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E2F转录因子对Geminin和Cdt1表达的调控。

Regulation of Geminin and Cdt1 expression by E2F transcription factors.

作者信息

Yoshida Kenichi, Inoue Ituro

机构信息

Genetic Diagnosis, Institute of Medical Science, University of Tokyo, 4-6-1 Shirokanedai, Minato-ku, Tokyo 108-8639, Japan.

出版信息

Oncogene. 2004 May 6;23(21):3802-12. doi: 10.1038/sj.onc.1207488.

Abstract

Geminin and Cdt1 play an essential role in the initiation of DNA replication, by regulating the chromatin loading of the MCM complex. In this study, we showed that the transcription of human Geminin and Cdt1, as well as that of MCM7, is activated by transcription factors E2F1-4, but not by factors E2F5-7. Analysis of various Geminin and Cdt1 promoter constructs showed that an E2F-responsive sequence in the vicinity of the transcription initiation site is necessary for the transcriptional activation. The promoter activity for human Geminin was activated by the E7, but not E6, oncogene of human papillomavirus type 16. While E2F1-induced activation of human Cdt1 gene transcription was suppressed by pRb, but not by p107 or p130, its E2F4-induced activation was suppressed by pRb, p107, and p130. Furthermore, the promoter activities of human Geminin and Cdt1 were demonstrated to be growth-dependent. Taken together, the results demonstrate that Geminin and Cdt1 constitute targets for various members of the E2F family of transcription factors, and that expression of Geminin and Cdt1 is perhaps mediated by the activation of a pRb/E2F pathway.

摘要

Geminin和Cdt1通过调节MCM复合物的染色质加载,在DNA复制起始过程中发挥重要作用。在本研究中,我们发现人类Geminin和Cdt1以及MCM7的转录由转录因子E2F1 - 4激活,而非E2F5 - 7。对各种Geminin和Cdt1启动子构建体的分析表明,转录起始位点附近的E2F反应序列对于转录激活是必需的。人乳头瘤病毒16型的E7癌基因可激活人类Geminin的启动子活性,而E6则不能。虽然E2F1诱导的人类Cdt1基因转录激活被pRb抑制,而非p107或p130,但E2F4诱导的激活被pRb、p107和p130抑制。此外,人类Geminin和Cdt1的启动子活性被证明与生长相关。综上所述,结果表明Geminin和Cdt1是E2F转录因子家族各成员的作用靶点,并且Geminin和Cdt1的表达可能由pRb/E2F途径的激活介导。

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