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Published March 26, 2023 | Submitted
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PEZO-1 and TRP-4 mechanosensors are involved in mating behavior in Caenorhabditis elegans

Abstract

Male mating in Caenorhabditis elegans is a complex behavior with a strong mechanosensory component. C. elegans has several characterized mechanotransducer proteins, but few have been shown to contribute to mating. Here, we investigated the roles of PEZO-1, a piezo channel, and TRP-4, a mechanotransducing TRPN channel, in male mating behavior. We show that pezo-1 is expressed in several male-specific neurons with known roles in mating. We show that, among other neurons, trp-4 is expressed in the PCA sensory neuron, which monitors relative sliding between the male and the hermaphrodite and inhibits neurons involved in vulva detection. Mutations in both genes compromise many steps of mating, including initial response to the hermaphrodite, scanning, turning, and vulva detection. We performed pan-neuronal imaging during mating between freely-moving mutant males and hermaphrodites. Both pezo-1 and trp-4 mutants showed spurious activation of the sensory neurons involved in vulva detection. In trp-4 mutants, this spurious activation might be caused by PCA failure to inhibit vulva-detecting neurons during scanning. Indeed, we show that without functional TRP-4, PCA fails to detect the relative sliding between the male and hermaphrodite. Cell-specific TRP-4 expression restores PCA's mechanosensory function. Our results demonstrate new roles for both PEZO-1 and TRP-4 mechanotransducers in C. elegans mating behavior.

Additional Information

The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY-ND 4.0 International license. We thank WormBase for genome information, CGC for providing strains, Ian Kimbell for help with data collecting, Xiaofei Bai for providing AG570 pezo-1(av240), Shawn Xu for sharing a plasmid containing trp-4, and Tsui-Fen Chou for providing Cas9 protein. This work was supported by NIH R01-NS113119 (PWS and ADTS). KB was supported by NIH-Training Grant T32GM007616. The authors have declared no competing interest.

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Additional details

Created:
August 20, 2023
Modified:
December 13, 2023