DAF-18/PTEN prevents oocyte wastage in spermless C. elegans hermaphrodites by blocking spermatheca neck dilation through RHO-1/RhoA disinhibition

Loss of the Phosphatase and TENsin homolog PTEN drives cancer in humans. In C. elegans hermaphrodites that lack sperm, the PTEN ortholog DAF-18 is required for oocyte quiescence and their proximal accumulation, along with the concomitant homeostatic downregulation of germline stem cell proliferation. As such, spermless daf-18(ø) mutants undergo full-scale oogenesis and ovulation in a futile manner, wasting all produced oocytes. When oocyte laying is prevented in these mutants, oocytes hyperaccumulate to form differentiated benign tumors. Here, we show that daf-18 expression in the spermatheca neck myoepithelium is sufficient to induce oocyte arrest and homeostatic downregulation of germline stem cell proliferation in spermless hermaphrodites, altogether prohibiting tumorigenesis. We demonstrate that DAF-18 promotes spermatheca neck contractility through limiting PIP ₃ levels and AKT activity, preventing the latter from inactivating RHO-1/RhoA by direct phosphorylation at a conserved site. Loss of PTEN may therefore promote benign tumorigenesis in humans through similar cell non-autonomous effects.