Canella Donatella, Gilmour Sarah J, Kuhn Leslie A, Thomashow Michael F
Michigan State University, East Lansing, MI 48824, USA.
Biochim Biophys Acta. 2010 May-Jun;1799(5-6):454-62. doi: 10.1016/j.bbagrm.2009.11.017. Epub 2009 Nov 27.
The CBF/DREB1 transcriptional activators are key regulators of plant freezing tolerance. They are members of the AP2/ERF multi-gene family, which in Arabidopsis comprises about 145 members. Common to these proteins is the AP2/ERF DNA-binding domain, a 60-amino-acid fold composed of a three-stranded beta-sheet followed by a C-terminal alpha-helix. A feature that distinguishes the CBF proteins from the other AP2/ERF proteins is the presence of "signature sequences," PKKP/RAGRxKFxETRHP (abbreviated PKKPAGR) and DSAWR, which are located immediately upstream and downstream, respectively, of the AP2/ERF DNA-binding domain. The signature sequences are highly conserved in CBF proteins from diverse plant species suggesting that they have an important functional role. Here we show that the PKKPAGR sequence of AtCBF1 is essential for its transcriptional activity. Deletion of the sequence or mutations within it greatly impaired the ability of CBF1 to induce expression of its target genes. This impairment was not due to the mutations eliminating CBF1 localization to the nucleus or preventing protein accumulation. Rather, we show that this loss of function was due to the mutations greatly impairing the ability of the CBF1 protein to bind to its DNA recognition sequence, the CRT/DRE element. These results establish that the ability of the CBF proteins to bind to the CRT/DRE element requires amino acids that extend beyond the AP2/ERF DNA-binding domain and raise the possibility that the PKKPAGR sequence contributes to determining the DNA-binding specificity of the CBF proteins.
CBF/DREB1转录激活因子是植物抗冻性的关键调节因子。它们是AP2/ERF多基因家族的成员,在拟南芥中该家族约有145个成员。这些蛋白质的共同特征是AP2/ERF DNA结合结构域,这是一个由三条链的β折叠组成,后面跟着一个C端α螺旋的60个氨基酸的折叠结构。CBF蛋白与其他AP2/ERF蛋白的一个区别特征是存在“特征序列”,即PKKP/RAGRxKFxETRHP(缩写为PKKPAGR)和DSAWR,它们分别位于AP2/ERF DNA结合结构域的紧邻上游和下游。这些特征序列在来自不同植物物种的CBF蛋白中高度保守,表明它们具有重要的功能作用。在这里,我们表明AtCBF1的PKKPAGR序列对其转录活性至关重要。该序列的缺失或其中的突变极大地损害了CBF1诱导其靶基因表达的能力。这种损害不是由于突变消除了CBF1在细胞核中的定位或阻止了蛋白质积累。相反,我们表明这种功能丧失是由于突变极大地损害了CBF1蛋白与其DNA识别序列CRT/DRE元件结合的能力。这些结果表明,CBF蛋白与CRT/DRE元件结合的能力需要超出AP2/ERF DNA结合结构域的氨基酸,并增加了PKKPAGR序列有助于确定CBF蛋白DNA结合特异性的可能性。