Sablowski R W, Moyano E, Culianez-Macia F A, Schuch W, Martin C, Bevan M
Molecular Genetics Department John Innes Centre, Norwich, UK.
EMBO J. 1994 Jan 1;13(1):128-37. doi: 10.1002/j.1460-2075.1994.tb06242.x.
Synthesis of flavonoid pigments in flowers requires the co-ordinated expression of genes encoding enzymes in th phenylpropanoid biosynthetic pathway. Some cis-elements involved in the transcriptional control of these genes have been defined. We report binding of petal-specific activities from tobacco and Antirrhinum majus (snapdragon) to an element conserved in promoters of phenylpropanoid biosynthetic genes and implicated in expression in flowers. These binding activities were inhibited by antibodies raised against Myb305, a flower-specific Myb protein previously cloned from Antirrhinum by sequence homology. Myb305 bound to the same element and formed a DNA-protein complex with the same mobility as the Antirrhinum petal protein in electrophoretic mobility shift experiments. Myb305 activated expression from its binding site in yeast and in tobacco protoplasts. In protoplasts, activation also required a G-box-like element, suggesting co-operation with other elements and factors. The results strongly suggest a role for Myb305-related proteins in the activation of phenylpropanoid biosynthetic genes in flowers. This is consistent with the genetically demonstrated role of plant Myb proteins in the regulation of genes involved in flavonoid synthesis.
花朵中类黄酮色素的合成需要苯丙烷类生物合成途径中编码酶的基因协同表达。已确定了一些参与这些基因转录调控的顺式元件。我们报道了烟草和金鱼草花瓣特异性活性与苯丙烷类生物合成基因启动子中保守的一个元件的结合,该元件与花中的表达有关。这些结合活性被针对Myb305产生的抗体抑制,Myb305是一种先前通过序列同源性从金鱼草中克隆的花特异性Myb蛋白。在电泳迁移率变动实验中,Myb305与相同元件结合并形成了与金鱼草花瓣蛋白迁移率相同的DNA-蛋白质复合物。Myb305在酵母和烟草原生质体中从其结合位点激活表达。在原生质体中,激活还需要一个类G盒元件,这表明它与其他元件和因子存在协同作用。结果强烈表明Myb305相关蛋白在花中苯丙烷类生物合成基因的激活中起作用。这与遗传学证明的植物Myb蛋白在类黄酮合成相关基因调控中的作用一致。