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Publication : Identification of CDK4 as a target of c-MYC.

First Author  Hermeking H Year  2000
Journal  Proc Natl Acad Sci U S A Volume  97
Issue  5 Pages  2229-34
PubMed ID  10688915 Mgi Jnum  J:60924
Mgi Id  MGI:1354092 Doi  10.1073/pnas.050586197
Citation  Hermeking H, et al. (2000) Identification of CDK4 as a target of c-MYC. Proc Natl Acad Sci U S A 97(5):2229-34
abstractText  The prototypic oncogene c-MYC encodes a transcription factor that can drive proliferation by promoting cell-cycle reentry. However, the mechanisms through which c-MYC achieves these effects have been unclear. Using serial analysis of gene expression, we have identified the cyclin-dependent kinase 4 (CDK4) gene as a transcriptional target of c-MYC. c-MYC induced a rapid increase in CDK4 mRNA levels through four highly conserved c-MYC binding sites within the CDK4 promoter. Cell-cycle progression is delayed in c-MYC-deficient RAT1 cells, and this delay was associated with a defect in CDK4 induction. Ectopic expression of CDK4 in these cells partially alleviated the growth defect. Thus, CDK4 provides a direct link between the oncogenic effects of c-MYC and cell-cycle regulation.
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