and of glycerol growth defect and temperature sensitivity by the high-copy UTR1 gene, which confirmed the potential supplying ability of Yef1p and Utr1p for mitochondrial NADP(H) and implied the weak transport of NADP from cytosol to mitochondria. However, even through the green fluorescent protein reporter label, the subcellular localization of Yef1p and Utr1p in yeast cells could not be observed, which indicated the low expression level of these two NAD kinase homologs.
在酿酒酵母中发现了由UTR1、POS5和YEF1基因编码的三种NAD激酶同源物,它们被证明是细胞中NADPH的重要来源。存在于线粒体基质中的Pos5p对于较高温度耐受性和线粒体功能(如甘油可用性和精氨酸生物合成)至关重要。通过构建YEF1和UTR1的高拷贝表达质粒(它们在3'末端含有绿色荧光蛋白报告标签),并将它们导入POS5基因缺失突变体(即pos5、utr1pos5、yef1pos5和utr1yef1pos5),获得了携带pos5突变体转化子的高拷贝YEF1和UTR1质粒。检测了它们在以甘油为唯一碳源的培养基上或不含精氨酸的培养基上的温度敏感性和生长表型。结果表明,高拷贝YEF1基因部分挽救了pos5突变体的线粒体功能障碍和温度敏感性,高拷贝UTR1基因部分挽救了甘油生长缺陷和温度敏感性,这证实了Yef1p和Utr1p对线粒体NADP(H)的潜在供应能力,并暗示了NADP从细胞质到线粒体的弱转运。然而,即使通过绿色荧光蛋白报告标签,也无法观察到Yef1p和Utr1p在酵母细胞中的亚细胞定位,这表明这两种NAD激酶同源物的表达水平较低。