Published August 12, 2025 | Version Submitted v1
Discussion Paper Open

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

  • 1. ROR icon California Institute of Technology
  • 2. ROR icon Cornell University
  • 3. ROR icon Mount Holyoke College
  • 4. ROR icon SUNY Fredonia
  • 5. ROR icon Meiji University

Abstract

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.

Acknowledgement (English)

We acknowledge Nathan F. Dalleska and the Caltech Resnick Water and Environment Lab for the GC-MS analysis, and King L. Chow and the HKUST Environmental Central Facility for the initial GC-MS study. We thanks Jessica J. Sun for the initial phylogenetic tree analysis. We thank Joshua N. Muller for assisting with the imaging process. We also thank Erich Schwarz and Jae Cho for their assistance with WormBase data mining.

Contributions (English)

X.W. conceptualized and performed investigation (sample extraction, behavioral assays, GC-MS experiments); S.M.C. and H.P. designed and generated oac mutant strains with help from M.T.; Y.Y. and S. M. C. conducted metabolism experiments and analysis; A. G. designed and generated the oac reporter strains and R.M. performed the imaging. J. L and X. W. performed phylogenetic and sequence analysis. G.R.M., S.R. and X. W. performed the initial pheromone GC-MS study. X.W. and P.W.S. wrote the original draft; All authors reviewed and edited the manuscript; F.C.S. and P.W.S. supervised the project.

Copyright and License

The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission.

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Additional details

Funding

National Science Foundation
DGE-1745301
California Institute of Technology
Caltech Summer Undergraduate Research Fellowship -
National Institutes of Health
R24OD023041
National Institutes of Health
R24OD023041

Caltech Custom Metadata

Caltech groups
Division of Biology and Biological Engineering (BBE), Tianqiao and Chrissy Chen Institute for Neuroscience
Publication Status
Submitted