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Abscisic Acid Induces CBF Gene Transcription and Subsequent Induction of Cold-Regulated Genes via the CRT Promoter Element

机译:脱落酸通过CRT启动子元件诱导CBF基因转录并​​随后诱导冷调节基因

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摘要

Many cold-regulated genes of Arabidopsis are inducible by abscisic acid (ABA) as well as by cold. This has been thought to occur via two separate signaling pathways, with ABA acting via ABA-responsive promoter elements and low temperature activating the C-repeat element (CRT; dehydration-responsive) promoter element via CBF (DREB1) transcription factors. We show here that ABA is also capable of activating the CRT promoter element. Although the more recently discovered ABA-inducible CBF4 transcription factor might have accounted for this, we show here that CBF1-3 transcript levels also increase in response to elevated ABA levels. This increase in CBF1-3 transcript levels appears to be at least in part due to increased activity of the CBF promoters in response to ABA. A total of 125 bp of the CBF2 promoter, which has previously been shown to be sufficient for cold-, mechanical-, and cycloheximide-induced expression, was also sufficient for ABA-induced expression. However, the ABA-responsive promoter element-like motif within this region is not needed for ABA-induced expression. An observed increase in CBF protein levels after ABA treatment, together with previous data showing that increased CBF levels are sufficient for cold-regulated gene induction, suggests that ABA-induced increases in CBF1-3 transcript levels do have the potential to activate the CRT. Our data indicate therefore that activation of the CRT may also occur via a novel ABA-inducible signaling pathway using the normally cold-inducible CBFs.
机译:脱落酸(ABA)和感冒均可诱导拟南芥的许多冷调节基因。人们认为这是通过两个单独的信号传导途径发生的,ABA通过ABA响应启动子元件起作用,而低温则通过CBF(DREB1)转录因子激活C重复元件(CRT;脱水响应)启动子元件。我们在这里显示ABA也能够激活CRT启动子元件。尽管最近发现的ABA诱导型CBF4转录因子可能是造成这种现象的原因,但我们在这里表明CBF1-3转录水平也随着ABA水平的升高而增加。 CBF1-3转录物水平的这种增加似乎至少部分是由于CBF启动子响应ABA的活性增加。总共已显示125 bp的CBF2启动子(以前已证明足以用于冷,机械和环己酰亚胺诱导的表达),也足以用于ABA诱导的表达。然而,ABA诱导的表达不需要该区域内的ABA响应性启动子元件样基序。 ABA处理后观察到的CBF蛋白水平升高,以及先前的数据表明CBF水平升高足以冷调节基因诱导,这表明ABA诱导的CBF1-3转录水平升高确实具有激活CRT的潜力。因此,我们的数据表明,CRT的激活也可能通过使用通常可冷诱导的CBF通过新的ABA诱导的信号传导途径发生。

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