Dissecting the WRKY Web of Plant Defense Regulators

During the past ten years, a large body of circumstantial evidence has accumulated, implicating WRKY factors in transcriptional reprogramming during plant immune responses [1–3]. Encoded by complex gene families in higher plants [4], these transcription factors share a DNA-binding domain (WRKY domain) comprising approximately 60 amino acids [5]. Additional conserved features of WRKYs are limited to separate subgroups of this family and include putative leucine zippers, nuclear localization signals, calmodulin binding sites, and several domains of unknown function [5–7]. Multiple studies have demonstrated the ability of WRKYs to bind to promoters of defense-associated genes via specific interactions of their WRKY domains with pathogen response elements termed W boxes (TTGACC/T) [8–11]. Both activating and repressing effects of WRKYs and W boxes on transcription have been observed [12–14]. It has also been shown that stable and transient overexpression of several WRKYs in the model plant Arabidopsis thaliana (Arabidopsis) conveys enhanced resistance to various bacterial or fungal pathogens [15–17]. The majority of the 74 Arabidopsis WRKY genes are transcriptionally inducible upon pathogen infection and other defense-related stimuli [18,19]. Interestingly, WRKY promoters are typically enriched for W boxes, thereby pointing to the existence of intricate regulatory circuits wherein functionally interconnected members of this family reside [19]. Indeed, multiple studies have revealed interactions of WRKYs with either their own promoters or those of other family members, suggesting that these transcription factors extensively engage in autoand crossregulation [9,12,13,20]. Such a WRKY web may ensure fast and efficient signal amplification. It may also allow for a tighter control in limiting the extent of defense responses via negative feedback mechanisms. A central component of the transcriptional network activated during immune responses in Arabidopsis is Nonexpresser of Pathogenesis-Related genes 1 (NPR1) [21]. This transcriptional cofactor is required for several different types of plant immune responses, including basal defense and systemic acquired resistance (SAR), which are dependent on the defense hormone salicylic acid (SA) [22]. Upon induction of basal defense or SAR, NPR1 is translocated from the cytosol to the nucleus where it mediates the binding of TGA basic leucine zipper protein transcription factors to their cognate promoter elements, resulting in the upregulation of a multitude of genes [23–28]. In addition, NPR1 is functionally linked to WRKYs during plant immune responses. Intriguingly, WRKYs control NPR1 expression on the one hand, while on the other hand seem to operate downstream from it [17,29,30]. Until now, the identity of WRKYs involved in NPR1-dependent signaling branches has for the most part remained a mystery. In contrast to WRKYs, NPR1 and TGA basic leucine zipper proteins are members of small families of only six and ten members in Arabidopsis, respectively. While mutant analyses have clearly proven the roles of NPR1 and several defined TGA basic leucine zipper proteins in pathogen defense [31– 33], such direct genetic evidence is scarce for WRKYs. With the exception of an atypical family member (AtWRKY52/ RRS1) [34], no WRKYs have been found to be involved in plant immune responses by mutant screens or other forward genetics approaches. In many cases, reverse genetics–based strategies to reveal biological roles of individual WRKYs using sequence-indexed Arabidopsis transferred DNA (T-DNA) or transposon insertion mutants have also proved to be unsuccessful in revealing defense-related phenotypes [2]. Functional redundancy among structurally related WRKY family members has been partially blamed for these experimental shortcomings [7]. In addition, in vivo roles of individual WRKYs may be limited to defined branches or nodes of the defense network. Hence, elimination of their function by mutation may result in quite specific or subtle phenotypes. Therefore, a major challenge in dissecting the WRKY web appears to be accurately pinpointing each WRKY’s sphere of activity prior to mutant analyses. This would narrow the choice of defense phenotypes to examine and may allow for the selection of appropriate candidates for double or higher-order mutant analyses. In a study published in this issue of PLoS Pathogens, Wang et al. succeeded in applying such a strategic approach [35]. A cleverly designed microarray experiment uncovered several WRKY genes that are direct transcriptional targets of NPR1. Wang and colleagues profiled transcriptome changes in transgenic Arabidopsis plants overexpressing an NPR1-GR (glucocorticoid receptor) fusion protein in an npr1 mutant background. Combined application of SA and the synthetic glucocorticoid dexamethasone activated the NPR1 pathway and triggered translocation of NPR1-GR to nuclei. By