The C. elegans defecation cycle is characterized by the contraction of thre
e distinct sets of muscles every 50 s. Our data indicate that this cycle is
regulated by periodic calcium release mediated by the inositol trisphospha
te receptor (IP3 receptor). Mutations in the IF, receptor slow down or elim
inate the cycle, while overexpression speeds up the cycle. The IP3 receptor
controls these periodic muscle contractions nonautonomously from the intes
tine. In the intestinal cells, calcium levels oscillate with the same perio
d as the defecation cycle and peak calcium levels immediately precede the f
irst muscle contraction. Mutations in the IF, receptor slow or eliminate th
ese calcium oscillations. Thus, the IP3 receptor is an essential component
of the timekeeper for this cycle and represents a novel mechanism for the c
ontrol of behavioral rhythms.