ten Have A, Woltering E J
Agrotechnological Research Institute (ATO-DLO), Wageningen, Netherlands.
Plant Mol Biol. 1997 May;34(1):89-97. doi: 10.1023/a:1005894703444.
Ethylene production and expression patterns of an 1-aminocyclopropane-1-carboxylic acid (ACC) oxidase (CARAO1) and of two ACC synthase (EC 4.4.1.14) genes (CARACC3 and CARAS1) were studied in floral organs of cut carnation flowers (Dianthus caryophyllus L.) cv. White Sim. During the vase life and after treatment of fresh flowers with ethylene, production of ethylene and expression of ethylene biosynthetic genes first started in the ovary followed by the styles and the petals. ACC oxidase was expressed in all the floral organs whereas, during the vase life, tissue-specific expression of the two ACC synthase genes was observed. After treatment with a high ethylene concentration, tissue specificity of the two ACC synthase genes was lost and only a temporal difference in expression remained. In styles, poor correlation between ethylene production and ACC synthase (CARAS1) gene expression was observed suggesting that either activity is regulated at the translational level or that the CARAS1 gene product requires an additional factor for activity. Isolated petals showed no increase in ethylene production and expression of ethylene biosynthetic genes when excised from the flower before the increase in petal ethylene production (before day 7); showed rapid cessation of ethylene production and gene expression when excised during the early phase of petal ethylene production (day 7) and showed a pattern of ethylene production and gene expression similar to the pattern observed in the attached petals when isolated at day 8. The interorgan regulation of gene expression and ethylene as a signal molecule in flower senescence are discussed.
在香石竹(Dianthus caryophyllus L.)品种“White Sim”的切花的花器官中,研究了乙烯生成以及1-氨基环丙烷-1-羧酸(ACC)氧化酶(CARAO1)和两个ACC合成酶(EC 4.4.1.14)基因(CARACC3和CARAS1)的表达模式。在瓶插寿命期间以及用乙烯处理鲜花后,乙烯生成以及乙烯生物合成基因的表达首先在子房开始,随后是花柱和花瓣。ACC氧化酶在所有花器官中均有表达,而在瓶插寿命期间,观察到两个ACC合成酶基因的组织特异性表达。用高浓度乙烯处理后,两个ACC合成酶基因的组织特异性丧失,仅保留表达上的时间差异。在花柱中,观察到乙烯生成与ACC合成酶(CARAS1)基因表达之间相关性较差,这表明要么活性在翻译水平受到调控,要么CARAS1基因产物需要额外的因子来激活。从花朵上切下的花瓣,在花瓣乙烯生成增加之前(第7天之前)切下时,乙烯生成和乙烯生物合成基因的表达没有增加;在花瓣乙烯生成早期(第7天)切下时,乙烯生成和基因表达迅速停止;在第8天切下时,乙烯生成和基因表达模式与附着花瓣中观察到的模式相似。本文讨论了基因表达的器官间调控以及乙烯作为花衰老中的信号分子的作用。