Department of Forest Genetics and Plant Physiology, Umeå Plant Science Center, Swedish University of Agricultural Sciences, 90183, Umeå, Sweden.
Department of Plant Physiology, Umeå Plant Science Center, Umeå University, 90187, Umeå, Sweden.
New Phytol. 2022 Oct;236(2):639-655. doi: 10.1111/nph.18358. Epub 2022 Jul 27.
The development of ectomycorrhizal (ECM) symbioses between soil fungi and tree roots requires modification of root cell walls. The pectin-mediated adhesion between adjacent root cells loosens to accommodate fungal hyphae in the Hartig net, facilitating nutrient exchange between partners. We investigated the role of fungal pectin modifying enzymes in Laccaria bicolor for ECM formation with Populus tremula × Populus tremuloides. We combine transcriptomics of cell-wall-related enzymes in both partners during ECM formation, immunolocalisation of pectin (Homogalacturonan, HG) epitopes in different methylesterification states, pectin methylesterase (PME) activity assays and functional analyses of transgenic L. bicolor to uncover pectin modification mechanisms and the requirement of fungal pectin methylesterases (LbPMEs) for ECM formation. Immunolocalisation identified remodelling of pectin towards de-esterified HG during ECM formation, which was accompanied by increased LbPME1 expression and PME activity. Overexpression or RNAi of the ECM-induced LbPME1 in transgenic L. bicolor lines led to reduced ECM formation. Hartig Nets formed with LbPME1 RNAi lines were shallower, whereas those formed with LbPME1 overexpressors were deeper. This suggests that LbPME1 plays a role in ECM formation potentially through HG de-esterification, which initiates loosening of adjacent root cells to facilitate Hartig net formation.
外生菌根(ECM)共生体是土壤真菌和植物根系之间的共生关系,其形成需要对根系细胞壁进行修饰。果胶介导的相邻根系细胞间的黏附作用会松弛,以容纳哈蒂网中的真菌菌丝,从而促进伙伴之间的养分交换。我们研究了土壤真菌果胶修饰酶在 Laccaria bicolor 与 Populus tremula × Populus tremuloides 形成 ECM 中的作用。我们结合了细胞壁相关酶在 ECM 形成过程中的转录组学、不同甲酯化状态下果胶(半乳糖醛酸聚糖,HG)表位的免疫定位、果胶甲酯酶(PME)活性测定以及 L. bicolor 的转基因功能分析,以揭示果胶修饰机制和真菌果胶甲酯酶(LbPMEs)对 ECM 形成的需求。免疫定位鉴定了 ECM 形成过程中果胶向去酯化 HG 的重塑,这伴随着 LbPME1 表达和 PME 活性的增加。在转基因 L. bicolor 系中过表达或 RNAi 处理 ECM 诱导的 LbPME1,导致 ECM 形成减少。用 LbPME1 RNAi 系形成的哈蒂网较浅,而用 LbPME1 过表达系形成的哈蒂网较深。这表明 LbPME1 通过 HG 去酯化在 ECM 形成中发挥作用,这可能导致相邻根系细胞的松弛,从而促进哈蒂网的形成。