MADS-box genes encode transcription factors in all eukaryotic organisms thu
s far studied. Plant MADS-box proteins contain a DNA-binding (M), an interv
ening (I), a Keratin-like (K) and a C-terminal C-domain, thus plant MADS-bo
x proteins are of the MIKC type. In higher plants most of the well-characte
rized genes are involved in floral development. They control the transition
from vegetative to generative growth and determine inflorescence meristem
identity. They specify floral organ identity as outlined in the ABC model o
f floral development. Moreover, in Antirrhinum majus the MADS-box gene prod
ucts DEF/GLO and PLE control cell proliferation in the developing flower bu
d. In this species the DEF/GLO and the SQUA proteins form a ternary complex
which determines the overall "Bauplan" of the flower.
Phylogenetic reconstructions of MADS-box sequences obtained from ferns, gym
nosperms and higher eudicots reveal that, although ferns possess already MI
KC type genes, these are not orthologous to the well characterized MADS-box
genes from gymnosperms or angiosperms. Putative orthologs of floral homeot
ic B- and C-function genes: have been identified in different gymnosperms s
uggesting that these genes evolved some 300-400 million years ago. Both gym
nosperms and angiosperms also contain a hitherto unknown sister clade of th
e B-genes, which we termed Bsister. A novel hypothesis will be described su
ggesting that B and Bsister might be involved in sex determination of male
and female reproductive organs, respectively.