Norris S R, Shen X, DellaPenna D
Department of Biochemistry and Plant Sciences, University of Arizona, Tucson, Arizona 85721, USA.
Plant Physiol. 1998 Aug;117(4):1317-23. doi: 10.1104/pp.117.4.1317.
Plastoquinone and tocopherols are the two major quinone compounds in higher plant chloroplasts and are synthesized by a common pathway. In previous studies we characterized two loci in Arabidopsis defining key steps of this biosynthetic pathway. Mutation of the PDS1 locus disrupts the activity of p-hydroxyphenylpyruvate dioxygenase (HPPDase), the first committed step in the synthesis of both plastoquinone and tocopherols in plants. Although plants homozygous for the pds1 mutation could be rescued by growth in the presence of homogentisic acid, the product of HPPDase, we were unable to determine if the mutation directly or indirectly disrupted HPPDase activity. This paper reports the isolation of a cDNA, pHPPD, encoding Arabidopsis HPPDase and its functional characterization by expression in both plants and Escherichia coli. pHPPD encodes a 50-kD polypeptide with homology to previously identified HPPDases, including 37 highly conserved amino acid residues clustered in the carboxyl region of the protein. Expression of pHPPD in E. coli catalyzes the accumulation of homogentisic acid, indicating that it encodes a functional HPPDase enzyme. Mapping of pHPPD and co-segregation analysis of the pds1 mutation and the HPPD gene indicate tight linkage. Constitutive expression of pHPPD in a pds1 mutant background complements this mutation. Finally, comparison of the HPPD genomic sequences from wild type and pds1 identified a 17-bp deletion in the pds1 allele that results in deletion of the carboxyterminal 26 amino acids of the HPPDase protein. Together, these data conclusively demonstrate that pds1 is a mutation in the HPPDase structural gene.
质体醌和生育酚是高等植物叶绿体中的两种主要醌类化合物,它们通过共同途径合成。在先前的研究中,我们对拟南芥中的两个基因座进行了表征,确定了该生物合成途径的关键步骤。PDS1基因座的突变破坏了对羟基苯丙酮酸双加氧酶(HPPDase)的活性,这是植物中质体醌和生育酚合成的第一个关键步骤。尽管pds1突变的纯合植物可以通过在尿黑酸(HPPDase的产物)存在下生长来挽救,但我们无法确定该突变是直接还是间接破坏了HPPDase的活性。本文报道了一个编码拟南芥HPPDase的cDNA(pHPPD)的分离及其在植物和大肠杆菌中的表达功能表征。pHPPD编码一个50kD的多肽,与先前鉴定的HPPDase具有同源性,包括在蛋白质羧基区域聚集的37个高度保守的氨基酸残基。pHPPD在大肠杆菌中的表达催化尿黑酸的积累,表明它编码一种功能性的HPPDase酶。pHPPD的定位以及pds1突变与HPPD基因的共分离分析表明它们紧密连锁。在pds1突变体背景下组成型表达pHPPD可弥补该突变。最后,对野生型和pds1的HPPD基因组序列进行比较,发现在pds1等位基因中有一个17bp的缺失,导致HPPDase蛋白的羧基末端26个氨基酸缺失。这些数据共同确凿地证明pds1是HPPDase结构基因中的一个突变。