Pichon M, Journet E P, Dedieu A, de Billy F, Truchet G, Barker D G
Laboratoire de Biologie Moléculaire des Relations Plantes Microorganismes, INRA-CNRS, Castanet-Tolosan, France.
Plant Cell. 1992 Oct;4(10):1199-211. doi: 10.1105/tpc.4.10.1199.
To study the molecular responses of the host legume during early stages of the symbiotic interaction with Rhizobium, we have cloned and characterized the infection-related early nodulin gene MtENOD12 from Medicago truncatula. In situ hybridization experiments have shown that, within the indeterminate Medicago nodule, transcription of the MtENOD12 gene begins in cell layers of meristematic origin that lie ahead of the infection zone, suggesting that these cells are undergoing preparation for bacterial infection. Histochemical analysis of transgenic alfalfa plants that express an MtENOD12 promoter-beta-glucuronidase gene fusion has confirmed this result and further revealed that MtENOD12 gene transcription occurs as early as 3 to 6 hr following inoculation with R. meliloti in a zone of differentiating root epidermal cells which lies close to the growing root tip. It is likely that this transient, nodulation (nod) gene-dependent activation of the ENOD12 gene also corresponds to the preparation of the plant for bacterial infection. We anticipate that this extremely precocious response to Rhizobium will provide a valuable molecular marker for studying early signal exchange between the two symbiotic organisms.
为了研究宿主豆科植物在与根瘤菌共生相互作用早期阶段的分子反应,我们从蒺藜苜蓿中克隆并鉴定了与感染相关的早期结瘤素基因MtENOD12。原位杂交实验表明,在不定型的苜蓿根瘤中,MtENOD12基因的转录始于分生组织起源的细胞层,这些细胞层位于感染区之前,这表明这些细胞正在为细菌感染做准备。对表达MtENOD12启动子- β-葡萄糖醛酸酶基因融合体的转基因苜蓿植株进行的组织化学分析证实了这一结果,并进一步揭示,在靠近根尖生长部位的分化根表皮细胞区域,接种苜蓿中华根瘤菌后3至6小时,MtENOD12基因就开始转录。ENOD12基因这种短暂的、依赖结瘤(nod)基因的激活,可能也与植物为细菌感染所做的准备相对应。我们预计,这种对根瘤菌极其早熟的反应将为研究这两种共生生物之间的早期信号交换提供一个有价值的分子标记。