生物
E2F型
SKP2型
基因敲除
异位表达
癌症研究
细胞周期
E2F1
癌变
基因
基因表达
转染
分子生物学
遗传学
泛素连接酶
泛素
出处
期刊:Oncogene
[Springer Nature]
日期:2005-12-05
卷期号:25 (18): 2615-2627
被引量:115
标识
DOI:10.1038/sj.onc.1209286
摘要
The F-box-containing protein Skp2 plays a critical role in coordinating the G1/S transition and progression through the S phase of the mammalian cell cycle. Skp2 is overexpressed in a broad spectrum of human cancers and the expression level correlates with tumor malignancy. However, the Skp2 gene is neither amplified nor rearranged in most human cancers and the underlying mechanism of Skp2 overexpression remains poorly understood. We show here that the Skp2 gene contains a functional E2F response element (hSRE2). Ectopic expression of E2F1 induces expression of the endogenous Skp2 gene in human fibroblast cells, whereas antisense-mediated knockdown of E2F1 in human tumor cell lines reduces expression of endogenous Skp2 gene. The hSRE2 element not only participates in activation of Skp2 promoter function during normal cell cycle progression into S phase, it is also required for the high-level Skp2 gene expression in many human tumor cell lines. These results reveal Skp2 as a novel target for E2F regulation that is disrupted in several human tumor cell lines.
科研通智能强力驱动
Strongly Powered by AbleSci AI