Nod factor-induced phosphatidic acid and diacylglycerol pyrophosphate formation: a role for phospholipase C and D in root hair deformation.

M. D. Hartog, A. Musgrave, T. Munnik
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引用次数: 178

Abstract

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.
节点因子诱导的磷脂酸和焦磷酸二酰基甘油形成:磷脂酶C和D在根毛变形中的作用。
根瘤菌分泌的结瘤因子是一种脂壳寡糖,它能触发寄主豆科植物根部的结瘤形成。第一个可见的影响是根毛变形,但导致这种反应的感知和信号机制尚不清楚。当我们处理蚕豆幼苗时,乳突根毛发生变形,表明G蛋白参与其中。为了研究mastoparan和Nod因子是否激活磷脂酶C (PLC)和D (PLD)启动的脂质信号通路,在处理前用正磷酸盐[(32)P]对幼苗进行放射性标记。Mastoparan刺激磷脂酸(PA)和焦磷酸二酰基甘油增加,表明PLD或PLC活性与二酰基甘油激酶(DGK)和PA激酶联合。用Nod因子治疗也有类似的效果,尽管不那么明显。失活的乳腺炎类似物Mas17没有作用。PA的增加部分是由PLD的激活引起的,PLD的激活是通过其体内转磷脂酰化活性来监测的。应用伯丁醇,抑制PLD活性,阻断根毛变形。使用不同的标记策略,为DGK的激活提供了证据。由于PLC拮抗剂新霉素抑制根毛变形和PA的形成,我们提出PLC激活产生二酰基甘油(DAG),随后由DGK转化为PA。讨论了PLC和PLD在节点信号中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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