1. An excreted small molecule promotes C. elegans reproductive development and aging.
- Author
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Ludewig AH, Artyukhin AB, Aprison EZ, Rodrigues PR, Pulido DC, Burkhardt RN, Panda O, Zhang YK, Gudibanda P, Ruvinsky I, and Schroeder FC
- Subjects
- Animals, Caenorhabditis elegans Proteins metabolism, Gene Expression Regulation, Developmental physiology, Hermaphroditic Organisms physiology, Male, Mutation, Signal Transduction, Aging physiology, Caenorhabditis elegans metabolism, Oviposition physiology
- Abstract
Excreted small-molecule signals can bias developmental trajectories and physiology in diverse animal species. However, the chemical identity of these signals remains largely obscure. Here we report identification of an unusual N-acylated glutamine derivative, nacq#1, that accelerates reproductive development and shortens lifespan in Caenorhabditis elegans. Produced predominantly by C. elegans males, nacq#1 hastens onset of sexual maturity in hermaphrodites by promoting exit from the larval dauer diapause and by accelerating late larval development. Even at picomolar concentrations, nacq#1 shortens hermaphrodite lifespan, suggesting a trade-off between reproductive investment and longevity. Acceleration of development by nacq#1 requires chemosensation and is dependent on three homologs of vertebrate steroid hormone receptors. Unlike ascaroside pheromones, which are restricted to nematodes, fatty acylated amino acid derivatives similar to nacq#1 have been reported from humans and invertebrates, suggesting that related compounds may serve signaling functions throughout metazoa.
- Published
- 2019
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