首页> 外文期刊>Plant Biotechnology Journal >The strawberry transcription factor FaRAV1 positively regulates anthocyanin accumulation by activation of FaMYB10 and anthocyanin pathway genes
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The strawberry transcription factor FaRAV1 positively regulates anthocyanin accumulation by activation of FaMYB10 and anthocyanin pathway genes

机译:草莓转录因子Farav1通过激活FamyB10和花青素途径基因来积正调节花青素积累

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The RAV (related to ABI3/viviparous 1) group of transcription factors (TFs) play multifaceted roles in plant development and stress responses. Here, we show that strawberry (Fragaria?×?ananassa) FaRAV1 positively regulates anthocyanin accumulation during fruit ripening via a hierarchy of activation processes. Dual‐luciferase assay screening of all fruit‐expressed AP2/ERFs showed FaRAV1 had the highest transcriptional activation of the promoter of FaMYB10, a key activator of anthocyanin biosynthesis. Yeast one‐hybrid and electrophoretic mobility shift assays indicated that FaRAV1 could directly bind to the promoter of FaMYB10. Transient overexpression of FaRAV1 in strawberry fruit increased FaMYB10 expression and anthocyanin production significantly. Correspondingly, transient RNA interference‐induced silencing of FaRAV1 led to decreases in FaMYB10 expression and anthocyanin content. Transcriptome analysis of FaRAV1‐overexpressing strawberry fruit revealed that transcripts of phenylpropanoid and flavonoid biosynthesis pathway genes were up‐regulated. Luciferase assays showed that FaRAV1 could also activate the promoters of strawberry anthocyanin biosynthetic genes directly, revealing a second level of FaRAV1 action in promoting anthocyanin accumulation. These results show that FaRAV1 stimulates anthocyanin accumulation in strawberry both by direct activation of anthocyanin pathway gene promoters and by up‐regulation of FaMYB10, which also positively regulates these genes.
机译:RAV(与ABI3 / Viviparous 1)的转录因子组(TFS)在植物开发和应力反应中起多方刻录作用。在这里,我们展示了草莓(Fragaria?×?ananassa)Farav1在通过激活过程的层次结构上积极地调节果实成熟过程中的花青素积累。所有果实表达的AP2 / ERF的双荧光素酶测定筛选筛选Farav1具有最高的FamyB10启动子的转录激活,是花青素生物合成的关键活化剂。酵母单杂交和电泳迁移率移位测定表明,Farav1可以直接与FamyB10的启动子结合。 Farav1在草莓果上的瞬时过度表达增加了FamyB10表达和花青素的产生显着。相应地,FaraV1的瞬时RNA干扰引起的沉默导致FamyB10表达和花青素含量降低。 Farav1过度表达草莓果的转录组分析显示,上调苯丙醇和黄酮类生物合成途径基因的转录物。荧光素酶测定表明,Farav1还可以直接激活草莓花青素生物合成基因的启动子,揭示了促进花青素积累中的Farav1作用的第二级。这些结果表明,Farav1通过直接激活花青素途径基因启动子并通过对FamyB10的上调来刺激草莓中的花青素积累,这也积极调节这些基因。

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