Journal
MOLECULAR AND CELLULAR BIOLOGY
Volume 21, Issue 11, Pages 3789-3806Publisher
AMER SOC MICROBIOLOGY
DOI: 10.1128/MCB.21.11.3789-3806.2001
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Funding
- NHLBI NIH HHS [R01 HL056745, HL56745] Funding Source: Medline
- NIDDK NIH HHS [F32 DK009892, F32DK09892] Funding Source: Medline
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CCAAT/enhancer binding protein alpha (C/EBP alpha) is an integral factor in the granulocytic developmental pathway, as myeloblasts from C/EBP alpha -null mice exhibit an early block in differentiation. Since mice deficient for known C/EBP alpha target genes do not exhibit the same block in granulocyte maturation, we sought to identify additional C/EBP alpha target genes essential for myeloid cell development. To identify such genes, we used both representational difference analysis and oligonucleotide array analysis with RNA derived from a C/EBP alpha -inducible myeloid cell line. From each of these independent screens, we identified c-Myc as a C/EBP alpha negatively regulated gene. We mapped an E2F binding site in the c-Myc promoter as the cis-acting element critical for C/EBP alpha negative regulation. The identification of c-Myc as a C/EBP alpha target gene is intriguing, as it has been previously shown that down-regulation of c-Myc can induce myeloid differentiation. Here we show that stable expression of c-Myc from an exogenous promoter not responsive to C/EBP alpha -mediated down-regulation forces myeloblasts to remain in an undifferentiated state. Therefore, C/EBP alpha negative regulation of c-Myc is critical for allowing early myeloid precursors to enter a differentiation pathway. This is the first report to demonstrate that C/EBP alpha directly affects the level of c-Myc expression and, thus, the decision of myeloid blasts to enter into the granulocytic differentiation pathway.
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