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Activation of the Maize Anthocyanin Gene a2 Is Mediated by an Element Conserved in Many Anthocyanin Promoters

机译:玉米花色苷基因a2的激活 由许多花色苷中保守的元素介导 发起人

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摘要

Two transcription factors, C1 (a Myb-domain protein) and B (a basic-helix-loop-helix protein), mediate transcriptional activation of the anthocyanin-biosynthetic genes of maize (Zea mays). To begin to assess the mechanism of activation, the sequences required for C1- and B-mediated induction have been determined for the a2 promoter, which encodes an anthocyanin-biosynthetic enzyme. Analysis of a series of 7- to 13-base-pair substitutions revealed two regions crucial for activation. One region, centered at −99, contained a C1-binding site that abolished C1 binding. The other crucial region was adjacent, centered at −91. C1 binding was not detected at this site, and mutation of this site did not prevent C1 binding at −99. An oligonucleotide dimer containing these two crucial elements was sufficient for C1 and B activation of a heterologous promoter. These data suggest that activation of the anthocyanin genes involves C1 and another factor binding at closely adjacent sites. Mutating a previously postulated anthocyanin consensus sequence within a2 did not significantly reduce activation by C1 and B. However, sequence comparisons of the crucial a2 regions with sequences important for C1- and B-mediated activation in two other anthocyanin promoters led to a revised consensus element shared by these promoters.
机译:两个转录因子,C1(一种Myb结构域蛋白)和B(一种基本螺旋-环-螺旋蛋白),介导了玉米(Zea mays)花色苷生物合成基因的转录激活。为了开始评估激活机制,已经确定了a1启动子的C1和B介导的诱导序列,该启动子编码花青素生物合成酶。对一系列7至13个碱基对的取代进行分析后发现,两个区域对于激活至关重要。以-99为中心的一个区域包含一个C1结合位点,该位点废除了C1结合。另一个关键区域是相邻的,以-91为中心。在该位点未检测到C1结合,并且该位点的突变并未阻止-99处的C1结合。包含这两个关键元件的寡核苷酸二聚体足以激活异源启动子的C1和B。这些数据表明,花色素苷基因的激活涉及C1和另一个紧密结合位点的因子结合。突变先前假定的花色苷共有序列 a2并未显着降低C1和B的激活。 但是,关键a2区的序列比较 与其他两个对C1和B介导的激活重要的序列 花青素启动子导致了由 这些发起人。

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