IDENTIFICATION OF PROTEINS THAT INTERACT WITH CREB DURING DIFFERENTIATION OF F9 EMBRYONAL CARCINOMA-CELLS

The mammalian transcription factor CREB is thought to activate cAMP-inducible genes in a variety of differentiated cell types and is probably involved in other signalling pathways. Undifferentiated F9 embryonal carcinoma (UF9) cells are refractory to cAMP and become cAMP-responsive following differentiation to endoderm like cells. It has been proposed that UF9 cells contain a negative regulator(s) of the cAMP-response that might act through direct interaction with CREB. We have used a protein blotting assay and P-32-labelled CREB to probe for CREB-binding proteins in nuclear extracts from F9 cells and to examine their abundance during differentiation. We find that ATF1 (a protein that is highly homologous to CREB) and a novel polypeptide(s) of approximately 100 kDa (CBP100) are the major CREB-binding proteins in extracts from UF9 cells. As expected ATF1 is detected due to leucine zipper-dependent heterodimerisation with CREB. In contrast CBP100 interacts with CREB independently of the leucine zipper. The total amount of ATF1 and the amount of ATF1 that is complexed with CREB are substantially reduced following differentiation. In addition, ATF1 mRNA levels are lower in differentiated F9 cells indicating that a pretranslational mechanism contributes to the decreased ATF1 protein levels observed. CBP100 levels are also reduced or CBP100 is modified upon differentiation. We discuss the potential roles of ATF1 and CBP100 in regulating CREB activity during differentiation of F9 embryonal carcinoma cells.