Department of Plant Pathology, Physiology, and Weed Science, Virginia Tech, Blacksburg, VA 24060, USA.
Mol Plant Microbe Interact. 2010 Oct;23(10):1303-15. doi: 10.1094/MPMI-01-10-0022.
Plants disease resistance (R) genes encode specialized receptors that are quantitative, rate-limiting defense regulators. R genes must be expressed at optimum levels to function properly. If expression is too low, downstream defense responses are not activated efficiently. Conversely, overexpression of R genes can trigger autoactivation of defenses with deleterious consequences for the plant. Little is known about R gene regulation, particularly under defense-inducing conditions. We examined regulation of the Arabidopsis thaliana gene RPP8 (resistance to Hyaloperonospora arabidopsidis, isolate Emco5). RPP8 was induced in response to challenge with H. arabidopsidis or application of salicylic acid, as shown with RPP8-Luciferase transgenic plants and quantitative reverse-transcription polymerase chain reaction of endogenous alleles. The RPP1 and RPP4 genes were also induced by H. arabidopsidis and salicylic acid, suggesting that some RPP genes are subject to feedback amplification. The RPP8 promoter contains three W box cis elements. Site-directed mutagenesis of all three W boxes greatly diminished RPP8 basal expression, inducibility, and resistance in transgenic plants. Motif searches indicated that the W box is the only known cis element that is statistically overrepresented in Arabidopsis nucleotide-binding leucine-rich repeat promoters. These results indicate that WRKY transcription factors can regulate expression of surveillance genes at the top of the defense-signaling cascade.
植物疾病抗性 (R) 基因编码专门的受体,这些受体是定量的、限制防御反应的关键调节因子。R 基因必须在最佳水平表达才能正常发挥作用。如果表达水平过低,下游防御反应就不能有效地被激活。相反,R 基因的过度表达会触发防御的自动激活,对植物产生有害影响。关于 R 基因的调控,特别是在诱导防御的条件下,人们知之甚少。我们研究了拟南芥基因 RPP8(对 Hyaloperonospora arabidopsidis,Emco5 分离株的抗性)的调控。如 RPP8-Luciferase 转基因植物和内源性等位基因的定量反转录聚合酶链反应所示,RPP8 会响应 Hyaloperonospora arabidopsidis 的挑战或水杨酸的应用而被诱导。RPP1 和 RPP4 基因也被 Hyaloperonospora arabidopsidis 和水杨酸诱导,这表明一些 RPP 基因受到反馈放大的调控。RPP8 启动子包含三个 W 框顺式作用元件。对所有三个 W 框的定点突变极大地降低了转基因植物中 RPP8 的基础表达、诱导性和抗性。基序搜索表明,W 框是在拟南芥核苷酸结合亮氨酸丰富重复启动子中唯一被统计上过度代表的顺式元件。这些结果表明,WRKY 转录因子可以调节防御信号级联顶端的监测基因的表达。