| Literature DB >> 7957050 |
Abstract
Through a PCR-based differential screening method, cyclin G was identified as a novel transcriptional target of the p53 tumor suppressor gene product. In both a mouse p53 temperature-sensitive leukemic cell line and mouse embryonic fibroblasts (MEF) after gamma-irradiation, cyclin G mRNA was rapidly induced. MEF from a p53-deficient mouse expressed cyclin G at a level > 10-fold lower than that from a wild-type mouse. Using a DNA binding assay, a specific p53 binding site was identified upstream from the cyclin G gene, which functioned as a p53-dependent cis-acting element in a transient transfection assay. These results suggest that cyclin G might participate in a p53-mediated pathway to prevent tumorigenesis.Entities:
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Year: 1994 PMID: 7957050 PMCID: PMC395420 DOI: 10.1002/j.1460-2075.1994.tb06807.x
Source DB: PubMed Journal: EMBO J ISSN: 0261-4189 Impact factor: 11.598