PP2C 磷酸酶 Pic6 可抑制 MAPK 激活和番茄的抗病性。

IF 3.2 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Molecular Plant-microbe Interactions Pub Date : 2024-11-16 DOI:10.1094/MPMI-10-24-0124-SC
Joydeep Chakraborty, Guy Sobol, Fan Xia, Ning Zhang, Gregory B Martin, Guido Sessa
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引用次数: 0

摘要

2C 型蛋白磷酸酶(PP2Cs)对于调节植物对病原体的免疫反应至关重要。我们的研究侧重于番茄 PP2C 免疫相关候选 6(Pic6),阐明其在负向调节番茄模式触发免疫(PTI)信号通路中的作用。利用反转录定量聚合酶链式反应(RT-qPCR),我们观察到用微生物相关分子模式(MAMPs)--flg22 和 flgII-28 处理野生型(RG-PtoR)番茄植株后,Pic6 mRNA 水平显著增加。Pic6 具有一个保守的 N 端激酶相互作用基序(KIM)和一个 C 端 PP2C 结构域。我们制备了这些区域发生突变的 Pic6 变体,证明它们参与了番茄免疫的负向调控。与 YFP 对照相比,农杆菌介导的 Pic6 瞬时过表达导致细菌病原体 Pseudomonas syringae pv. tomato(Pst)菌株 DC3000ΔhopQ1-1 的生长增强。此外,Pic6 的过表达抑制了丝裂原活化蛋白激酶(MAPK)对 flg22 和 flgII-28 处理的激活。重要的是,Pic6 具有磷酸酶活性,能与番茄 Mkk1/Mkk2 蛋白相互作用,并以 KIM 依赖性方式使其去磷酸化。此外,我们还通过 CRISPR/Cas9 生成了 RG-pic6 功能缺失突变体,结果表明,与野生型(RG-PtoR)植株相比,Pic6 的缺失提高了 MAPK 活性,增强了对黄单胞菌菌株 85-10 (Xe 85-10)的抗性。转录本分析表明,与野生型(RG-PtoR)植物相比,经 flg22/flgII-28 处理后,RG-pic6 突变体中的 PTI 报告基因 NAC 和 osmotin 明显上调。总之,我们的研究结果表明,Pic6 是 MAPK 信号转导的负调控因子,在调节番茄对细菌病原体的免疫力方面起着关键作用。
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PP2C phosphatase Pic6 suppresses MAPK activation and disease resistance in tomato.

Type 2C protein phosphatases (PP2Cs) are essential for regulating plant immune responses to pathogens. Our study focuses on the tomato PP2C-immunity associated candidate 6 (Pic6), elucidating its role in negatively regulating pattern-triggered immunity (PTI) signaling pathways in tomato. Using reverse transcription quantitative polymerase chain reaction (RT-qPCR), we observed that treatment with microbe-associated molecular patterns (MAMPs)- flg22 and flgII-28-significantly increased Pic6 mRNA levels in wild-type (RG-PtoR) tomato plants. Pic6 features a conserved N-terminal kinase-interacting motif (KIM) and a C-terminal PP2C domain. We produced variants of Pic6 with mutations in these regions, demonstrating their involvements in negatively regulating tomato immunity. Agrobacterium-mediated transient overexpression of Pic6 resulted in enhanced growth of the bacterial pathogen Pseudomonas syringae pv. tomato (Pst) strain DC3000ΔhopQ1-1 compared to a YFP control. Additionally, Pic6 overexpression inhibited mitogen-activated protein kinase (MAPK) activation in response to flg22 and flgII-28 treatments. Importantly, Pic6 exhibited phosphatase activity and interacted with tomato Mkk1/Mkk2 proteins and dephosphorylated them in a KIM-dependent manner. Furthermore, we generated RG-pic6 loss-of-function mutants by CRISPR/Cas9, revealing that the absence of Pic6 heightened MAPK activity and increased resistance to Xanthomonas euvesicatoria strain 85-10 (Xe 85-10) when compared with the wild-type (RG-PtoR) plants. Transcript analyses showed that after flg22/flgII-28 treatment, PTI-reporter genes NAC and osmotin were significantly upregulated in RG-pic6 mutants in comparison to the wild-type (RG-PtoR) plants. Overall, our findings indicate that Pic6 acts as a negative regulator of MAPK signaling and playing a pivotal role in modulating tomato immunity against bacterial pathogens.

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来源期刊
Molecular Plant-microbe Interactions
Molecular Plant-microbe Interactions 生物-生化与分子生物学
CiteScore
7.00
自引率
2.90%
发文量
250
审稿时长
3 months
期刊介绍: Molecular Plant-Microbe Interactions® (MPMI) publishes fundamental and advanced applied research on the genetics, genomics, molecular biology, biochemistry, and biophysics of pathological, symbiotic, and associative interactions of microbes, insects, nematodes, or parasitic plants with plants.
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