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Groaz, A.

Publications and source records attributed to Groaz, A..

4 recordsLinked to original sources

Identification of srh-30 as a 2-nonanone receptor in C. elegans

C. elegans detects food, mates, and danger through a large repertoire of chemosensory receptors. The volatile odorant 2-nonanone is a well-established aversive stimulus that reliably elicits avoidance chemotaxis. However, the receptor(s) responsible for its detection have not been identified. Here, we leveraged CeNGEN single-cell expression profiles to identify candidate receptors required for sensing 2-nonanone. We narrowed the list of candidate chemoreceptor genes by selecting genes expressed in the aversive amphid neurons AWB and ASH while excluding genes expressed in other amphid sensory neurons. We tested available mutants from the C. elegans Genetics Center (CGC) and identified srh-30 as a candidate required for normal 2-nonanone avoidance. Two independent srh-30 null alleles generated using CRISPR-Cas9 confirmed that loss of srh-30 causes a partial defect in 2-nonanone sensing. srh-30 promoter-driven fluorescent reporter, mKate, localized to the distal tips of AWB sensory cilia, consistent with a direct sensory role. Finally, ectopic expression of srh-30 in the attractive AWA neuron shifted the behavioral response to 2-nonanone toward neutrality, supporting srh-30 as a sensory receptor. Together, these results identify srh-30 as a sensory receptor mediating 2-nonanone-evoked avoidance and demonstrate a transcriptome-guided strategy for mapping odor receptors.

neuroscience↗

O-Acyltransferase Genes Involved in the Production of Volatile Sex Pheromones in Caenorhabditis elegans

Gene family expansions are critical for functional diversification, yet paralog contributions to metabolic pathways are often unclear. In Caenorhabditis, the expanded O-acyltransferase (OAC) family--enzymes that transfer acyl groups to hydroxylated substrates--remains poorly characterized despite having been implicated in lipid metabolism. Using CRISPR-Cas9 mutagenesis, behavioral assays, gas chromatographic-mass spectral (GC-MS) analyses, and metabolomics, we systematically analyzed 59 OAC-family protein-coding genes to define their roles in regulating signaling molecules. We found that four adjacent paralogs (oac-13, oac-16, oac-25, and oac-28) on chromosome I are required for synthesizing volatile sex pheromones (VSPs)--airborne signals critical for male mate-searching. Specifically, oac-13 and oac-16 are necessary for producing both major pheromone components, while the identical tandem paralogs oac-25 and oac-28 regulate the production of the later-eluting component in gas chromatography. Disruption of these genes reduced production of key pheromone components and impaired male attraction. Metabolomics revealed that oac-16 and other OACs also modulate synthesis and secretion of non-volatile ascaroside pheromones, indicating dual roles in chemical signaling. This work uncovers functional specialization within an expanded gene family, illustrating how redundancy and divergence enable adaptive evolution of communication systems.

biochemistry↗

Efficient pheromone navigation via antagonistic detectors

Chemotaxis to a moving potential mate that emits a volatile sex pheromone poses a navigation challenge requiring rapid, precise responses to maximize reproductive success. Volatile chemicals form gradients that differ from soluble compounds, potentially making navigation based on comparisons between spatially separated sensors unreliable for small-bodied animals. Here we show that, rather than a simple spatial comparison, Caenorhabditis elegans males employ an antagonistic strategy, comparing inputs from sex-shared head (AWA) and male-specific tail (PHD) sensory neurons with distinct response properties. Despite sharing a receptor, SRD-1, these detectors play different roles: AWAs promote forward movement and acceleration, while PHDs induce reversals and deceleration. In rising pheromone gradients, AWA activity dominates; in falling gradients, AWA inactivates, allowing PHD to correct trajectories. AWAs are essential for mate-searching, while PHDs are crucial for complex tasks. A minimal computational model reproduces these behaviors and infers how head-tail signals are combined. Thus, a sexually dimorphic, antagonistic sensory system enables adaptive navigation in dynamic environments

neuroscience↗

Actin crosslinker competition and sorting drive emergent GUV size-dependent actin network architecture

How complex actin network architectures arise and coexist in membrane-enclosed cell environment remains unknown. By encapsulating actin and crosslinking proteins -actinin and fascin in giant unilamellar vesicles (GUVs), we show that physical confinement and its size can lead to formation of complex actin structures, including rings and asters at GUV peripheries and centers. Strikingly, we find that the materials properties of the aster structures depend on the ratio of the relative concentrations of -actinin and fascin, and we demonstrate that this results from -actinin and fascin sorting into separate domains in the structures. We complement our experiments with molecular simulations that capture the spontaneous formation of competing network architectures; these provide a microscopic view of the dynamics and delineate the molecular features that promote sorting. We propose that the observed boundary-imposed effect on protein sorting is a general mechanism for creating emergent structures in biopolymer networks with multiple crosslinkers.

biophysics↗