In Antirrhinum majus, one proposed role of the gene fimbriata (fim) is as a
mediator between the floral meristem identify gene floricaula (flo) and fl
oral organ identity genes such as deficiens (def) and plena (ple). The mech
anism of firn activity is probably unique as, while the other genes in the
hierarchy are thought to be transcription factors, firn is thought to targe
t proteins to a ubiquitin-mediated destruction pathway. Both flo and def ha
ve been shown to act non-cell autonomously. We tested the hypotheses that (
i) fim acts in a non-cell autonomous manner; and (ii) non-cell autonomy of
flo might be through activation and subsequent non-cell autonomous activity
of firn. Plants bearing an unstable fim allele were monitored for revertan
t shoots. Analysis of firn RNA expression in plants derived from revertant
shoots, and segregation of revertant phenotype in progeny from revertant pl
ants, indicated that all were periclinal chimeras with wild-type fim expres
sion only in subepidermal layers. Despite the absence of fim in the epiderm
al layer, expression of downstream genes was normal, suggesting non-cell au
tonomous activity of fim. Subsequently, we tested the hypothesis that firn
is the mediator of flo non-cell autonomy by examining fim expression in flo
periclinal chimeras. In these chimeras, firn is activated in cells where f
lo is not expressed, indicating that firn cannot be the sole mediator of fl
o non-cell autonomy.