Tenascin is believed to be an important extracellular matrix protein i
nvolved in regulating numerous developmental processes, such as morpho
genetic cell migration and organogenesis. This function was implied by
its tissue distribution and regulated expression during embryogenesis
. However, such an important function was questioned recently, since m
ice lacking a functional tenascin gene apparently developed normally.
To us, this is not conclusive evidence that tenascin has no function,
for we believe that the loss of tenascin could be compensated for. Sin
ce in several other cases compensation occurs by other members of a ge
ne family, we started to investigate the family of tenascin-like genes
and we review in this article the structures of the original tenascin
/cytotactin (tenascin-C), restrictin/J-160/180 (tenascin-R), and the t
enascin-like gene present in the major histocompatibility complex clas
s III locus (tenascin-X). Furthermore, we present evidence for the lik
ely existence of even more members of this tenascin family.