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首页> 外文期刊>Plant and cell physiology >A Transcription Factor gamma MYB1 Binds to the P1BS cis-Element and Activates PLA(2)-gamma Expression with its Co-Activator gamma MYB2
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A Transcription Factor gamma MYB1 Binds to the P1BS cis-Element and Activates PLA(2)-gamma Expression with its Co-Activator gamma MYB2

机译:转录因子伽玛MYB1绑定到P1BS顺式元件,并激活PLA(2)-伽玛表达及其共激活因子伽玛MYB2。

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Phospholipase A(2) (PLA(2)) hydrolyzes phospholipid molecules to produce two products that are both precursors of second messengers of signaling pathways and signaling molecules per se. Arabidopsis thaliana PLA(2) paralogs (-beta, -gamma and -delta) play critical roles during pollen development, pollen germination and tube growth. In this study, analysis of the PLA(2)-gamma promoter using a deletion series revealed that the promoter region -153 to -1 is crucial for its pollen specificity. Using a yeast one-hybrid screening assay with the PLA(2)-gamma promoter and an Arabidopsis transcription factor (TF)-only library, we isolated two novel MYB-like TFs belonging to the MYB-CC family, denoted here as gamma MYB1 and gamma MYB2. By electrophoretic mobility shift assay, we found that these two TFs bind directly to the P1BS (phosphate starvation response 1-binding sequence) cis-element of the PLA(2)-gamma promoter. gamma MYB1 alone functioned as a transcriptional activator for PLA(2)-gamma expression, whereas gamma MYB2 directly interacted with gamma MYB1 and enhanced its activation. Overexpression of gamma MYB1 in the mature pollen grain led to increased expression of not only the PLA(2)-gamma gene but also of several genes whose promoters contain the P1BS cis-element and which are involved in the Pi starvation response, phospholipid biosynthesis and sugar synthesis. Based on these results, we suggest that the TF gamma MYB1 binds to the P1BS cis-element, activates the expression of PLA(2)-gamma with the assistance of its co-activator, gamma MYB2, and regulates the expression of several target genes involved in many plant metabolic reactions.
机译:磷脂酶A(2)(PLA(2))水解磷脂分子以产生两种产物,它们既是信号通路的第二信使的前体,又是信号分子本身。拟南芥PLA(2)旁系同源物(-beta,-gamma和-delta)在花粉发育,花粉萌发和管生长过程中起关键作用。在这项研究中,使用缺失序列对PLA(2)-γ启动子的分析显示,启动子区域-153至-1对于其花粉特异性至关重要。使用带有PLA(2)-γ启动子和拟南芥转录因子(TF)-仅库的酵母一杂交筛选测定法,我们分离了属于MYB-CC家族的两个新颖的MYB样TF,在这里称为γMYB1。和伽玛MYB2。通过电泳迁移率变动分析,我们发现这两个TF直接与PLA(2)-γ启动子的P1BS(磷酸饥饿响应1-结合序列)顺式元件结合。单独的伽玛MYB1充当PLA(2)-伽玛表达的转录激活因子,而伽玛MYB2直接与伽玛MYB1相互作用并增强其激活。在成熟的花粉粒中过表达γMYB1不仅导致PLA(2)-γ基因的表达增加,而且导致其启动子包含P1BS顺式元件且参与Pi饥饿反应,磷脂生物合成和糖合成。根据这些结果,我们建议TF伽马MYB1结合到P1BS顺式元件,借助其共激活因子伽马MYB2激活PLA(2)-γ的表达,并调节多个靶基因的表达参与许多植物代谢反应。

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