In Drosophila and mouse, Polycomb group genes are involved in the main
tenance of homeotic gene expression patterns throughout development. H
ere we report the skeletal phenotypes of compound mutants for two Poly
comb group genes bmi1 and M33. We show that mice deficient for both bm
i1 and M33 present stronger homeotic transformations of the axial skel
eton as compared to each single Polycomb group mutant, indicating stro
ng dosage interactions between those two genes. These skeletal transfo
rmations are accompanied with an enhanced shift of the anterior limit
of expression of several Hox genes in the semitic mesoderm. Our result
s demonstrate that in mice the Polycomb group genes act in synergy to
control the nested expression pattern of some Hox genes in semitic mes
odermal tissues during development.