Two groups of genes, the Polycomb group (Pc-G) and trithorax group (tr
x-G), have been identified in Drosophila to provide a transcriptional
memory mechanism. They ensure the maintenance of transcription pattern
s of key regulators such as the Hox genes and thereby the correct exec
ution of developmental programmes. Recent data suggest that this memor
y mechanism is conserved in vertebrates and plants. Here we discuss cu
rrent insights into the role of mouse Pc-G genes, with a particular fo
cus on the best-studied Bmi1, Mel18 and M33 genes, as representative e
xamples. Common phenotypes observed in knockout mice mutant for each o
f these genes indicate an important role for Pc-G genes not only in re
gulation of Hox gene expression and axial skeleton development but als
o in control of proliferation and survival of haematopoietic cell line
ages. Proliferation defects are also observed in other cell lineages d
erived from these null-mutant mice, and provide new tools to study the
impact of Pc-G deregulation on cell cycle control.