Blastomeres in C. elegans embryos execute lineage programs wherein the
fate of a cell is correlated reproducibly with the division sequence
by which that cell is born. We provide evidence that the pop-1 gene fu
nctions to link anterior-posterior cell divisions with cell fate decis
ions. Each anterior cell resulting from an anterior-posterior division
appears to have a higher level of nuclear POP-1 protein than does its
posterior sister. Genes in the C. elegans Wnt pathway are required fo
r this inequality in POP-1 levels. We show that loss of pop-1(+) activ
ity leads to several types of anterior cells adopting the fates of the
ir posterior sisters. These results suggest a mechanism for the invari
ance of blastomere lineages.