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ABSTRACTcDNAs representing the a subunit of polyomavirus enhancer binding protein 2 (PEBP2; also cafled PEA2) were isolated. The products of the cDNAs are highly homologous to that of Drosophila segmentation gene runt (run) for an N-proximal 128-amino acid region showing 66% identity. The run homology region encompasses the domain capable of binding to a specific nucleotide sequence motif and of dimerizing with the companion 13 subunit. The human AMLI gene related to t(8;21) acute myeloid leukemia also has a run homology region. Together with the 18 subunit, which increases the affinity of the a subunit to DNA without binding to DNA by itself, PEBP2 represents a newly discovered family of transcription factor. The major species of PEBP2a mRNA was expressed in T-cell lines but not in B-cell lines tested. Evidence indicated that PEBP2 functions as a transcriptional activator and is,involved in regulation of T-ceil-specific gene expression.Potential use of polyomavirus (Py) as a probe of mouse development has been recognized since it was observed that the wild-type Py did not grow in embryonal carcinoma cells but that it grew when the cells were induced to differentiate (1)(2)(3)(4)(5). Through the analysis of the Py enhancer, which determines the differentiation-dependent and cell-typespecific expression of the viral genes, a number of transcription factors involved in developmental regulation have been identified (6-10).PEBP2/PEA2, which binds to both the A and B cores of the Py enhancer (11), is undetectable in embryonal carcinoma F9 cells and becomes detectable after the cells are induced to differentiate (6,7). It specifically recognizes a consensus sequence, R/TACCRCA (R, purine), which was originally identified in the Py enhancer (11) and is also compatible with the core motif of murine leukemia virus enhancers (12,13). In addition, many T-cell-specific genes, such as T-cell receptor (TCR) a, X3, yand 8 and CD3e genes, contain potential PEBP2 binding sites, suggesting the possibility that PEBP2 is involved in T-cell-specific gene expression (13 [708][709][710][711][712][713][714]. The mutations are the same as the M2 mutation (14). For expression in mammalian cells, the coding regions of al, a2, and 831 cDNAs were cloned into the Xho I site of pCDMPy, in which the Py origin and enhancer region were deleted from pCDM8 (Invitrogen), resulting in pCDMPy-al, pCDMPy-a2, and pCDMPy-31. The bacterial expression plasmids pETal and pETa2, carrying the whole coding regions of al and a2 cDNAs, were constructed in the same way as pETf82 (16). To produce deletion mutants of a2, the whole coding region of a2 cDNA was inserted into the BamHI/HindIII fragment of plasmid pQE9 (Qiagen) resulting in pQE9-a2 encoding a fusion protein tagged with an N-terminal histidine cluster. Various deletions were introduced into pQE9-a2 using appropriate restriction sites: N94C306 encodes a region of aa 94-306; N1C226 encodes aa 1-226; N1C158 encodes aa 1-158; N80C226 encodes aa 80-226. N1C226, N1C158, and N80C226 proteins have one, two, o...

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A murine transcription factor, PEBP2, is composed of two subunits, a and ,B. There are two genes in the mouse genome, PEBP2aA and PEBP2&aB, which encode the at subunit. Two types of the aLB cDNA clones, aLBi and aB2, were isolated from mouse fibroblasts and characterized. They were found to represent 3.8-and 7.9-kb transcripts, respectively. The 3.8-kb RNA encodes the previously described aB protein referred to as oiBl, while the 7.9-kb RNA encodes a 387-amino-acid protein, termed aB2, which is identical to aBl except that it has an internal deletion of 64 amino acid residues. Both otBl and aB2 associate with PEBP2,I and form a heterodimer. The atB2/4 complex binds to the PEBP2 binding site two-to threefold more strongly than the aB1/,I complex does. aBl stimulates transcription through the PEBP2 site about 40-fold, while aB2 is only about 25 to 45% as active as aBl. Transactivation domain is located downstream of the 128-amino-acid runt homology region, referred to as the Runt domain. Mouse chromosome mapping studies revealed that aA, aB, and ,B genes are mapped to chromosomes 17, 16, and 8, respectively. The last two genes are syntenic with the human AMLI on chromosome 21q22 and PEBP24/CBFD on 16q22 detected at the breakpoints of characteristic chromosome translocations of the two different subtypes of acute myeloid leukemia. These results suggest that the previously described chimeric gene products, AML1/MTG8(ETO) and AMLl-EAP generated by t(8;21) and t(3;21), respectively, lack the transactivation domain of AMLL.A murine transcription factor, PEBP2, also called PEA2, was identified as a factor which binds to the region of the polyomavirus enhancer originally termed the PEA2 site (35). PEBP2 functionally cooperates with other enhancer corebinding proteins, including AP1 and Ets family proteins, PEA3 (48), , and PEBP5 (2), and plays an important role in stimulation of transcription and viral DNA replication. PEBP2 is composed of a and 3 subunits (32, 34). The at subunit bind to DNA by recognizing the consensus sequence, (Pu/T) ACCPuCA (13,34). The companion 3 subunit binds to the cx protein and increases the affinity of the a protein to DNA without binding to DNA by itself (32). cDNAs coding for both subunits have been cloned and characterized in detail (32, 34).PEBP2 has recently been shown to be closely related to acute myeloid leukemia (AML). The t(8;21)(q22;q22) translocation is one of the most frequent chromosome abnormalities in AML and is classified into the FAB-M2 subtype of AML (39). It has been shown that the t(8;21) breakpoints in the chromosome 21 are clustered in the recently described AMLI gene (27), the product of which shares a high homology within the 128-amino-acid (aa) region with the product of the Drosophila segmentation gene, runt (14), and the at subunit of PEBP2 (8,9,34 genome, oaB, which shares a high sequence homology with the original ao gene, termed aA. The aB gene as a whole is highly homologous to human AMLl (3). The discovery of the homology of the AML1 protein to the otsubunit o...