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Lupette, J.

Publications and source records attributed to Lupette, J..

2 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↗