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TPS Proteins coordinate plant growth with sugar availability via the SnRK1 Kinase

Reis-Barata, D.; Confraria, A.; Margalha, L.; Peixoto, B.; Lopes, F. L.; Belda-Palazon, B.; Jurke, B.; Arrivault, S.; Shukla, V.; Feil, R.; Licausi, F.; Kaschani, F.; Kaiser, M.; Caldana, C.; Stitt, M.; Lunn, J. E.; Baena-Gonzalez, E.

2025-08-20 plant biology
10.1101/2025.08.17.670254 bioRxiv
Show abstract

The ability to sense and respond to nutrients determines adaptation and survival in all organisms. In plants, sucrose stimulates growth and developmental progression via the signalling sugar trehalose 6-phosphate (T6P) which reflects sucrose availability. T6P acts, at least partly, by inhibiting the protein kinase SUCROSE NON-FERMENTING 1 (SNF1)-RELATED KINASE 1 (SnRK1) but the underlying mechanisms are poorly understood. Here, we identify a group of catalytically inactive T6P synthase (TPS) proteins, TPS5/6/7, as important factors for coupling the T6P signal to SnRK1 activity. In Arabidopsis thaliana, lack of TPS5/6/7 causes severe growth defects, particularly in roots. This is accompanied by a metabolic signature that is suggestive of T6P insensitivity and impaired sucrose utilization. Using a combination of genetics, SnRK1 activity assays, and imaging, we demonstrate that the growth defects of the tps5/6/7 mutant are due to SnRK1 misregulation and are reverted by knocking-down SnRK1 in this background. Co-immunoprecipitation assays further show that T6P promotes the interaction of TPS proteins with SnRK1 in a highly specific and dose-dependent manner. Our results support a model where TPS proteins act as T6P sensors, inhibiting non-nuclear SnRK1 activity when sucrose is abundant to promote biosynthetic processes and growth.

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