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E2F靶基因与细胞周期检查点控制。

E2F target genes and cell-cycle checkpoint control.

作者信息

Lavia P, Jansen-Dürr P

机构信息

Centro di Genetica Evoluzionistica C.N.R., c/o Universita La Sapienza, Rome, Italy.

出版信息

Bioessays. 1999 Mar;21(3):221-30. doi: 10.1002/(SICI)1521-1878(199903)21:3<221::AID-BIES6>3.0.CO;2-J.

Abstract

In this review, we will focus on the role played by transcription factors of the E2F/DP family in controlling the expression of genes that carry out important cell-cycle control functions, thereby ensuring ordered progression through the mammalian cell division cycle. The emerging picture is that cell-cycle progression depends on the execution of a regulatory cascade of gene expression, driven by E2F/DP transcription factors, which are in turn regulated by the products of some of these genes. That E2F factors are potent regulators of cell-cycle checkpoints in mammalian cells is supported by experiments demonstrating that ectopic expression of individual E2F family members is sufficient to modulate cell proliferation and apoptosis. It is also clear that deregulation of E2F activity will result in the loss of particular checkpoint controls, thereby predisposing cells to malignant conversion.

摘要

在本综述中,我们将聚焦于E2F/DP家族转录因子在控制执行重要细胞周期调控功能的基因表达中所起的作用,从而确保哺乳动物细胞分裂周期有序进行。新出现的情况是,细胞周期进程依赖于由E2F/DP转录因子驱动的基因表达调控级联反应的执行,而这些转录因子又受到其中一些基因产物的调控。实验表明,单个E2F家族成员的异位表达足以调节细胞增殖和凋亡,这支持了E2F因子是哺乳动物细胞中细胞周期检查点的有效调节因子这一观点。同样清楚的是,E2F活性的失调将导致特定检查点控制的丧失,从而使细胞易于发生恶性转化。

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