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J Biol Chem, Vol. 273, Issue 35, 22563-22569, August 28, 1998
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From the Both BTG1 and BTG2 are
involved in cell-growth control. BTG2 expression is
regulated by p53, and its inactivation in embryonic stem cells leads to
the disruption of DNA damage-induced G2/M cell-cycle
arrest. In order to investigate the mechanism underlying Btg-mediated
functions, we looked for possible functional partners of Btg1 and Btg2.
Using yeast two-hybrid screening, protein-binding assays, and transient
transfection assays in HeLa cells, we demonstrated the physical
in vitro and in vivo interaction of both Btg1
and Btg2 with the mouse protein mCaf1 (i.e. mouse
CCR4-associated factor 1).
mCaf1 was identified through its interaction with the CCR4 protein, a
component of a general transcription multisubunit complex, which, in
yeast, regulates the expression of different genes involved in
cell-cycle regulation and progression. These data suggest that Btg
proteins, through their association with mCaf1, may participate, either
directly or indirectly, in the transcriptional regulation of the genes
involved in the control of the cell cycle. Finally, we found that box
B, one of two conserved domains which define the Btg family, plays a
functional role, namely that it is essential to the Btg-mCaf1
interaction.
Unité INSERM U453, Centre Léon
Bérard, 69373 Lyon Cedex 08, France, the

Laboratoire de Cytogénétique
Moléculaire, Hôpital Edouard Herriot, 69373 Lyon Cedex 03, France, and the ** Laboratoire de Génétique, UMR 5641 CNRS,
Domaine Rockefeller, Université Claude Bernard,
Lyon 1, France
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