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Sl-ERF2, a Tomato Ethylene Response Factor Involved in Ethylene Response and Seed Germination

机译:Sl-ERF2,涉及乙烯响应和种子萌发的番茄乙烯响应因子

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Ethylene response factors (ERFs) are plant transcriptional regulators mediating ethylene-dependent gene expression via binding to the GCC motif found in the promoter region of ethylene-regulated genes. We report here on the structural and functional characterization of the tomato Sl-ERF2 gene that belongs to a distinct class of the large ERF gene family. Both spliced and unspliced versions of Sl-ERF2 transcripts were amplified from RNA samples and the search in the public tomato expressed sequence tag (EST) database confirmed the existence of the two transcript species in a number of cDNA libraries. The unspliced transcript contains two open reading frames yielding two hypothetical proteins, a small highly truncated version lacking the APETALA2 domain and a bigger protein lacking the N-terminal MCGGAAII/L consensus peptide specific to ERF members from subfamily IV. Nevertheless, functional Sl-ERF2 protein may only derive from spliced transcripts since, depending on the tissue, the level of the spliced transcript is much higher than that of the unspliced transcript. Sl-ERF2 is expressed in all plant tissues tested, though its transcript accumulates preferentially in germinating seeds and ripening fruit. Overexpression of the Sl-ERF2 gene in transgenic tomato lines results in premature seed germination and enhanced hook formation of dark-grown seedlings, which is indicative of increased ethylene sensitivity. The expression of the mannanase2 gene is upregulated in Sl-ERF2-overexpressing seeds, suggesting that Sl-ERF2 stimulates seed germination through the induction of the mannanase2 gene. It is noteworthy that the exaggerated hook phenotype is abolished when ethylene perception is blocked, strongly suggesting that Sl-ERF2 requires other ethylene-dependent components to impact the hook formation process.
机译:乙烯反应因子(ERF)是植物转录调节因子,通过与乙烯调控基因的启动子区域中发现的GCC基序结合,介导乙烯依赖性基因表达。我们在这里报告的番茄Sl-ERF2基因的结构和功能表征,该基因属于大ERF基因家族的不同类别。从RNA样品中扩增出Sl-ERF2转录物的剪接和未剪接版本,并且在公共番茄表达序列标签(EST)数据库中的搜索证实了许多cDNA文库中两种转录物的存在。未剪接的转录本包含两个开放阅读框,产生两个假设的蛋白质,一个小的高度截短的版本缺少APETALA2结构域,一个更大的蛋白质缺少N末端MCGGAAI I / L 共有对亚家族IV的ERF成员特异的肽。然而,功能性的S1-ERF2蛋白可能仅来自剪接的转录本,因为取决于组织,剪接的转录本的水平比未剪接的转录本的水平高得多。 S1-ERF2在所有测试的植物组织中表达,尽管其转录本优先在发芽种子和成熟果实中积累。 Sl-ERF2基因在转基因番茄品系中的过表达导致种子过早发芽,并增加了深色幼苗的钩子形成,这表明乙烯敏感性增加。在过表达S1-ERF2的种子中,甘露聚糖酶2基因的表达被上调,表明S1-ERF2通过诱导甘露聚糖酶2基因来刺激种子萌发。值得注意的是,当阻止乙烯感知时,夸张的钩表型被消除,这强烈表明S1-ERF2需要其他依赖于乙烯的组分来影响钩形成过程。

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