CAC1 negatively regulates RARα activity through cooperation with HDAC

Retinoic acid (RA) plays pleiotropic roles in cellular differentiation and animal development. RA responses are mediated by transcriptional activation by the retinoic acid receptor (RAR) and retinoid X receptor (RXR) in cooperation with various types of coregulators at RA-responsive gene promoters. Here, we identified CDK2-associated cullin (CAC1) as a novel type of RARα coregulator that interacts with RARα and inhibits its transcriptional activity. The CoRNR box of CAC1 is required for the binding to and inactivation of RARα. In addition, CAC1 cooperates with histone deacetylases (HDACs) to suppress RARα, probably by associating with HDAC. Finally, depletion of CAC1 increases RA-induced neuronal differentiation of P19 cells, a response accompanied by significant upregulation of the neuronal marker nestin. From these results, we suggest that CAC1 is a novel corepressor of RARα that cooperates with HDACs and is involved in the regulation of RA-induced cellular differentiation.

► The newly identified protein CAC1 interacts with RARα through conserved CoRNR box.
► This interaction leads to repression of the transcriptional activity of RARα.
► HDAC cooperates with CAC1 for RARα repression.
► CAC1 negatively regulates RA-induced neuronal differentiation of P19 cells.