Biology subjects

Largeau, C.

Publications and source records attributed to Largeau, C..

4 recordsLinked to original sources

bioRxiv2026

PDZD-8 interacts with LGG-2/LC3 to promote autolysosome formation

LGG-2/LC3 and LGG-1/GABARAP are members of the Atg8 ubiquitin-like protein family, playing central roles in autophagy. Through a yeast two-hybrid screen, we identified the endoplasmic reticulum protein PDZD-8 as a novel interactor of the C. elegans autophagy protein LGG-2/LC3. We demonstrate that PDZD-8 binds specifically to LGG-2 and not LGG-1 via a canonical LC3-interacting region (LIR) and colocalizes with LGG-2-positive autophagosomes in vivo. Loss of PDZD-8 leads to a transient accumulation of enlarged LGG-2-positive autophagosomes that remain closely associated with lysosomes. Genetic disruption of core autophagy genes suppresses the pdzd-8 mutant phenotype, indicating that this phenotype is dependent on autophagy. Moreover, loss of rab-7, which blocks autophagosome-lysosome fusion, also suppresses the pdzd-8 phenotype, suggesting that the RAB-7-dependent fusion step is epistatic to PDZD-8 and that PDZD-8 acts downstream of autophagosome-lysosome maturation. Microscopy approaches (TEM, CLEM, and FIB-SEM) reveal an accumulation of fused autophagosome-lysosome structures, pointing to a transient block in autophagic flux in pdzd-8 mutants. Furthermore, PDZD-8 lacking either the SMP lipid-transfer domain or the LIR motif phenocopies the pdzd-8 null mutant, underscoring the importance of both domains. Our findings support a model in which PDZD-8, in conjunction with LGG-2/LC3, mediates ER-autophagosome/autolysosome contacts that are critical for subsequent autolysosome completion. Significance StatementAutophagy is a conserved cellular degradation pathway essential for maintaining homeostasis and responding to stress. Although the molecular machinery driving autophagosome formation and fusion with lysosomes is relatively well-characterized, the contribution of membrane contact sites to autophagic flux remains poorly understood. Here, we identify PDZD-8, an endoplasmic reticulum (ER) protein, as a novel interactor of the Caenorhabditis elegans LC3/Atg8 homolog LGG-2. We show that PDZD-8 regulates the completion of autolysosome maturation by bridging ER-autophagosome/autolysosome contacts. Loss of PDZD-8 results in the accumulation of enlarged autophagosomes adjacent to lysosomes and a transient block in autophagic flux, a phenotype that depends on the RAB-7-mediated tethering step. These findings reveal a previously unrecognized role for PDZD-8 in coordinating ER-autophagosome/autolysosome dynamics during autophagy.

cell biology↗

bioRxiv2024

Reticulon dependent ER-phagy mediates adaptation to heat stress in Caenorhabditis elegans

The selective degradation of ER by autophagy, named ER-phagy, promotes the recovery of ER homeostasis after a stress. Depending on the ER stress, different types of ER-phagy involve various selective autophagy receptors. In this study, we report a macroER-phagy induced by the fragmentation of tubular ER in response to acute heat stress. We identified a novel ER-phagy receptor encoded by the reticulon long isoform RET-1d. RET-1d is mainly expressed in the nervous system and the epidermis and colocalize with the ubiquitin-like autophagy protein LGG-1/GABARAP during heat stress induced autophagy. Two LIR motifs in the long intrinsically disordered region of RET-1d mediate its interaction with LGG-1 protein. The specific depletion of RET-1d isoform resulted in a delay in autophagosome biogenesis and a decrease in the capacity of animals to adapt to heat stress. Our data revealed a RET-1d dependent ER-phagy mechanism that takes place in neurons and epidermis and participates to the adaptation of C. elegans to heat stress.

cell biology↗

bioRxiv2022

Molecular determinants of inhibition of UCP1-mediated respiratory uncoupling

Brown adipose tissue expresses uncoupling protein 1 (UCP1), a mitochondrial transporter that uncouples respiration from ATP synthesis and dissipates energy as heat, making it a target for treating obesity and related metabolic disorders. Here, we combine molecular dynamics simulations with mitochondrial respiration assays to investigate how purine nucleotides inhibit respiration uncoupling by UCP1. Simulations predict that GDP binds UCP1 in the common substrate binding site in an upright orientation, where the base moiety interacts with a pair of charged residues (R92/E191) that are specifically conserved in the subfamily of UCPs. E191, among others, interacts with purine but not pyrimidine bases, suggesting a rationale for nucleotide specificity in UCP1 inhibition. We also identify a triplet of uncharged residues involved in hydrophobic contacts with GDP. Site-directed mutagenesis of either I187 or W281 to alanine increases lauric acid-induced uncoupling activity of UCP1 and partially suppresses inhibition of UCP1 activity by GDP in yeast spheroplasts. The triple mutant (F88, I187, W281) to alanine is overactivated by lauric acid even in a high concentration of purine nucleotides. Variants at these positions may help increase energy expenditure in a cellular and therapeutic context.

biophysics↗

bioRxiv2021

LGG-1/GABARAP lipidation is dispensable for autophagy and development in C .elegans

The ubiquitin-like proteins Atg8/LC3/GABARAP are required for multiple steps of autophagy such as initiation, cargo recognition and engulfment, vesicle closure and degradation. Most of LC3/GABARAP functions are considered dependent on their post-translational modifications and addressing to membranes through a conjugation to a lipid, the phosphatidylethanolamine. Contrarily to mammals, C. elegans possesses single homologs of LC3 and GABARAP families, named LGG-2 and LGG-1. Using site directed mutagenesis, we inhibited the conjugation of LGG-1 to the autophagosomal membrane and generated mutants that express only cytosolic forms, either the precursor or the cleaved protein. LGG-1 is an essential gene for autophagy and development in C. elegans, but we discovered that its functions could be fully achieved independently of its localization to the membrane. This study reveals an essential role for the cleaved form of LGG-1 in autophagy but also in an autophagy independent embryonic function. Our data question the use of the lipidated GABARAP/LC3 as the main marker of autophagic flux and highlight the high plasticity of autophagy.

cell biology↗