Knight Heather, Zarka Daniel G, Okamoto Haruko, Thomashow Michael F, Knight Marc R
Department of Plant Sciences, University of Oxford, Oxford, OX1 3RB, United Kingdom.
Plant Physiol. 2004 Jul;135(3):1710-7. doi: 10.1104/pp.104.043562. Epub 2004 Jul 9.
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.
拟南芥的许多冷调节基因可被脱落酸(ABA)以及低温诱导。人们认为这是通过两条独立的信号通路发生的,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。我们在此表明,ABA也能够激活CRT启动子元件。尽管最近发现的ABA诱导型CBF4转录因子可能对此有所解释,但我们在此表明,CBF1-3转录水平也会随着ABA水平升高而增加。CBF1-3转录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。CBF2启动子的总共125 bp,先前已证明足以用于冷、机械和环己酰亚胺诱导的表达,对于ABA诱导的表达也足够。然而,该区域内类似ABA响应启动子元件的基序对于ABA诱导的表达并非必需。ABA处理后观察到的CBF蛋白水平增加,以及先前的数据表明增加的CBF水平足以诱导冷调节基因,这表明ABA诱导的CBF1-3转录水平增加确实有可能激活CRT。因此,我们的数据表明,CRT的激活也可能通过一条新的ABA诱导信号通路发生,该通路使用通常由低温诱导的CBFs。