In Arabidopsis thaliana (L.) Heynh, the mutation in ERECTA is known to
confer a compact inflorescence by a reduction in the lengths of inter
nodes and pedicels. We analyzed the expression pattern of this gene du
ring plant development. In site hybridization and histochemical analys
is using transgenic plants carrying chimeric gene fusions, with the ER
ECTA promoter fused to the P-glucuronidase (GUS) gene, showed that ERE
CTA was predominantly expressed in the shoot apical meristems and orga
n primordia. ERECTA expression in the shoot apical meristem was weak e
arly in plant development but increased with the transition from the v
egetative to the reproductive growth phase. ERECTA was also strongly e
xpressed in organ primordia and immature organs but weakly in mature o
rgans. Thus, ERECTA was expressed in a cell-specific and developmental
ly regulated manner. In order to identify the regulatory mechanism res
ponsible for the expression pattern of ERECTA, the cis-acting regions
in the ERECTA promoter were defined by study of the expression of the
chimeric genes that consist of the 5'- or internal deleted promoter an
d a GUS reporter gene in transgenic plants. The results showed that th
e essential cis-regulatory elements governing the spatially and tempor
ally specific expression of ERECTA are located between positions -462
and -228 bp and between positions -228 and -153 bp with respect to the
transcriptional initiation site.