We have investigated the effect of the v-Myc oncoprotein on gene expression in myelomonocytic cells. We find that v-Myc dramatically down-regulates the expression of myelomonocytic-specific genes, such as the chicken mim-1 and lysozyme genes, both of which are known targets for C/EBP transcription factors. We present evidence that Myc downregulates these genes by inhibiting the function of C/EBP transcription factors. Detailed examination of the inhibitory mechanism shows that amino-terminal sequences of v-Myc, but not its DNA-binding domain, are required for the suppression of C/EBP-dependent transactivation. Our findings identify a new function for Myc and reveal a novel mechanism by which Myc affects the expression of other genes.Numerous studies have implicated the c-myc gene in a variety of cellular processes, such as proliferation, differentiation, and apoptosis, and have shown that mutant forms of the gene, such as transduced (v-myc) or rearranged myc alleles, are involved in tumorigenesis (1-6). It is now widely believed that c-myc plays a central role in a switch mechanism by which normal cells decide between the alternative fates of proliferation, differentiation, and apoptosis and that deregulation of c-myc causes an imbalance in this switch mechanism, resulting in the development of neoplasia.Structural and functional analyses have identified the c-myc protein product (c-Myc) as a transcription factor. The carboxyl terminus of c-Myc forms a basic region-helix-loop-helixleucine zipper (B-HLH-LZ) DNA-binding domain, heterodimerizes with the Max protein (7), and recognizes the consensus Myc binding site, CACGTG (8-10), whereas the amino terminus of c-Myc functions as a transcriptional activation domain (11)(12)(13)(14). Several genes whose expression is induced by c-Myc have been identified (15)(16)(17)(18)(19)(20). In addition, c-Myc also inhibits gene expression. The C/EBPa gene (21,22) and the adenovirus-2 major late promoter (22, 23) are downregulated by c-Myc. Interestingly, repression of these genes does not depend on Myc-specific DNA-binding sites but is mediated by so-called initiator elements located in the promoters of these genes (22, 23). Thus, increasing evidence suggests that c-Myc affects gene expression by several different mechanisms. Nevertheless, an unambiguous functional relationship to the physiological or malignant activities of myc has not been established for any of the putative target genes identified so far.We have studied the effect of v-Myc on gene expression in myelomonocytic cells. We have found that v-Myc inhibits the expression of several genes, including mim-1 and the lysozyme gene, both of which have been shown to be targets for C/EBP transcription factors (24,25). We have analyzed the mechanism by which Myc down-regulates these genes and have found that amino-terminal sequences of Myc interfere with the function of C/EBP transcription factors. Our findings identify a novel function for Myc and reveal a novel mechanism by which Myc affects the expression of othe...