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A Combinatorial Lipid Code Shapes the Electrostatic Landscape of Plant Endomembranes
MP. Platre, LC. Noack, M. Doumane, V. Bayle, MLA. Simon, L. Maneta-Peyret, L. Fouillen, T. Stanislas, L. Armengot, P. Pejchar, MC. Caillaud, M. Potocký, A. Čopič, P. Moreau, Y. Jaillais,
Language English Country United States
Document type Journal Article, Research Support, Non-U.S. Gov't
NLK
Cell Press Free Archives
from 2001-07-01 to 1 year ago
Free Medical Journals
from 2001 to 1 year ago
- MeSH
- Arabidopsis growth & development metabolism MeSH
- Cell Membrane metabolism MeSH
- Phosphatidylinositol Phosphates metabolism MeSH
- Phosphatidylserines metabolism MeSH
- Plant Roots growth & development metabolism MeSH
- Phosphatidic Acids metabolism MeSH
- Organelles MeSH
- Arabidopsis Proteins metabolism MeSH
- Signal Transduction MeSH
- Static Electricity * MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Membrane surface charge is critical for the transient, yet specific recruitment of proteins with polybasic regions to certain organelles. In eukaryotes, the plasma membrane (PM) is the most electronegative compartment of the cell, which specifies its identity. As such, membrane electrostatics is a central parameter in signaling, intracellular trafficking, and polarity. Here, we explore which are the lipids that control membrane electrostatics using plants as a model. We show that phosphatidylinositol-4-phosphate (PI4P), phosphatidic acidic (PA), and phosphatidylserine (PS) are separately required to generate the electrostatic signature of the plant PM. In addition, we reveal the existence of an electrostatic territory that is organized as a gradient along the endocytic pathway and is controlled by PS/PI4P combination. Altogether, we propose that combinatorial lipid composition of the cytosolic leaflet of organelles not only defines the electrostatic territory but also distinguishes different functional compartments within this territory by specifying their varying surface charges.
Bordeaux Imaging Center UMS 3420 CNRS US4 INSERM University of Bordeaux Bordeaux 33000 France
Institut Jacques Monod CNRS UMR 7592 Université Paris Diderot Sorbonne Paris Cité Paris 75013 France
Institute of Experimental Botany Czech Academy of Sciences 16502 Prague 6 Lysolaje Czech Republic
Metabolome Lipidome Facility of Bordeaux Functional Genomics Center Villenave d'Ornon France
References provided by Crossref.org
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