The paternal-effect embryonic-lethal gene, spe-11, is required for nor
mal development of early C. elegans embryos, Spe-11 embryos fail to co
mplete meiosis, form a weak eggshell, fail to orient properly the firs
t mitotic spindle, and fail to undergo cytokinesis, Here we report clo
ning and sequencing of the spe-11 gene, which encodes a novel protein.
As predicted by the paternal-effect mutant phenotype, the gene is exp
ressed during spermatogenesis but is not detectable in females undergo
ing oogenesis, and the protein is present in mature sperm. To investig
ate whether SPE-11's essential function is during spermatogenesis or w
hether sperm-delivered SPE-11 functions in the newly fertilized embryo
, we engineered animals to supply SPE-11 to the embryo through the ooc
yte rather than through the sperm, We found that maternal expression i
s sufficient for embryonic viability, This result demonstrates that SP
E-11 is not required during spermatogenesis, and suggests that SPE-11
is a sperm-supplied factor that participates directly in development o
f the early embryo, In contrast to the many known maternal factors req
uired for embryogenesis, SPE-11 is the first paternally contributed fa
ctor to be genetically identified and molecularly characterized.