Novel intracellular trafficking pathway discovered in plant cells

Sadie Harley
scientific editor

Robert Egan
associate editor

Just like in yeast and animal cells, vacuoles in plants are responsible for breaking down unwanted cellular components. At the same time, vacuoles in seeds also serve the opposite role—storing large amounts of proteins that provide energy during germination.
These storage proteins, accumulated in the vacuoles of seeds such as beans and wheat, are not only vital for plant growth but also represent an important agricultural resource closely tied to our daily diet.
Until now, it was entirely unknown whether proteins could be transported from the vacuole to other organelles.
In a study in Nature Plants, Dr. Yihong Feng (Specially Appointed Assistant Professor) and Professor Takashi Ueda at the National Institute for Basic Biology in Japan, together with their collaborators, demonstrate in the model plant Arabidopsis thaliana the existence of a retrograde trafficking pathway that retrieves the membrane protein VAMP727 from the vacuolar membrane back to endosomes. The team further identifies the molecular machinery responsible for this pathway.
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Top panels: Root epidermal cells expressing Venus-VAMP727 and mRFP-VAMP721 in wild type (left) and the snx1 mutant (right). The punctate localization pattern of VAMP721, which functions in the secretory pathway, remained unchanged in the snx1 mutant. In contrast, VAMP727 accumulated at the vacuolar membrane in the snx1 background. Scale bar = 10 µm. Bottom panels: Images acquired using the super-resolution confocal live imaging microscope (SCLIM) of mGFP-VAMP727 (yellow), SNX1-mRFP (magenta), and the vacuolar membrane marker miRFP-SYP22 (cyan). These images capture the budding of VAMP727 together with SNX1 from the vacuolar membrane. Grid size = 0.942 µm. Credit: Ueda Lab, NIBB -
Images acquired using the SCLIM of VPS35b-iRFP (core retromer, cyan), SNX1-mRFP (magenta), and the endosomal marker GFP-ARA7 (yellow). Time-lapse observations revealed budding of VPS35b from the endosomal membrane, which did not include SNX1. Grid size = 0.426 µm. Credit: Ueda Lab, NIBB
Dr. Feng commented, "The sorting nexin proteins that function in this newly discovered pathway have independently diversified in plants compared to animals and yeast. Our findings indicate that this trafficking route is a plant-specific innovation."
Professor Ueda added, "We were able to show that the plant-unique membrane fusion protein VAMP727 co-evolved with a recycling mechanism from the vacuole. This suggests that the evolution of vacuolar protein transport in seed plants, which is essential for massive storage protein accumulation, was closely tied to the emergence of this retrograde pathway."
This study reveals part of the unique membrane trafficking network that plants have evolved during their history, providing new insights into both cell biology and plant science.
More information: Yihong Feng et al, Retrieval from vacuolar and endosomal compartments underpinning the neofunctionalization of SNARE in plants, Nature Plants (2025).
Journal information: Nature Plants
Provided by National Institutes of Natural Sciences