Functionally redundant genes present a puzzle as to their evolutionary preservation, and offer an interesting opportunity for molecular specialization. In Caenorhabditis elegans, either one of two presenilin genes (
sel-12 or
hop-1) facilitate Notch activation, providing the catalytic subunit for the gamma secretase proteolytic enzyme complex. For all known Notch signaling events,
sel-12 can mediate Notch activation, so the conservation of
hop-1 remains a mystery. Here, we uncover a novel "late-onset" germline Notch phenotype in which HOP-1-deficient worms fail to maintain proliferating germline stem cells during adulthood. Either SEL-12 or HOP-1 presenilin can impart sufficient Notch signaling for establishment and expansion of the germ line, but maintenance of an adult stem cell pool relies exclusively on HOP-1-mediated Notch signaling. We also show that HOP-1 is necessary for maximum fecundity and reproductive span. The low fecundity phenotype of
hop-1 mutants can be phenocopied by switching off
glp-1/Notch function during the last stage of larval development. We propose that at the end of larval development, dual presenilin usage switches exclusively to HOP-1, perhaps offering opportunities for differential regulation of the germ line during adulthood. Additional defects in oocyte size and production rate in
hop-1 and
glp-1 mutants indicate that the process of oogenesis is compromised when germline Notch signaling is switched off. We calculate that in wild-type adults, as much as 86% of cells derived from the stem cell pool function to support oogenesis. This work suggests that an important role for Notch signaling in the adult germ line is to furnish a large and continuous supply of nurse cells to support the efficiency of oogenesis.