Boyce Thompson Institute for Plant Research, Ithaca, New York 14853, USA.
Plant Cell. 2010 Jan;22(1):260-72. doi: 10.1105/tpc.109.070664. Epub 2010 Jan 8.
Programmed cell death (PCD) is triggered when Pto, a Ser-Thr protein kinase, recognizes either the AvrPto or AvrPtoB effector from Pseudomonas syringae pv tomato. This PCD requires mitogen-activated protein kinase kinase kinase (MAPKKK alpha ) as a positive regulator in tomato (Solanum lycopersicum) and Nicotiana benthamiana. To examine how PCD-eliciting activity of the tomato MAPKKK alpha protein is regulated, we screened for MAPKKK alpha -interacting proteins in tomato and identified a 14-3-3 protein, TFT7. Virus-induced gene silencing using the TFT7 gene in N. benthamiana compromised both Pto- and MAPKKK alpha -mediated PCD, and coexpression of TFT7 with tomato MAPKKK alpha enhanced MAPKKK alpha -mediated PCD. TFT7 was also required for PCD associated with several other disease resistance proteins and contributed to resistance against P. syringae pv tomato. Coexpression of TFT7 with MAPKKK alpha in vivo caused increased accumulation of the kinase and enhanced phosphorylation of two MAP kinases. TFT7 protein contains a phosphopeptide binding motif that is present in human 14-3-3 epsilon, and substitutions in this motif abolished interaction with MAPKKK alpha in vivo and also the PCD-enhancing activity of TFT7. A 14-3-3 binding motif, including a putative phosphorylated Ser-535, is present in the C-terminal region of MAPKKK alpha. An S535A substitution in MAPKKK alpha reduced interaction with TFT7 and both PCD-eliciting ability and stability of MAPKKK alpha. Our results provide new insights into a role for 14-3-3 proteins in regulating immunity-associated PCD pathways in plants.
程序性细胞死亡 (PCD) 是由 Pto 蛋白激酶识别丁香假单胞菌 pv 番茄中的 AvrPto 或 AvrPtoB 效应子时触发的。这种 PCD 需要丝裂原活化蛋白激酶激酶激酶 (MAPKKKα) 作为番茄 (Solanum lycopersicum) 和烟草 (Nicotiana benthamiana) 的正向调节剂。为了研究番茄 MAPKKKα 蛋白引发 PCD 的活性是如何被调节的,我们在番茄中筛选了 MAPKKKα 相互作用蛋白,并鉴定出一种 14-3-3 蛋白 TFT7。在烟草中利用 TFT7 基因进行病毒诱导的基因沉默,削弱了 Pto 和 MAPKKKα 介导的 PCD,并且与番茄 MAPKKKα 共表达增强了 MAPKKKα 介导的 PCD。TFT7 也与几种其他抗病蛋白相关的 PCD 有关,并有助于对丁香假单胞菌 pv 番茄的抗性。在体内与 MAPKKKα 共表达 TFT7 导致激酶的积累增加,并增强了两种 MAP 激酶的磷酸化。TFT7 蛋白含有一个磷酸肽结合基序,存在于人 14-3-3ε 中,该基序中的取代在体内消除了与 MAPKKKα 的相互作用,也消除了 TFT7 的 PCD 增强活性。MAPKKKα 的 C 末端区域存在一个 14-3-3 结合基序,包括一个假定的磷酸化 Ser-535。MAPKKKα 中的 S535A 取代降低了与 TFT7 的相互作用,以及 PCD 引发能力和 MAPKKKα 的稳定性。我们的研究结果为 14-3-3 蛋白在调节植物中与免疫相关的 PCD 途径方面提供了新的见解。