Groupe Rhizogenèse, Unité Mixte de Recherche Diversité et Adaptation des Plantes Cultivées, Institut de Recherche pour le Développement, 911 avenue Agropolis, BP 5045, 34394 Montpellier Cedex 5, France.
Mol Plant Microbe Interact. 2010 Jun;23(6):740-7. doi: 10.1094/MPMI-23-6-0740.
The MtEnod11 gene from Medicago truncatula is widely used as an early infection-related molecular marker for endosymbiotic associations involving both rhizobia and arbuscular mycorrhizal fungi. In this article, heterologous expression of the MtEnod11 promoter has been studied in two actinorhizal trees, Casuarina glauca and Allocasuarina verticillata. Transgenic C. glauca and A. verticillata expressing a ProMtEnod11::beta-glucuronidase (gus) fusion were generated and the activation of the transgene investigated in the context of the symbiotic associations with the N-fixing actinomycete Frankia and both endo- and ectomycorrhizal fungi (Glomus intraradices and Pisolithus albus, respectively). ProMtEnod11::gus expression was observed in root hairs, prenodules, and nodules and could be correlated with the infection of plant cells by Frankia spp. However, no activation of the gus reporter gene was detected prior to infection or in response to either rhizobial Nod factors or the wasp venom peptide MAS-7. Equally, ProMtEnod11::gus expression was not elicited during the symbiotic associations with either ecto- or endomycorrhizal fungi. These observations suggest that, although there is a conservation of gene regulatory pathways between legumes and actinorhizal plants in cells accommodating endosymbiotic N-fixing bacteria, the events preceding bacterial infection or related to mycorrhization appear to be less conserved.
来自紫花苜蓿的 MtEnod11 基因被广泛用作涉及根瘤菌和丛枝菌根真菌的共生相关的早期感染相关分子标记。在本文中,研究了拟南芥和垂柏两种放线菌根树中 MtEnod11 启动子的异源表达。生成了表达 ProMtEnod11::β-葡萄糖醛酸酶(gus)融合蛋白的转基因 C. glauca 和 A. verticillata,并在与固氮放线菌 Frankia 以及内、外生菌根真菌(Glomus intraradices 和 Pisolithus albus)共生关联的背景下研究了转基因的激活。在根毛、预结瘤和根瘤中观察到 ProMtEnod11::gus 的表达,并且可以与 Frankia spp. 感染植物细胞相关联。然而,在感染之前或对根瘤菌 Nod 因子或黄蜂毒液肽 MAS-7 的响应中,均未检测到 gus 报告基因的激活。同样,在与外生菌根或内生菌根真菌的共生关联中,ProMtEnod11::gus 的表达也未被激发。这些观察结果表明,尽管在容纳共生固氮细菌的细胞中,豆科植物和放线菌根植物之间存在基因调控途径的保守性,但在细菌感染之前或与菌根化相关的事件似乎不太保守。