Related Experiment Video
Updated: Jun 5, 2026

In Vivo Visualization of Calcium Transients during Fertilization and Early Development in C. elegans
Published on: July 12, 2024
Characterization of spe-40/Fam187 identifies a deeply conserved sperm protein at the C. elegans fertilization synapse
Jeyashree Nathan Elango1, Isaac H Shin1, Anushree Gurjar1
1Department of Biological Sciences, University of Delaware, Newark, DE 19716, USA.
Abstract:
Fertilization is the process in which two specialized cells, the sperm and egg, interact, adhere, and fuse their membranes. This occurs in all sexually reproducing organisms. Several transmembrane and secreted proteins have been shown to be required for fertilization. Genetic mutations can alter these proteins and disrupt fertilization, leading to reduced or no offspring. When fertilization-specific sperm proteins are mutated, sperm production, motility, and activation are unaffected, but the sperm lose the ability to successfully fertilize an egg. In this study, we report on the sperm-specific protein SPE-40/FAM187, which is a single-pass transmembrane protein with an immunoglobulin-like domain. When spe-40 is mutated in C. elegans the animals are severely sub-fertile due to a sperm-specific defect. All the characteristics of the sperm that we have evaluated in the mutant are normal, yet sperm lacking SPE-40 do not fertilize. SPE-40 has orthologs in other species, including humans. Thus, we have established a role for SPE-40/FAM187 in fertilization that suggests it represents a conserved component of the fertilization synapse.
Related Concept Videos
Fertilization
Meiosis I

