We have used in vitro cultures initiated from immature zygotic embryos
of the monocot Triticum aestivum, variety Chinese Spring, to investig
ate some features of the transcriptional regulation of the Em gene. A
210-bp cDNA fragment internal to the coding region of the Em gene was
amplified by PCR, cloned and used as a probe in northern analyses. Em
gene expression was found to be associated with cultures displaying an
embryogenic potential and, more precisely, with the presence of somat
ic embryos. The time-course of Em gene expression was thereafter monit
ored, by PCR and northern analysis, from the initiation of cultures un
til the appearance of embryogenic structures and was shown to be tempo
rally regulated during the somatic embryogenesis process. Finally, the
Fm protein was observed in both somatic embryos and embryogenic cultu
res whereas it was not detected in non-embryogenic cultures. Our resul
ts, obtained from a monocot, ask the question of whether Em gene expre
ssion could be used as a universal late marker of somatic embryogenesi
s.