B-Myb belongs to a family of related transcription factors which share
a unique DNA binding domain. B-Myb plays an important role in regulat
ion of the cell cycle. Its expression is upregulated by the human papi
lloma virus HPV16 E7 oncoprotein. Overexpression of B-Myb can bypass p
53-mediated cell cycle arrest. The founding member of the myb gene fam
ily, c-Myb, and A-Myb are involved in hematopoiesis and neurogenesis,
respectively, and are both activators of gene transcription. Whether B
-Myb is a transactivator or a repressor, however, has remained a matte
r of discussion. We reviewed the transactivation potential of B-Myb in
yeast, taking advantage of the fact that inducible gene activation is
an evolutionarily conserved process. By mutational analysis we locali
zed a conserved activation domain in B-Myb. In vertebrate cells the tr
ansactivation potential of B-Myb is concealed by the C-terminal part o
f the protein. We show that the cell cycle regulators cyclin A and cyc
lin E activate B-Myb by eradicating the inhibition mediated by its car
boxy-terminus. Our data suggest that in vertebrates the trans-activati
ng function of B-Myb is regulated during the cell cycle and link Myb f
unctions to cell cycle progression.