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首页> 外文期刊>Plant physiology >Characterization of GaWRKY1, a cotton transcription factor that regulates the sesquiterpene synthase gene (+)-delta-cadinene synthase-A
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Characterization of GaWRKY1, a cotton transcription factor that regulates the sesquiterpene synthase gene (+)-delta-cadinene synthase-A

机译:GaWRKY1的特征,棉花转录因子调节倍半萜烯合酶基因(+)-δ-cad烯合酶-A

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摘要

The cotton (+)-delta-cadinene synthase (CAD1), a sesquiterpene cyclase, catalyzes a branch-point step leading to biosynthesis of sesquiterpene phytoalexins, including gossypol. CAD1-A is a member of CAD1 gene family, and its promoter contains a W-box palindrome with two reversely oriented TGAC repeats, which are the proposed binding sites of WRKY transcription factors. We isolated several WRKY cDNAs from Gossypium arboreum. One of them, GaWRKY1, encodes a protein containing a single WRKY domain and a putative N-terminal Leu zipper. Similar to genes encoding enzymes of cotton sesquiterpene pathway, GaWRKY1 was down-regulated in a glandless cotton cultivar that contained much less gossypol. GaWRKY1 showed a temporal and spatial pattern of expression comparable to that of CAD1-A in various aerial organs examined, including sepal, stigma, anther, and developing seeds. In suspension cells, expression of both GaWRKY1 and CAD1-A genes and biosynthesis of sesquiterpene aldehydes were strongly induced by a fungal elicitor preparation and methyl jasmonate. GaWRKY1 interacted with the 3 x W-box derived from CAD1-A promoter in yeast (Saccharomyces cerevisiae) one-hybrid system and in vitro. Furthermore, in transgenic Arabidopsis plants, overexpression of GaWRKY1 highly activated the CAD1-A promoter, and transient assay in tobacco (Nicotiana tabacum) leaves demonstrated that W-box was required for this activation. These results suggest that GaWRKY1 participates in regulation of sesquiterpene biosynthesis in cotton, and CAD1-A is a target gene of this transcription factor.
机译:棉(+)-δ-卡丹烯合酶(CAD1)是倍半萜环化酶,它催化了一个分支点,从而导致了倍半萜植物抗毒素(包括棉酚)的生物合成。 CAD1-A是CAD1基因家族的成员,其启动子包含W-box回文,带有两个反向TGAC重复序列,这是WRKY转录因子的拟议结合位点。我们从植物棉中分离了几个WRKY cDNA。其中之一,GaWRKY1,编码包含单个WRKY域和一个假定的N末端Leu拉链的蛋白质。与编码棉倍半萜途径的酶的基因相似,GaWRKY1在含有少得多的棉酚的无腺棉花品种中被下调。 GaWRKY1在所检查的各种气生器官(包括萼片,柱头,花药和发育中的种子)中表现出与CAD1-A相当的时空表达模式。在悬浮细胞中,真菌诱导剂制剂和茉莉酸甲酯强烈诱导了GaWRKY1和CAD1-A基因的表达以及倍半萜醛的生物合成。 GaWRKY1与酵母(Saccharomyces cerevisiae)单杂交系统中的CAD1-A启动子衍生的3 x W-box相互作用,并在体外相互作用。此外,在转基因拟南芥植物中,GaWRKY1的过表达高度激活了CAD1-A启动子,并且在烟草(烟草)叶片中进行瞬时分析表明,这种激活需要W-box。这些结果表明,GaWRKY1参与棉花中倍半萜生物合成的调节,而CAD1-A是该转录因子的靶基因。

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