Proceedings of the National Academy of Sciences · 1988 · 184 citations · 40 references
Life SciencesCell BiologyGeneticsCell DifferentiationGene ExpressionGene RegulationCell Differentiation ControlHematopoietic DifferentiationMyc Family OncogenesOncogene ActivationTranscription Factor OncogenesTranscriptional Regulation In EukaryotesC-myc RegulationErythroid Lineage CommitmentFos OncogenesMyc Transcriptional ActivationOncogene RegulationTranscriptional ActivationTranscripts
The role of nuclear protooncogenes during erythroid cell differentiation was examined by transfecting exogenous c-fos and c-myb genes into mouse erythroleukemia cells, which can be induced to differentiate either with erythropoietin (Epo) or dimethyl sulfoxide. Expression of exogenous c-myb or c-fos oncogene completely inhibited Epo-induced erythroid differentiation but only partially inhibited dimethyl sulfoxide-induced differentiation. Normally Epo-induced differentiation leads to a drastic decline of c-myb mRNA levels and an increase of c-myc transcripts in the early stage of differentiation. Cells expressing exogenous c-fos gene, however, maintained high levels of c-myb mRNA after Epo treatment. This high level of c-myb transcripts was found to be due to block of transcription shutoff (or transcriptional activation) rather than to mRNA stabilization. It is concluded that the down-regulation of endogenous c-myb gene expression is a prerequisite for commitment of Epo-induced erythroid differentiation and that expression of c-myb gene may be indirectly regulated by c-fos gene product. We also concluded that early down-regulation of c-myc gene expression is not essential for erythroid differentiation and that gene regulation of chemically induced erythroid differentiation may differ from that of Epo-induced differentiation.
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Stimulation of 3T3 cells induces transcription of the c-fos proto-oncogene
Michael E. Greenberg, Edward B. Ziff · Nature · 1984 · 3.2K citations