Cloning of Arabidopsis thaliana phosphatidylinositol synthase and functional expression in the yeast pis mutant

被引:30
作者
Xue, HW
Hosaka, K
Plesch, G
Mueller-Roeber, B
机构
[1] Max Planck Inst Mol Plant Physiol, D-14476 Golm Potsdam, Germany
[2] Gunma Univ, Sch Hlth Sci, Dept Basic Allied Med, Maebashi, Gumma 3718514, Japan
关键词
Arabidopsis thaliana; molecular cloning; phosphatidylinositol synthase; signal transduction; yeast complementation;
D O I
10.1023/A:1006308909105
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
It is believed that phosphatidylinositol (PI) metabolism plays a central role in signalling pathways in both animals and higher plants. PI is synthesized from CDP-diacylglycerol (CDP-DG) and myo-inositol by phosphatidylinositol synthase (PI synthase, EC 2.7.8.11). Here we report the identification of a plant cDNA (AtPIS1) encoding a 26 kDa PI synthase from Arabidopsis thaliana. The plant enzyme as deduced from its cDNA sequence shares 35-41% identical amino acids with PI synthases from Saccharomyces cerevisiae and mammals. AtPIS1 functionally complements a mutant of S. cerevisiae with a lesion in PI synthase, and recombinant AtPIS1 protein present in yeast membranes strongly depends on the two principal substrates, myo-inositol and CDP-DG, and requires Mg2+ ions for full activity.
引用
收藏
页码:757 / 764
页数:8
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