Boyce Thompson Institute for Plant Research, Ithaca, NY 14853-1801, USA.
Mol Plant Microbe Interact. 2010 Jun;23(6):715-26. doi: 10.1094/MPMI-23-6-0715.
In order to identify components of pathogen-associated molecular pattern-triggered immunity (PTI) pathways in Nicotiana benthamiana, we conducted a large-scale forward-genetics screen using virus-induced gene silencing and a cell-death-based assay for assessing PTI. The assay relied on four combinations of PTI-inducing nonpathogens and cell-death-causing challenger pathogens and was first validated in plants silenced for FLS2 or BAK1. Over 3,200 genes were screened and 14 genes were identified that, when silenced, compromised PTI as judged by the cell-death-based assay. Further analysis indicated that the 14 genes were not involved in a general cell death response. A subset of the genes was found to act downstream of FLS2-mediated PTI induction, and silencing of three genes compromised production of reactive oxygen species in leaves exposed to flg22. The 14 genes encode proteins with potential functions in defense and hormone signaling, protein stability and degradation, energy and secondary metabolism, and cell wall biosynthesis and provide a new resource to explore the molecular basis for the involvement of these processes in PTI.
为了鉴定烟草原生质体感受分子模式触发免疫(PTI)途径的组成成分,我们利用病毒诱导的基因沉默和基于细胞死亡的方法进行了大规模正向遗传学筛选,以评估 PTI。该方法依赖于四种 PTI 诱导非病原体和导致细胞死亡的挑战者病原体的组合,并且首先在沉默 FLS2 或 BAK1 的植物中进行了验证。筛选了超过 3200 个基因,并鉴定出 14 个基因,当这些基因沉默时,根据基于细胞死亡的测定,PTI 受到损害。进一步的分析表明,这 14 个基因不参与一般的细胞死亡反应。发现其中一组基因位于 FLS2 介导的 PTI 诱导的下游,并且沉默三个基因会损害暴露于 flg22 的叶片中活性氧的产生。这 14 个基因编码具有防御和激素信号转导、蛋白质稳定性和降解、能量和次生代谢以及细胞壁生物合成潜在功能的蛋白质,为探索这些过程参与 PTI 的分子基础提供了新的资源。