bioRxiv Science⌕ Search

Biology subjects

Castets, J.

Publications and source records attributed to Castets, J..

3 recordsLinked to original sources

Unveiling the molecular identity of plant autophagic compartments: A proteo-lipidomic study in Arabidopsis thaliana

Autophagy is an intracellular degradation and recycling pathway essential for cell quality control and plant tolerance to stress. The formation and maturation of autophagosomes, the cargo-packing vesicles, rely on extensive membrane remodeling, yet little is known about the nature, dynamics and functions of lipids in these events. Here, we established a method combing cell fractionation and immuno-isolation in native conditions to purify autophagic membranes from Arabidopsis thaliana. By integrating proteomic and lipidomic analyses, we defined their molecular footprint which, coupled to colocalization analyses, revealed potent actors involved in lipid metabolism, membrane trafficking and membrane remodeling, supporting a close interplay between lipid homeostasis and autophagosome biology. Characterization of the phagophore lipid composition showed low sterol and sphingolipid content, a predominance of glycerophospholipids, including phosphoinositides, and a particular enrichment in phosphatidylcholine and phosphatidylglycerol. Comparisons with other plant endomembranes and autophagic compartments from other organisms revealed the singularity of this lipid signature and notably identified phosphatidylglycerol as a plant-specific component of autophagic membranes. Analyses of inducible phosphatidylglycerol-deficient plants showed defects in autophagy activity thereby supporting the functional relevance of the phagophore lipid composition, particularly that of phosphatidylglycerol homeostasis. Together, our findings place lipids as fundamental components of the autophagy molecular landscape and provide a framework to further investigate their contribution to autophagosome biology and functions in plant acclimation to environmental changes. Significance StatementAutophagy is catabolic pathway critical for eukaryotic life and essential for plant acclimation to stress. It hinges on the remarkable plasticity of a specialized membrane, the phagophore, to orchestrate and support intense membrane remodeling events towards the formation of the autophagic vesicle containing cargo. To resolve their elusive molecular bases, we need to integrate inputs from both components of biological membranes: proteins and lipids, yet information regarding lipids is still very limited. Here, we isolated plant phagophores, established their protein and lipid molecular footprint, revealed its singularity and showed its physiological and functional relevance for autophagy activity. Our work highlights lipids as key regulators of plant autophagy and opens new doors for investigating how membrane dynamics shape cellular stress responses.

plant biology↗

A dual component system instructs membrane hydrolysis during the final stages of plant autophagy

Autophagy is an intracellular catabolic process conserved across eukaryotes and critical for plant stress tolerance. Upon their delivery in the vacuole, how autophagic bodies containing cargo are hydrolyzed to warrant autophagy degradation remains poorly characterized. Here, we identify two Arabidopsis phospholipases as core components of the autophagy machinery. We find that LCAT3 and LCAT4 traffic to the vacuolar lumen and converge on autophagic bodies using differential pathways, placing them on the outer and inner side of the vesicle, respectively. Double knockouts lcat3,4 accumulate autophagic bodies and show reduced autophagy activity. In vivo reconstitution demonstrates that LCAT3 can hydrolyze the membrane of autophagic bodies, enabling the activity of LCAT4 to enhance this process. In sum, our work reveals that the concerted action of a multi-component system is required for the efficient and specific disruption of autophagic bodies as an obligatory step for the completion of the autophagy pathway.

plant biology↗

AtVPS13M1 is involved in lipid remodeling in low phosphate and is located at the mitochondria surface in plants

VPS13 are conserved lipid transporters with multiple subcellular localizations playing key roles in many fundamental cellular processes. While the localization and function of VPS13 have been extensively investigated in yeast and animals, little is known about their counterparts in plants, particularly regarding their role in stress response. In this study, we characterized AtVPS13M1, one of the four VPS13 paralogs of the flowering plant Arabidopsis thaliana. We show that AtVPS13M1 binds and transports glycerolipids with a low specificity in vitro. AtVPS13M1 interferes with phospholipids degradation in response to phosphate starvation, a nutrient stress that triggers a massive remodeling of membrane lipids. AtVPS13M1 is mainly expressed in young dividing and vascular tissues. Finally, we show that AtVPS13M1 is mainly located at the surface of mitochondria in leaves. Overall, our work highlights the conserved role in lipid transport of VPS13 in plants, reveals their importance in nutrient stress response and opens important perspectives for the understanding of lipid remodeling mechanisms and for the characterization of this protein family in plants.

cell biology↗