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Regulation of Senescence-Related Gene Expression in Carnation Flower Petals by Ethylene

机译:乙烯对康乃馨花瓣中衰老相关基因表达的调控

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摘要

Ethylene plays a regulatory role in carnation (Dianthus caryophyllus L.) flower senescence. Petal senescence coincides with a burst of ethylene production, is induced prematurely in response to exogenous ethylene, and is delayed by inhibitors of ethylene biosynthesis or action. We have investigated the role of ethylene in the regulation of three senescence-related cDNA clones isolated from a senescent carnation petal library (KA Lawton et al. [1989] Plant Physiol 90: 690-696). Expression of two of the cloned mRNAs in response to ethylene is floral specific, while the expression of another mRNA can be induced in both leaves and flowers exposed to ethylene. Although ethylene induces expression of these mRNAs in petals, message abundance decreases when flowers are removed from ethylene unless an autoenhancement of ethylene production is induced. This indicates continued perception of ethylene is required for their expression. Interruption of ethylene action following the onset of natural senescence results in a substantial decrease in transcript abundance of two of these mRNAs. However, the abundance of another mRNA remains unaffected, indicating this gene responds to temporal cues as well as to ethylene. As flowers age the dosage of exogenous ethylene required to induce expression of the cloned mRNAs decreases, indicating sensitivity to ethylene changes as the tissue matures. Nuclear run-on transcription experiments indicate that relative transcription rates of cloned mRNAs increase in response to exogenous ethylene.
机译:乙烯在康乃馨(Dianthus caryophyllus L.)花衰老中起调节作用。花瓣衰老与乙烯的爆发同时发生,是响应于外源乙烯过早地诱导的,并且被乙烯生物合成或作用的抑制剂所延迟。我们已经研究了乙烯在调节从衰老康乃馨花瓣文库中分离的三个衰老相关的cDNA克隆中的作用(KA Lawton等人,[1989] Plant Physiol 90:690-696)。响应乙烯,两个克隆的mRNA的表达具有花卉特异性,而暴露于乙烯的叶子和花朵均可诱导另一种mRNA的表达。尽管乙烯会诱导花瓣中这些mRNA的表达,但是当从乙烯中去除花时,除非诱导了乙烯产量的自动增强,否则消息的丰度会降低。这表明对它们的表达需要持续感知乙烯。自然衰老开始后乙烯作用的中断导致其中两个mRNA的转录丰度大大降低。但是,另一种mRNA的丰度仍然不受影响,表明该基因对时间线索以及乙烯都有反应。随着花龄的增长,诱导克隆的mRNA表达所需的外源乙烯的剂量减少,表明对乙烯的敏感性随着组织的成熟而变化。核运行转录实验表明,克隆的mRNA的相对转录速率响应于外源乙烯而增加。

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