Cellular communication in the developing embryo is mediated by recepto
r-ligand interactions at the cell surface. Receptor protein tyrosine k
inases (RTKs) have been shown to play a critical role in the developme
nt of the vertebrate embryo. The eph receptors are a large subclass of
RTKs for which a corresponding ligand family has only recently been d
escribed. The restricted expression patterns of several eph receptors
imply roles for these molecules in early vertebrate development. We ha
ve isolated both a ligand of the eph ligand family (ELF), that we have
named XELF-a, and an eph-related receptor, XE10, the likely homolog o
f the murine eck/Sek-2 receptor. At least two forms of the XELF-a tran
script are present in the developing embryo. A truncated form of the X
ELF-a ligand, XELF-a', is the first ELF ligand isolated that lacks bot
h the membrane-spanning and membrane-anchoring motifs conserved among
this family, suggesting that ELF ligands can function as fully soluble
molecules in vivo. XELF-a and XE10 are expressed maternally and throu
ghout early embryogenesis, while XELF-a' is only expressed zygotically
. The dynamic expression patterns of these signalling molecules, in bo
th mesoderm and neurectoderm, suggest that they may play a role in the
patterning of the early vertebrate embryo.