首页> 美国卫生研究院文献>The Plant Cell >A MPK3/6-WRKY33-ALD1-Pipecolic Acid Regulatory Loop Contributes to Systemic Acquired Resistance
【2h】

A MPK3/6-WRKY33-ALD1-Pipecolic Acid Regulatory Loop Contributes to Systemic Acquired Resistance

机译:MPK3 / 6-WRKY33-ALD1-哌酸调节环有助于系统获得性耐药

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Plants induce systemic acquired resistance (SAR) upon localized exposure to pathogens. Pipecolic acid (Pip) production via AGD2-LIKE DEFENSE RESPONSE PROTEIN1 (ALD1) is key for SAR establishment. Here, we report a positive feedback loop important for SAR induction in Arabidopsis thaliana. We showed that local activation of the MAP kinases MPK3 and MPK6 is sufficient to trigger Pip production and mount SAR. Consistent with this, mutations in MPK3 or MPK6 led to compromised Pip accumulation upon inoculation with the bacterial pathogen Pseudomonas syringae pv tomato DC3000 (Pto) AvrRpt2, which triggers strong sustained MAPK activation. By contrast, P. syringae pv maculicola and Pto, which induce transient MAPK activation, trigger Pip biosynthesis and SAR independently of MPK3/6. ALD1 expression, Pip accumulation, and SAR were compromised in mutants defective in the MPK3/6-regulated transcription factor WRKY33. Chromatin immunoprecipitation showed that WRKY33 binds to the ALD1 promoter. We found that Pip triggers activation of MPK3 and MPK6 and that MAPK activation after Pto AvrRpt2 inoculation is compromised in wrky33 and ald1 mutants. Collectively, our results reveal a positive regulatory loop consisting of MPK3/MPK6, WRKY33, ALD1, and Pip in SAR induction and suggest the existence of distinct SAR activation pathways that converge at the level of Pip biosynthesis.
机译:植物在局部暴露于病原体时会诱导系统获得性抗性(SAR)。通过AGD2-Like防御反应蛋白1(ALD1)生产的胡椒酸(Pip)是建立SAR的关键。在这里,我们报告了一个积极的反馈回路,对于拟南芥中的SAR诱导很重要。我们表明,MAP激酶MPK3和MPK6的局部激活足以触发Pip产生并安装SAR。与此一致的是,接种细菌性病原体丁香假单胞菌pv番茄DC3000(Pto)AvrRpt2时,MPK3或MPK6突变导致受损的Pip积累受损,从而触发了强烈的持续MAPK激活。相比之下,丁香假单胞菌pv maculicola和Pto诱导瞬时MAPK活化,独立于MPK3 / 6触发Pip生物合成和SAR。在MPK3 / 6调控的转录因子WRKY33中存在缺陷的突变体中,ALD1表达,Pip积累和SAR受到损害。染色质免疫沉淀显示WRKY33与ALD1启动子结合。我们发现Pip触发了MPK3和MPK6的激活,并且在wrky33和ald1突变体中,Pto AvrRpt2接种后MAPK激活受到损害。总的来说,我们的研究结果揭示了在SAR诱导中由MPK3 / MPK6,WRKY33,ALD1和Pip组成的正向调节回路,并暗示了在Pip生物合成水平上会聚的独特SAR激活途径的存在。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号