Sec1/Munc18 (SM) proteins are important regulators of SNARE complex assembly during exocytosis throughout all major animal tissue types. However, expression of a founding member of the SM family, UNC-18, is mostly restricted to the nervous system of the nematode C. elegans, where it is important for synaptic transmission. Moreover,
unc-18 null mutants do not display the lethality phenotype associated with (a) loss of all Drosophila and mouse orthologues of
unc-18 and (b) with elimination of synaptic transmission in C. elegans. We investigated whether a previously uncharacterized
unc-18 paralogue, which we named
uncp-18, may be able to explain the restricted expression and limited phenotypes of
unc-18 null mutants. A reporter allele shows ubiquitous expression of
uncp-18. Analysis of
uncp-18 null mutants,
unc-18 and
uncp-18 double null mutants, as well as overexpression of
uncp-18 in an
unc-18 null mutant background, shows that these two genes can functionally compensate for one another and are redundantly required for embryonic viability. Our results indicate that the synaptic transmission defects of
unc-18 null mutants cannot necessarily be interpreted as constituting a null phenotype for SM protein function at the synapse.