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The MYB305 Transcription Factor Regulates Expression of Nectarin Genes in the Ornamental Tobacco Floral Nectary

机译:MYB305转录因子调节油桃花蜜中油桃基因的表达。

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摘要

We have isolated and characterized the cDNA encoding the ornamental tobacco (Nicotiana langsdorffii X N. sanderae) homolog of the antirrhinum (Antirrhinum majus) MYB305. This transcription factor was robustly expressed at Stage 12 of nectary development but was only weakly expressed in the earlier Stage 6 nectaries. The ornamental tobacco MYB305 contains a conserved R2R3 MYB DNA binding domain with 76 amino acids in the activation domain. A green fluorescent protein-MYB305 fusion localized to nucleus of tobacco protoplasts and yeast one-hybrid assays demonstrated that it functions as a transcription activator. A conserved 23–amino acid C-terminal domain is required to activate gene expression. The coding region of the myb305 cDNA was expressed in Escherichia coli as a glutathione S-transferase fusion protein and was purified to homogeneity. This protein shows binding to two consensus MYB binding sites on the ornamental tobacco Nectarin I (nec1) promoter as well as to the single site located on the Nectarin V (nec5) promoter. Deletions of either of the binding sites from the nec1 promoter significantly reduced expression in nectary tissues. Temporally, MYB305 expression precedes that of nec1 and nec5, as would be expected if the MYB305 factor regulates expression of the nec1 and nec5 genes. Ectopic expression of MYB305 in foliage was able to induce expression of both nec1 and nec5, as well as two flavonoid biosynthetic genes in the foliage. Finally, RNA interference knockdown of MYB305 resulted in reduced expression of both nectarins and flavonoid biosynthetic genes. We conclude that expression of MYB305 regulates expression of the major nectarin genes in the floral nectary.
机译:我们已经分离和表征了编码抗大黄(Antirrhinum majus)MYB305的观赏烟草(Nicotiana langsdorffii X N. sanderae)同源物的cDNA。该转录因子在蜜腺发育的第12阶段强烈表达,但在较早的第6阶段蜜腺中仅弱表达。观赏烟草MYB305包含一个保守的R2R3 MYB DNA结合结构域,在激活结构域中具有76个氨基酸。定位于烟草原生质体核的绿色荧光蛋白-MYB305融合蛋白和酵母一杂交实验表明,它可作为转录激活因子。需要保守的23个氨基酸的C末端域来激活基因表达。 myb305 cDNA的编码区作为谷胱甘肽S-转移酶融合蛋白在大肠杆菌中表达,并纯化至均一。此蛋白显示出与观赏烟草油桃I(nec1)启动子上的两个共有MYB结合位点以及位于油桃V(nec5)启动子上的单个位点的结合。从nec1启动子中删除两个结合位点中的一个,将大大减少在蜜腺组织中的表达。暂时地,MYB305的表达先于nec1和nec5的表达,如MYB305因子调节nec1和nec5基因的表达所预期的那样。 MYB305在叶中的异位表达能够诱导nec1和nec5以及叶中两个类黄酮生物合成基因的表达。最后,MYB305的RNA干扰抑制导致油桃和类黄酮生物合成基因的表达降低。我们得出结论,MYB305的表达调节花蜜中主要油桃基因的表达。

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