Department of Plant-Microbe Interactions, Max-Planck Institute for Plant Breeding Research Cologne, Germany.
Front Plant Sci. 2013 Oct 17;4:403. doi: 10.3389/fpls.2013.00403. eCollection 2013.
In plant effector-triggered immunity (ETI), intracellular nucleotide binding-leucine rich repeat (NLR) receptors are activated by specific pathogen effectors. The Arabidopsis TIR (Toll-Interleukin-1 receptor domain)-NLR (denoted TNL) gene pair, RPS4 and RRS1, confers resistance to Pseudomonas syringae pv tomato (Pst) strain DC3000 expressing the Type III-secreted effector, AvrRps4. Nuclear accumulation of AvrRps4, RPS4, and the TNL resistance regulator EDS1 is necessary for ETI. RRS1 possesses a C-terminal "WRKY" transcription factor DNA binding domain suggesting that important RPS4/RRS1 recognition and/or resistance signaling events occur at the nuclear chromatin. In Arabidopsis accession Ws-0, the RPS4(Ws) /RRS1(Ws) allelic pair governs resistance to Pst/AvrRps4 accompanied by host programed cell death (pcd). In accession Col-0, RPS4(Col) /RRS1(Col) effectively limits Pst/AvrRps4 growth without pcd. Constitutive expression of HA-StrepII tagged RPS4(Col) (in a 35S:RPS4-HS line) confers temperature-conditioned EDS1-dependent auto-immunity. Here we show that a high (28°C, non-permissive) to moderate (19°C, permissive) temperature shift of 35S:RPS4-HS plants can be used to follow defense-related transcriptional dynamics without a pathogen effector trigger. By comparing responses of 35S:RPS4-HS with 35S:RPS4-HS rrs1-11 and 35S:RPS4-HS eds1-2 mutants, we establish that RPS4(Col) auto-immunity depends entirely on EDS1 and partially on RRS1(Col) . Examination of gene expression microarray data over 24 h after temperature shift reveals a mainly quantitative RRS1(Col) contribution to up- or down-regulation of a small subset of RPS4(Col) -reprogramed, EDS1-dependent genes. We find significant over-representation of WRKY transcription factor binding W-box cis-elements within the promoters of these genes. Our data show that RRS1(Col) contributes to temperature-conditioned RPS4(Col) auto-immunity and are consistent with activated RPS4(Col) engaging RRS1(Col) for resistance signaling.
在植物效应物触发的免疫(ETI)中,细胞内核苷酸结合亮氨酸丰富重复(NLR)受体被特定的病原体效应物激活。拟南芥 TIR(Toll-Interleukin-1 受体结构域)-NLR(表示为 TNL)基因对 RPS4 和 RRS1 赋予了对表达 III 型分泌效应物 AvrRps4 的丁香假单胞菌 pv 番茄(Pst)菌株 DC3000 的抗性。AvrRps4、RPS4 和 TNL 抗性调节剂 EDS1 的核积累对于 ETI 是必要的。RRS1 具有 C 末端“WRKY”转录因子 DNA 结合结构域,这表明在核染色质上发生了重要的 RPS4/RRS1 识别和/或抗性信号事件。在拟南芥品种 Ws-0 中,RPS4(Ws)/RRS1(Ws)等位基因对 Pst/AvrRps4 具有抗性,同时伴有宿主程序性细胞死亡(pcd)。在品种 Col-0 中,RPS4(Col)/RRS1(Col)有效地限制了 Pst/AvrRps4 的生长而没有 pcd。HA-StrepII 标记的 RPS4(Col)(在 35S:RPS4-HS 系中)的组成型表达赋予了温度条件依赖性的 EDS1 依赖性自身免疫。在这里,我们表明,35S:RPS4-HS 植物的高(28°C,非许可)到中等(19°C,许可)温度变化可以用于在没有病原体效应物触发的情况下跟踪与防御相关的转录动态。通过比较 35S:RPS4-HS 与 35S:RPS4-HS rrs1-11 和 35S:RPS4-HS eds1-2 突变体的反应,我们确定了 RPS4(Col)自身免疫完全依赖于 EDS1,部分依赖于 RRS1(Col)。对温度变化后 24 小时的基因表达微阵列数据的检查揭示了 RRS1(Col)主要在数量上对一小部分 RPS4(Col)-重编程、EDS1 依赖性基因的上调或下调有贡献。我们发现这些基因启动子内 WRKY 转录因子结合 W 盒顺式元件的显著过表达。我们的数据表明,RRS1(Col)有助于温度条件下的 RPS4(Col)自身免疫,并且与激活的 RPS4(Col)用于抗性信号的情况一致。