Tamayo Elisabeth, Figueira-Galán David, Manck-Götzenberger Jasmin, Requena Natalia
Molecular Phytopathology, Botanical Institute, Karlsruhe Institute of Technology (KIT), Karlsruhe, Germany.
Front Plant Sci. 2022 Mar 24;13:837231. doi: 10.3389/fpls.2022.837231. eCollection 2022.
Root colonization by filamentous fungi modifies sugar partitioning in plants by increasing the sink strength. As a result, a transcriptional reprogramming of sugar transporters takes place. Here we have further advanced in the characterization of the potato SWEET sugar transporters and their regulation in response to the colonization by symbiotic and pathogenic fungi. We previously showed that root colonization by the AM fungus induces a major transcriptional reprogramming of the 35 potato SWEETs, with 12 genes induced and 10 repressed. In contrast, here we show that during the early colonization phase, the necrotrophic fungus only induces one SWEET transporter, , while represses most of the others (25). StSWEET7a was also induced during root colonization by the hemi-biotrophic fungus f. sp. . StSWEET7a which belongs to the clade II of SWEET transporters localized to the plasma membrane and transports glucose, fructose and mannose. Overexpression of in potato roots increased the strength of this sink as evidenced by an increase in the expression of the cell wall-bound invertase. Concomitantly, plants expressing were faster colonized by and by f. sp. . The increase in sink strength induced by ectopic expression of in roots could be abolished by shoot excision which reverted also the increased colonization levels by the symbiotic fungus. Altogether, these results suggest that AM fungi and spp. might induce to increase the sink strength and thus this gene might represent a common susceptibility target for root colonizing fungi.
丝状真菌在根部的定殖通过增强库强来改变植物体内的糖分分配。结果,糖转运蛋白发生转录重编程。在此,我们在马铃薯SWEET糖转运蛋白的特性及其对共生真菌和致病真菌定殖的响应调控方面取得了进一步进展。我们之前表明,丛枝菌根真菌在根部的定殖会诱导35个马铃薯SWEET基因发生主要的转录重编程,其中12个基因被诱导,10个基因被抑制。相比之下,我们在此表明,在早期定殖阶段,坏死营养型真菌仅诱导一个SWEET转运蛋白,同时抑制其他大多数(25个)。在根部被半活体营养型真菌f. sp.定殖期间,StSWEET7a也被诱导。属于SWEET转运蛋白进化枝II的StSWEET7a定位于质膜,转运葡萄糖、果糖和甘露糖。在马铃薯根中过表达会增强该库的强度,细胞壁结合型转化酶表达的增加证明了这一点。与此同时,过表达的植株被和f. sp.更快地定殖。通过切除地上部分可以消除根中异位表达诱导的库强增加,这也使共生真菌的定殖水平恢复到增加之前。总之,这些结果表明,丛枝菌根真菌和 spp.可能诱导来增加库强,因此该基因可能是根部定殖真菌的一个共同的易感性靶点。