Activin exhibits a potent mesoderm inducing activity towards the ectod
ermal tissue (animal cap) of Xenopus laevis blastulae. Thus in order t
o investigate the role of activin in morphogenesis of early Xenopus em
bryos, activation of genes for activin beta A and beta B was examined
by the reverse transcription polymerase chain reaction. In vivo, activ
in beta B mRNA appears to be present in embryonic stage 1 whereas beta
A mRNA is undetectable prior to gastrulation. beta B and beta A mRNAs
were noted to accumulate after stages 9 and 15 respectively. Activin
gene expression in Xenopus animal caps was examined after treatment wi
th various concentrations of activin A. Under these treatment conditio
ns, both activin beta A and beta B mRNAs accumulated in a dose-depende
nt fashion after 24 h. The same effect was noted for treatment with si
milar concentrations of activin B. Accumulation of mRNAs was inhibited
by the addition of cycloheximide to the culture medium, consistent wi
th the proposition that activin gene expression requires certain prote
in factors. In total, therefore, these data suggest that an autoinduct
ion mechanism is involved in the regulation of activin mRNA levels in
normal Xenapus embryos and that this mechanism may play a pivotal role
during early embryonic development.