
Inducible depletion of PI(4,5)P2 by the synthetic iDePP system in Arabidopsis
Author(s) -
Mehdi Doumane,
Alexis Lebecq,
Léia Colin,
Aurélie Fangain,
Floris D Stevens,
Joseph Bareille,
Olivier Hamant,
Youssef Belkhadir,
Teun Munnik,
Yvon Jaillais,
MarieCécile Caillaud
Publication year - 2021
Publication title -
nature plants
Language(s) - English
Resource type - Journals
ISSN - 2055-0278
DOI - 10.1038/s41477-021-00907-z
Subject(s) - pi , arabidopsis , microbiology and biotechnology , phosphatidylinositol , biology , cytoskeleton , endocytic cycle , endocytosis , biochemistry , signal transduction , receptor , cell , gene , mutant
Phosphatidylinositol 4,5-bisphosphate (PI(4,5)P 2 ) is a low-abundance membrane lipid essential for plasma membrane function 1,2 . In plants, mutations in phosphatidylinositol 4-phosphate (PI4P) 5-kinases (PIP5K) suggest that PI(4,5)P 2 production is involved in development, immunity and reproduction 3-5 . However, phospholipid synthesis is highly intricate 6 . It is thus likely that steady-state depletion of PI(4,5)P 2 triggers confounding indirect effects. Furthermore, inducible tools available in plants allow PI(4,5)P 2 to increase 7-9 but not decrease, and no PIP5K inhibitors are available. Here, we introduce iDePP (inducible depletion of PI(4,5)P 2 in plants), a system for the inducible and tunable depletion of PI(4,5)P 2 in plants in less than three hours. Using this strategy, we confirm that PI(4,5)P 2 is critical for various aspects of plant development, including root growth, root-hair elongation and organ initiation. We show that PI(4,5)P 2 is required to recruit various endocytic proteins, including AP2-µ, to the plasma membrane, and thus to regulate clathrin-mediated endocytosis. Finally, we find that inducible PI(4,5)P 2 perturbation impacts the dynamics of the actin cytoskeleton as well as microtubule anisotropy. Together, we propose that iDePP is a simple and efficient genetic tool to test the importance of PI(4,5)P 2 in given cellular or developmental responses, and also to evaluate the importance of this lipid in protein localization.