首页> 外文期刊>African Journal of Plant Science >Functional analysis of the UDP glucose: Flavonoid-3-Oglucosyltransferase (UFGT) promoter from litchi (Litchi chinesis Sonn.) and transient expression in onions (Allium cepa Linn.)
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Functional analysis of the UDP glucose: Flavonoid-3-Oglucosyltransferase (UFGT) promoter from litchi (Litchi chinesis Sonn.) and transient expression in onions (Allium cepa Linn.)

机译:UDP葡萄糖的功能分析:荔枝(Litchi chinesis Sonn。)的类黄酮3-O葡萄糖基转移酶(UFGT)启动子和洋葱(葱属)的瞬时表达

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The expression of the UDP glucose: flavonoid-3-Oglucosyltransferase (UFGT), which encoded the last enzyme of the anthocyanin pathway, was under developmental control as well as affected by external stimuli such as ABA. Three fragments of the 1.38 kb upstream region of the UFGT gene from Litchi (Litchi chinesis Sonn.) were fused to the GUS-coding region, and the expression of these constructs was analyzed in onions. To characterize the cis-regulatory functions of the promoters for enzymes in anthocyanin biosynthesis, we examined onions carrying a series of nested UFGT promoter-β-glucuronidase (GUS) fusion for GUS activity by histochemical staining. The AE-box and ELI-box in anthocyanin biosynthesis of angiosperm were found in UFGT promoter. MRE which was MYB binding site involved in light responsiveness, control the transcription of genes in anthocyanin biosynthesis. The region of -910 to -344 in UFGT promoter showed high activities in the three parts. Although the expression characteristics were indistinguishable from those of the full-length promoter, we observed differences in UFGT promoter regulation for the different construct. The results suggested that region of 910 to 344 of UFGT promoter had multiple functions in the expression under the various developmental stages and stress conditions in litchi.
机译:UDP糖:类黄酮-3-O葡糖基转移酶(UFGT)的编码受花青素途径的最后一种酶的表达受到发育控制,并受到外部刺激(例如ABA)的影响。将来自荔枝(Litchi chinesis Sonn。)的UFGT基因的1.38 kb上游区域的三个片段融合到GUS编码区,并在洋葱中分析了这些构建体的表达。为了表征花青素生物合成中酶的启动子的顺式调节功能,我们通过组织化学染色检查了带有一系列嵌套式UFGT启动子-β-葡萄糖醛酸苷酶(GUS)融合的洋葱的GUS活性。在UFGT启动子中发现了被子植物花青素生物合成中的AE-box和ELI-box。 MRE是MYB结合位点,参与光响应,控制花色苷生物合成中的基因转录。 UFGT启动子中的-910至-344区域在这三个部分均显示高活性。尽管表达特征与全长启动子没有区别,但是我们观察到了不同构建体的UFGT启动子调控的差异。结果表明,在荔枝不同发育阶段和胁迫条件下,UFGT启动子910-344区域具有多种表达功能。

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