In Caenorhabditis elegans, the early embryo contains five somatic foun
der cells (known as AB, MS, E, C and D) which give rise to very differ
ent lineages, Two simply produce twenty intestinal (E) or muscle (D) c
ells each, whereas the remainder produce a total of 518 cells which co
llectively contribute in a complex pattern to a variety of tissues(1).
A central problem in embryonic development is to understand how the d
evelopmental potential of blastomeres is restricted to permit the term
inal expression of such complex differentiation patterns, Here we iden
tify a gene, lit-1, that appears to play a central role in controlling
the asymmetry of cell division during embryogenesis in C. elegans. Mu
tants in lit-1 suggest that its product controls up to six consecutive
binary snitches which cause one of the two equivalent cells produced
at each cleavage to assume a posterior fate. Most blastomere identitie
s in C, elegans may therefore stem from a process of stepwise binary d
iversification.