Ciolkowski Ingo, Wanke Dierk, Birkenbihl Rainer P, Somssich Imre E
Department of Plant Microbe Interactions, Max Planck Institute for Plant Breeding Research, Carl-von-Linné-Weg 10, Koln, Germany.
Plant Mol Biol. 2008 Sep;68(1-2):81-92. doi: 10.1007/s11103-008-9353-1. Epub 2008 Jun 4.
WRKY transcription factors have been shown to play a major role in regulating, both positively and negatively, the plant defense transcriptome. Nearly all studied WRKY factors appear to have a stereotypic binding preference to one DNA element termed the W-box. How specificity for certain promoters is accomplished therefore remains completely unknown. In this study, we tested five distinct Arabidopsis WRKY transcription factor subfamily members for their DNA binding selectivity towards variants of the W-box embedded in neighboring DNA sequences. These studies revealed for the first time differences in their binding site preferences, which are partly dependent on additional adjacent DNA sequences outside of the TTGACY-core motif. A consensus WRKY binding site derived from these studies was used for in silico analysis to identify potential target genes within the Arabidopsis genome. Furthermore, we show that even subtle amino acid substitutions within the DNA binding region of AtWRKY11 strongly impinge on its binding activity. Additionally, all five factors were found localized exclusively to the plant cell nucleus and to be capable of trans-activating expression of a reporter gene construct in vivo.
WRKY转录因子已被证明在正向和负向调控植物防御转录组中发挥主要作用。几乎所有已研究的WRKY因子似乎对一种称为W-box的DNA元件具有刻板的结合偏好。因此,某些启动子的特异性是如何实现的仍然完全未知。在本研究中,我们测试了五个不同的拟南芥WRKY转录因子亚家族成员对嵌入相邻DNA序列中的W-box变体的DNA结合选择性。这些研究首次揭示了它们结合位点偏好的差异,这部分取决于TTGACY核心基序之外的额外相邻DNA序列。从这些研究中得出的WRKY结合位点共识用于计算机分析,以鉴定拟南芥基因组中的潜在靶基因。此外,我们表明,即使AtWRKY11的DNA结合区域内的细微氨基酸取代也会强烈影响其结合活性。此外,发现所有五个因子都仅定位于植物细胞核,并且能够在体内反式激活报告基因构建体的表达。