den Hartog M, Musgrave A, Munnik T
Swammerdam Institute for Life Sciences, Department of Plant Physiology, University of Amsterdam, Kruislaan 318, NL-1098 SM, Amsterdam, The Netherlands.
Plant J. 2001 Jan;25(1):55-65. doi: 10.1046/j.1365-313x.2001.00931.x.
Rhizobium-secreted nodulation factors are lipochitooligosaccharides that trigger the initiation of nodule formation on host legume roots. The first visible effect is root hair deformation, but the perception and signalling mechanisms that lead to this response are still unclear. When we treated Vicia sativa seedlings with mastoparan root hairs deformed, suggesting that G proteins are involved. To investigate whether mastoparan and Nod factor activate lipid signalling pathways initiated by phospholipase C (PLC) and D (PLD), seedlings were radiolabelled with [(32)P]orthophosphate prior to treatment. Mastoparan stimulated increases in phosphatidic acid (PA) and diacylglycerol pyrophosphate, indicative of PLD or PLC activity in combination with diacylglycerol kinase (DGK) and PA kinase. Treatment with Nod factor had similar effects, although less pronounced. The inactive mastoparan analogue Mas17 had no effect. The increase in PA was partially caused by the activation of PLD that was monitored by its in vivo transphosphatidylation activity. The application of primary butyl alcohols, inhibitors of PLD activity, blocked root hair deformation. Using different labelling strategies, evidence was provided for the activation of DGK. Since the PLC antagonist neomycin inhibited root hair deformation and the formation of PA, we propose that PLC activation produced diacylglycerol (DAG), which was subsequently converted to PA by DGK. The roles of PLC and PLD in Nod factor signalling are discussed.
根瘤菌分泌的结瘤因子是脂壳寡糖,可触发宿主豆科植物根上结瘤的形成。第一个可见的效应是根毛变形,但导致这种反应的感知和信号传导机制仍不清楚。当我们用 Mastoparan 处理蚕豆幼苗时,根毛发生变形,这表明 G 蛋白参与其中。为了研究 Mastoparan 和结瘤因子是否激活由磷脂酶 C(PLC)和 D(PLD)启动的脂质信号通路,在处理前用 [(32)P] 正磷酸盐对幼苗进行放射性标记。Mastoparan 刺激了磷脂酸(PA)和二酰基甘油焦磷酸的增加,这表明 PLD 或 PLC 活性与二酰基甘油激酶(DGK)和 PA 激酶相结合。用结瘤因子处理也有类似的效果,尽管不太明显。无活性的 Mastoparan 类似物 Mas17 没有效果。PA 的增加部分是由 PLD 的激活引起的,这通过其体内转磷脂酰化活性进行监测。PLD 活性抑制剂正丁醇的应用阻止了根毛变形。使用不同的标记策略,为 DGK 的激活提供了证据。由于 PLC 拮抗剂新霉素抑制了根毛变形和 PA 的形成,我们提出 PLC 的激活产生了二酰基甘油(DAG),随后 DAG 被 DGK 转化为 PA。文中讨论了 PLC 和 PLD 在结瘤因子信号传导中的作用。