Costa C L, Arruda P, Benedetti C E
Centro de Biologia Molecular e Engenharia Genética, Universidade Estadual de Campinas, SP, Brazil.
Plant Mol Biol. 2000 Sep;44(1):61-71. doi: 10.1023/a:1006464822434.
The regulation of genes in response to wounding is mediated in part by the octadecanoids 12-oxo-phytodienoic acid (OPDA), jasmonic acid (JA) and its methyl ester methyl jasmonate (MeJA). We identified, by differential display, an Arabidopsis gene (OPR3) induced after wounding. OPR3 is homologous to members of the flavin mononucleotide (FMN) binding proteins, including the old yellow enzyme (OYE) from yeast and 12-oxophytodienoate-10,11-reductase (OPR) from Arabidopsis. Transcripts of OPR3 rapidly accumulated in leaves after wounding and MeJA treatment, but they were detected in various tissues of unwounded plants at relatively low levels. Expression of the OPR3 gene was significantly reduced in wounded leaves of the coil mutant, indicating partial dependence on jasmonate perception for full induction of the gene. The recombinant protein of OPR3 cross-reacted with an antiserum raised against the OYE protein, and showed oxidation of beta-NADPH when OPDA or 15-deoxy-delta(12,14) prostaglandin J2 (PGJ2), an analogue of OPDA, was used as substrate. Beta-NADPH oxidation was not observed when MeJA, which lacks the double bond in the ketone ring, was used as substrate. The recombinant OPR3 protein also showed beta-NADPH oxidation activity in the presence of cyclohexenone, but not cyclohexanone, suggesting that the enzyme has specificity to cleavage of olefinic bonds in cyclic enones. The results show that the OPR3 gene product represents a new OPR of Arabidopsis induced after wounding.
基因对创伤的响应调节部分是由十八烷类物质12-氧代-植物二烯酸(OPDA)、茉莉酸(JA)及其甲酯茉莉酸甲酯(MeJA)介导的。我们通过差异显示法鉴定出一个在创伤后被诱导的拟南芥基因(OPR3)。OPR3与黄素单核苷酸(FMN)结合蛋白家族成员同源,包括酵母中的老黄色酶(OYE)和拟南芥中的12-氧代植物二烯酸-10,11-还原酶(OPR)。创伤和MeJA处理后,OPR3的转录本在叶片中迅速积累,但在未受伤植物的各种组织中检测到的水平相对较低。在coil突变体的受伤叶片中,OPR3基因的表达显著降低,表明该基因的完全诱导部分依赖于茉莉酸的感知。OPR3的重组蛋白与针对OYE蛋白产生的抗血清发生交叉反应,当使用OPDA或15-脱氧-δ(12,14)前列腺素J2(PGJ2,OPDA的类似物)作为底物时,显示出β-NADPH的氧化。当使用在酮环中缺乏双键的MeJA作为底物时,未观察到β-NADPH氧化。重组OPR3蛋白在环己烯酮存在下也显示出β-NADPH氧化活性,但在环己酮存在下则没有,这表明该酶对环状烯酮中烯烃键的裂解具有特异性。结果表明,OPR3基因产物代表了拟南芥中一种创伤后诱导的新型OPR。