We have identified a homolog of the mammalian p53 tumor suppressor protein
in the nematode Caenorhabditis elegans that is expressed ubiquitously in em
bryos. The gene encoding this protein, cep-1, promotes DNA damage-induced a
poptosis and is required for normal meiotic chromosome segregation in the g
erm line. Moreover, although somatic apoptosis is unaffected, cep-1 mutants
show hypersensitivity to hypoxia-induced lethality and decreased longevity
in response to starvation-induced stress. Overexpression of cep-1 promotes
widespread caspase-independent cell death, demonstrating the critical impo
rtance of regulating p53 function at appropriate levels. These findings sho
w that C. elegans p53 mediates multiple stress responses in the soma, and m
ediates apoptosis and meiotic chromosome segregation in the germ line.