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调控矮牵牛花香产生的调控因子及其靶基因不仅在花瓣表皮细胞中具有活性。

Regulators of floral fragrance production and their target genes in petunia are not exclusively active in the epidermal cells of petals.

机构信息

Department of Plant Physiology, Swammerdam Institute for Life Sciences, University of Amsterdam, Science Park 904, 1098 XH Amsterdam, The Netherlands.

出版信息

J Exp Bot. 2012 May;63(8):3157-71. doi: 10.1093/jxb/ers034. Epub 2012 Feb 15.

Abstract

In which cells of the flower volatile biosynthesis takes place is unclear. In rose and snapdragon, some enzymes of the volatile phenylpropanoid/benzenoid pathway have been shown to be present in the epidermal cells of petals. It is therefore generally believed that the production of these compounds occurs in these cells. However, whether the entire pathway is active in these cells and whether it is exclusively active in these cells remains to be proven. Cell-specific transcription factors activating these genes will determine in which cells they are expressed. In petunia, the transcription factor EMISSION OF BENZENOIDS II (EOBII) activates the ODORANT1 (ODO1) promoter and the promoter of the biosynthetic gene isoeugenol synthase (IGS). The regulator ODO1 in turn activates the promoter of the shikimate gene 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS). Here the identification of a new target gene of ODO1, encoding an ABC transporter localized on the plasma membrane, PhABCG1, which is co-expressed with ODO1, is described. PhABCG1 expression is up-regulated in petals overexpressing ODO1 through activation of the PhABCG1 promoter. Interestingly, the ODO1, PhABCG1, and IGS promoters were active in petunia protoplasts originating from both epidermal and mesophyll cell layers of the petal, suggesting that the volatile phenylpropanoid/benzenoid pathway in petunia is active in these different cell types. Since volatile release occurs from epidermal cells, trafficking of (volatile) compounds between cell layers must be involved, but the exact function of PhABCG1 remains to be resolved.

摘要

在花中哪些细胞参与挥发性生物合成尚不清楚。在玫瑰和金鱼草中,一些挥发性苯丙烷/苯并呋喃途径的酶已被证明存在于花瓣的表皮细胞中。因此,人们普遍认为这些化合物是在这些细胞中产生的。然而,这些细胞中是否存在整个途径以及该途径是否仅在这些细胞中活跃,仍有待证明。激活这些基因的细胞特异性转录因子将决定它们在哪些细胞中表达。在矮牵牛中,转录因子苯丙烷/苯并呋喃的排放 II(EOBII)激活了气味素 1(ODO1)启动子和生物合成基因异丁香酚合酶(IGS)的启动子。调节因子 ODO1 反过来又激活了莽草酸基因 5-烯醇丙酮酰莽草酸-3-磷酸合酶(EPSPS)的启动子。在这里,描述了 ODO1 的一个新靶基因的鉴定,该基因编码一种 ABC 转运蛋白,定位于质膜上,PhABCG1,它与 ODO1 共表达。PhABCG1 的表达在过表达 ODO1 的花瓣中原生质体中上调,这是通过 PhABCG1 启动子的激活实现的。有趣的是,ODO1、PhABCG1 和 IGS 启动子在源自花瓣表皮和叶肉细胞层的矮牵牛原生质体中均具有活性,这表明矮牵牛中的挥发性苯丙烷/苯并呋喃途径在这些不同的细胞类型中均具有活性。由于挥发性物质是从表皮细胞释放的,因此必须涉及化合物在细胞层之间的运输,但 PhABCG1 的确切功能仍有待解决。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4bd/3350925/2fe6f9521c97/jexboters034f01_3c.jpg

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