The endoderm of higher organisms is extensively patterned along the anterio
r/posterior axis. Although the endoderm (gut or E lineage) of the nematode
Caenorhabditis elegans appears to be a simple uniform tube, cells in the an
terior gut show several molecular and anatomical differences from cells in
the posterior gut. In particular, the gut esterase ges-l gene, which is nor
mally expressed in all cells of the endoderm, is expressed only in the ante
rior-most gut cells when certain sequences in the ges-1 promoter are delete
d. Using such a deleted ges-1 transgene as a biochemical marker of differen
tiation, we have investigated the basis of anterior-posterior gut patternin
g in C. elegans, Although homeotic genes are involved in endoderm patternin
g in other organisms, we show that anterior gut markers are expressed norma
lly in C. elegans embryos lacking genes of the homeotic cluster. Although s
ignalling from the mesoderm is involved in endoderm patterning in other org
anisms, we show that ablation of all non-gut blastomeres from the C. elegan
s embryo does not affect anterior gut marker expression; furthermore, ectop
ic guts produced by genetic transformation express anterior gut markers gen
erally in the expected location and in the expected number of cells. We con
clude that anterior gut fate requires no specific cell-cell contact but rat
her is produced autonomously within the E lineage. Cytochalasin D blocking
experiments fully support this conclusion. Finally, the HMG protein POP-1,
a downstream component of the Wnt signalling pathway, has recently been sho
wn to be important in many anterior/posterior fate decisions during C. eleg
ans embryogenesis (Lin, R,, Hill, R, J, and Priess, J, R, (1998) Cell 92, 2
29-239), When RNA-mediated interference is used to eliminate pop-1 function
from the embryo, gut is still produced but anterior gut marker expression
is abolished. We suggest that the C. elegans endoderm is patterned by eleme
nts of the Wnt/pop-1 signalling pathway acting autonomously within the E li
neage.