GeSUT4 mediates sucrose import at the symbiotic interface for carbon allocation of heterotrophic Gastrodia elata (Orchidaceae)

• Published in: Plant, cell and environment cell and environment, 2021-01, Vol.44 (1), p.20-33
• Main Authors: Ho, Li‐Hsuan, Lee, Yung‐I, Hsieh, Shu‐Ying, Lin, I‐Shiuan, Wu, Yun‐Chien, Ko, Han‐Yu, Klemens, Patrick A., Neuhaus, H. Ekkehard, Chen, Yi‐Min, Huang, Tzu‐Pi, Yeh, Chih‐Hsin, Guo, Woei‐Jiun
• Format: Article
• Language: English
• Subjects: Bacillus subtilis; Carbon; Complementation; Fungi; Gene expression; Homeostasis; Imports; Interfaces; Localization; mycoheterotrophy; Photosynthesis; Ribonucleic acid; RNA; Sucrose; Sucrose transporter; Sugar; SUT; symbiosis; transporter; Tubers; Yeasts
• ISSN: 0140-7791; 1365-3040
• DOI: 10.1111/pce.13833

Gastrodia elata, a fully mycoheterotrophic orchid without photosynthetic ability, only grows symbiotically with the fungus Armillaria. The mechanism of carbon distribution in this mycoheterotrophy is unknown. We detected high sucrose concentrations in all stages of Gastrodia tubers, suggesting sucrose may be the major sugar transported between fungus and orchid. Thick symplasm‐isolated wall interfaces in colonized and adjacent large cells implied involvement of sucrose importers. Two sucrose transporter (SUT)‐like genes, GeSUT4 and GeSUT3, were identified that were highly expressed in young Armillaria‐colonized tubers. Yeast complementation and isotope tracer experiments confirmed that GeSUT4 functioned as a high‐affinity sucrose‐specific proton‐dependent importer. Plasma‐membrane/tonoplast localization of GeSUT4‐GFP fusions and high RNA expression of GeSUT4 in symbiotic and large cells indicated that GeSUT4 likely functions in active sucrose transport for intercellular allocation and intracellular homeostasis. Transgenic Arabidopsis overexpressing GeSUT4 had larger leaves but were sensitive to excess sucrose and roots were colonized with fewer mutualistic Bacillus, supporting the role of GeSUT4 in regulating sugar allocation. This is not only the first documented carbon import system in a mycoheterotrophic interaction but also highlights the evolutionary importance of sucrose transporters for regulation of carbon flow in all types of plant‐microbe interactions. The fungus‐to‐plant carbon allocation in mycoheterotrophs represents an unique nutrient strategy. Characterizations of a plasma membrane/tonoplast‐localized Gastrodia GeSUT4 sucrose importer revealed sucrose allocation system during the mycoheterotrophic symbiosis, highlighting the importance of sucrose transporters for carbon allocation in plant–microbe interactions.