PIP, A NOVEL IRF FAMILY MEMBER, IS A LYMPHOID-SPECIFIC, PU.1-DEPENDENT TRANSCRIPTIONAL ACTIVATOR

The immunoglobulin light-chain gene enhancers E(kappa 3), E(lambda 2-4 ), and E(lambda 3-1) contain a conserved cell type-specific composite element essential for their activities. This element binds a B cell-sp ecific heterodimeric protein complex that consists of the Ets family m ember PU.1 and a second factor (NF-EM5), whose participation in the fo rmation of the complex is dependent on the presence of DNA-bound PU.1. In this report we describe the cloning and characterization of Pip (P U.1 interaction partner), a lymphoid-specific protein that is most lik ely NF-EM5. As expected, the Pip protein binds the composite element o nly in the presence of PU.1; furthermore, the formation of this ternar y complex is critically dependent on phosphorylation of PU.1 at serine -148. The Pip gene is expressed specifically in lymphoid tissues in bo th B- and T-cell lines. When coexpressed in NIH-3T3 cells, Pip and PU. 1 function as mutually dependent transcription activators of the compo site element. The amino-terminal DNA-binding domain of Pip exhibits a high degree of homology to the DNA-binding domains of members of the i nterferon regulatory factor (IRF) family, which includes IRE-1, IRF-2, ICSBP, and ISGF3 gamma.