Journet E P, Pichon M, Dedieu A, de Billy F, Truchet G, Barker D G
Laboratoire de Biologie Moléculaire des Relations Plantes-Microorganismes, INRA-CNRS, Castanet-Tolosan, France.
Plant J. 1994 Aug;6(2):241-9. doi: 10.1046/j.1365-313x.1994.6020241.x.
Extracellular lipo-oligosaccharides of Rhizobium, known as Nod factors, play a key role in the molecular signal exchange which leads to the specific nitrogen-fixing symbiotic association between the soil microbe and its host legume. The biological activity of Nod factors and their perception by the host plant during the earliest stages of the Rhizobium/legume interaction have been studied using transgenic alfalfa carrying a fusion between the promoter of the early nodulin gene MtENOD12 and the beta-glucuronidase (GUS) reporter gene. Histochemical staining has shown that GUS accumulates specifically in the differentiating root epidermis, prior to and during root hair emergence, within 2-3 h following the addition of purified Rhizobium meliloti Nod factors. This precocious transcriptional activation of the MtENOD12 gene, reminiscent of that observed after inoculation with intact Rhizobium, implies that the Nod factor signal can be perceived at a developmental stage preceding root hair formation. GUS activity can be detected following treatment with a wide range of R. meliloti Nod factor concentrations down to 10(-13) M, and furthermore, this rapid response to the bacterial elicitor appears to be non-systemic. Significantly, MtENOD12-GUS expression is not observed after inoculation with a R. meliloti nodH mutant which synthesizes exclusively non-sulphated Nod factors. Indeed purified Nod factors which lack the sulphate substituent are approximately 1000-fold less active than their sulphated counterparts. Thus, the triggering of ENOD12 transcription in the alfalfa root epidermis is a rapid molecular response which is subject to the same host-specificity determinant (Nod factor sulphation) that governs the interaction between alfalfa and its bacterial symbiont.
根瘤菌的细胞外脂寡糖,即结瘤因子,在分子信号交换中起关键作用,这种信号交换导致土壤微生物与其宿主豆科植物之间形成特定的固氮共生关系。利用携带早期结瘤素基因MtENOD12启动子与β-葡萄糖醛酸酶(GUS)报告基因融合体的转基因苜蓿,研究了结瘤因子的生物活性及其在根瘤菌/豆科植物相互作用最早阶段被宿主植物感知的情况。组织化学染色表明,在添加纯化的苜蓿根瘤菌结瘤因子后2 - 3小时内,根毛出现之前及出现过程中,GUS特异性地积累在分化的根表皮中。MtENOD12基因的这种早熟转录激活,类似于接种完整根瘤菌后观察到的情况,这意味着结瘤因子信号可以在根毛形成之前的发育阶段被感知。用低至10^(-13) M的多种苜蓿根瘤菌结瘤因子浓度处理后均可检测到GUS活性,此外,对细菌激发子的这种快速反应似乎不是系统性的。值得注意的是,接种仅合成非硫酸化结瘤因子的苜蓿根瘤菌nodH突变体后未观察到MtENOD12 - GUS表达。实际上,缺乏硫酸盐取代基的纯化结瘤因子的活性比其硫酸化对应物低约1000倍。因此,苜蓿根表皮中ENOD12转录的触发是一种快速的分子反应,它受制于控制苜蓿与其细菌共生体相互作用的相同宿主特异性决定因素(结瘤因子硫酸化)。