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小鼠细胞周期蛋白E基因的细胞周期调控取决于启动子中的一个E2F结合位点。

Cell cycle regulation of the murine cyclin E gene depends on an E2F binding site in the promoter.

作者信息

Botz J, Zerfass-Thome K, Spitkovsky D, Delius H, Vogt B, Eilers M, Hatzigeorgiou A, Jansen-Dürr P

机构信息

Forschungsschwerpunkt Angewandte Tumorvirologie,Deutsches Krebsforschungszentrum für Molekulare Biologie der Universität, Heidelberg, Germany.

出版信息

Mol Cell Biol. 1996 Jul;16(7):3401-9. doi: 10.1128/MCB.16.7.3401.

Abstract

Cyclin E controls progression through the G1 phase of the cell cycle in mammalian fibroblasts and potentially in many other cell types. Cyclin E is a rate-limiting activator of cdk2 kinase in late G1. The abundance of cyclin E is controlled by phase-specific fluctuations in the mRNA level; in mammalian fibroblasts, mRNA is not detected under conditions of serum starvation and is accumulated upon serum stimulation, with expression starting in mid-G1. Here, we report the cloning of the murine cyclin E promoter. We isolated a 3.8-kb genomic fragment that contains several transcriptional start sites and confers cell cycle regulation on a luciferase reporter gene. This fragment also supports transcriptional activation by adenovirus E1A, a known upstream regulator of cyclin E gene expression. An E2F binding site which is required for G1-specific activation of the cyclin E promoter in synchronized NIH 3T3 cells was identified in this fragment.

摘要

细胞周期蛋白E控制哺乳动物成纤维细胞以及可能许多其他细胞类型中细胞周期G1期的进程。细胞周期蛋白E是G1晚期cdk2激酶的限速激活剂。细胞周期蛋白E的丰度受mRNA水平的阶段特异性波动控制;在哺乳动物成纤维细胞中,血清饥饿条件下检测不到mRNA,血清刺激后mRNA积累,表达始于G1中期。在此,我们报道了小鼠细胞周期蛋白E启动子的克隆。我们分离出一个3.8 kb的基因组片段,该片段包含几个转录起始位点,并赋予荧光素酶报告基因细胞周期调控能力。该片段还支持腺病毒E1A的转录激活,E1A是细胞周期蛋白E基因表达的已知上游调节因子。在该片段中鉴定出了同步化的NIH 3T3细胞中细胞周期蛋白E启动子G1特异性激活所需的E2F结合位点。

相似文献

2
Regulation of the cyclin E gene by transcription factor E2F1.转录因子E2F1对细胞周期蛋白E基因的调控。
Proc Natl Acad Sci U S A. 1995 Dec 19;92(26):12146-50. doi: 10.1073/pnas.92.26.12146.

引用本文的文献

本文引用的文献

1
Regulation of the cyclin E gene by transcription factor E2F1.转录因子E2F1对细胞周期蛋白E基因的调控。
Proc Natl Acad Sci U S A. 1995 Dec 19;92(26):12146-50. doi: 10.1073/pnas.92.26.12146.

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