RELIEF OF YY1-INDUCED TRANSCRIPTIONAL REPRESSION BY PROTEIN-PROTEIN INTERACTION WITH THE NUCLEOLAR PHOSPHOPROTEIN B23

Previous studies have shown that the transcription factor YY1 can both activate and repress transcription of many mammalian genes (reviewed by Hahn (Hahn, S. (1992) Curr. Biol. 2, 152-154)). Given the diverse e ffects of the YY1 protein, it seems likely that its function depends o n interaction with other cellular factors. We have used the yeast two- hybrid system to isolate mouse cDNAs encoding proteins capable of dire ctly binding to YY1. Sequence analysis of one clone revealed it had an open reading frame with the potential to code for a protein nearly id entical to the previously published mouse nucleolar phosphoprotein B23 . The YY1.B23 complex is specific, and occurs in vivo and in vitro. Ov erexpression of the B23 protein can reverse the transcriptional repres sion exerted by YY1. These results suggest a role for a nucleolar prot ein as a component in transcription and provide a possible mechanism f or transcriptional regulation by YY1.