From egg through adult, C. elegans has six life stages including an op
tion for dauer formation and diapause at larval stage L3 in adverse en
vironments. Somatic cells throughout the organism make consistent choi
ces and advance in unison, suggesting a mechanism of coordinate regula
tion at these stage transitions. Earlier studies showed that daf-12, w
hich encodes a nuclear receptor (W. Yeh, 1991, Doctoral Thesis. Univer
sity of Missouri-Columbia), regulates dauer formation; epistasis exper
iments placed daf-12 near the end of the dauer signaling pathway. Here
we describe novel daf-12 alleles that reveal a general role in advanc
ing L3 stage programs. In these mutants, somatic cells repeat L2-speci
fic cellular programs of division and migration at the L3 stage; epist
asis experiments place daf-12 between lin-14 and lin-28 Within the het
erochronic pathway. We propose daf-12 and other heterochronic genes pr
ovide cellular memories of chronological stage for selecting stage-app
ropriate developmental programs. Endocrine factors could coordinate th
ese stage transitions and specify developmental alternatives.