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Viviparous1 alters global gene expression patterns through regulation of abscisic acid signaling [Review]

机译:Viviparous1通过调节脱落酸信号传导改变整体基因表达模式[综述]

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摘要

Maize (Zea mays) Viviparous1 (VP1) and Arabidopsis ABI3 are orthologous transcription factors that regulate key aspects of plant seed development and ABA signaling. To understand VP1-regulated gene expression on a global scale, we have performed oligomicroarray analysis of transgenic Arabidopsis carrying 35S::VP1 in an abi3 null mutant background. We have identified 353 VP1/ABA-regulated genes by GeneChip analysis. Seventy-three percent of the genes were affected by both VP1 and ABA in vegetative tissues, indicating a tight coupling between ABA signaling and VP1 function. A large number of seed-specific genes were ectopically expressed in vegetative tissue of 35S::VP1 plants consistent with evidence that VP1 and ABI3 are key determinants of seed-specific expression. ABI5, a positive regulator of ABA signaling, was activated by VP1, indicating conservation of the feed-forward pathway mediated by ABI3. ABA induction of ABI1 and ABI2, negative regulators of ABA signaling, was strongly inhibited by VP1, revealing a second pathway of feed-forward regulation. These results indicate that VP1 strongly modifies ABA signaling through feed-forward regulation of ABI1/ABI5-related genes. Of the 32 bZIP transcription factors represented on the GeneChip, genes in the ABI5 clade were specifically coregulated by ABA and VP1. Statistical analysis of 5' upstream sequences of the VP1/ABA-regulated genes identified consensus abscisic responsive elements as an enriched element, indicating that many of the genes could be direct targets of the ABI5-related bZIPs. The Sph element is an enriched sequence motif in promoters of genes co-activated by ABA and VP1 but not in promoters of genes activated by ABA alone. This analysis reveals that distinct combinatorial patterns of promoter elements distinguish subclasses of VP1/ABA coregulated genes.
机译:玉米(Zea mays)Viviparous1(VP1)和拟南芥ABI3是直系同源的转录因子,可调节植物种子发育和ABA信号转导的关键方面。为了了解全球范围内VP1调控的基因表达,我们已经对在abi3无效突变体背景下携带35S :: VP1的转基因拟南芥进行了寡芯片分析。我们已经通过基因芯片分析鉴定了353个VP1 / ABA调控的基因。营养组织中VP1和ABA都影响了73%的基因,表明ABA信号传导与VP1功能之间紧密耦合。大量种子特异性基因在35S :: VP1植物的营养组织中异位表达,这与VP1和ABI3是种子特异性表达的关键决定因素的证据一致。 VP1激活了ABA信号的正向调节器ABI5,表明ABI3介导的前馈途径得以保守。 VP1强烈抑制ABA诱导ABA信号的负调节剂ABI1和ABI2,这揭示了前馈调节的第二条途径。这些结果表明,VP1通过ABI1 / ABI5相关基因的前馈调节强烈修饰ABA信号传导。在GeneChip上代表的32个bZIP转录因子中,ABI5进化枝中的基因被ABA和VP1特异性结合。对VP1 / ABA调控基因的5'上游序列进行的统计分析确定,共有的脱落反应元件为富集元件,表明许多基因可能是与ABI5相关的bZIPs的直接靶标。 Sph元件是由ABA和VP1共同激活的基因的启动子中富集的序列基序,而不是仅由ABA激活的基因的启动子中的富集序列基序。该分析揭示了启动子元件的独特组合模式区分了VP1 / ABA整合基因的亚类。

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