首页> 外文期刊>Plant Molecular Biology >Ethylene biosynthetic genes are differentially expressed during carnation (Dianthus caryophyllus L.) flower senescence.
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Ethylene biosynthetic genes are differentially expressed during carnation (Dianthus caryophyllus L.) flower senescence.

机译:康乃馨(Dianthus caryophyllus L.)花衰老过程中乙烯生物合成基因的差异表达。

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Ethylene production and expression patterns of an 1-aminocyclopropane-1-carboxylic acid (ACC) oxidase (CARAO1) and of two ACC synthase genes (CARACC3 and CARAS1) were studied in floral organs of cut flowers of carnation 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; 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). They showed rapid cessation of ethylene production andgene 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.
机译:研究了香石竹切花的花器官中1-氨基环丙烷-1-甲酸(ACC)氧化酶(CARAO1)和两个ACC合酶基因(CARACC3和CARAS1)的乙烯产生和表达模式。白西姆在花瓶的生活中以及在用乙烯处理鲜花之后,首先在子房中开始产生乙烯并开始表达乙烯的生物合成基因,然后才是花柱和花瓣。 ACC氧化酶在所有花器官中都表达。在花瓶寿命中,观察到两个ACC合酶基因的组织特异性表达。用高乙烯浓度处理后,两个ACC合酶基因的组织特异性丧失,仅在表达上存在时间差异。在样式上,观察到乙烯生产与ACC合酶(CARAS1)基因表达之间的相关性较差,这表明活性在翻译水平上受到调节,或者CARAS1基因产物需要其他活性因子。从花瓣中分离出的花瓣在乙烯产量增加之前(第7天之前)显示,乙烯产量没有增加,乙烯生物合成基因的表达也没有增加。他们在花瓣乙烯生产的早期阶段(第7天)被切除时显示出乙烯生产和基因表达的快速停止,并且显示出乙烯生产和基因表达的模式类似于在第8天分离时在附着的花瓣中观察到的模式。讨论了基因表达的调控和乙烯在花衰老中作为信号分子。

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