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病毒感染与细胞周期G2/M调控

Viral infections and cell cycle G2/M regulation.

作者信息

Zhao Richard Y, Elder Robert T

机构信息

Department of Pathology, University of Maryland School of Medicine, Baltimore, MD 2120, USA.

出版信息

Cell Res. 2005 Mar;15(3):143-9. doi: 10.1038/sj.cr.7290279.

Abstract

Progression of cells from G2 phase of the cell cycle to mitosis is a tightly regulated cellular process that requires activation of the Cdc2 kinase, which determines onset of mitosis in all eukaryotic cells. In both human and fission yeast (Schizosaccharomyces pombe) cells, the activity of Cdc2 is regulated in part by the phosphorylation status of tyrosine 15 (Tyr15) on Cdc2, which is phosphorylated by Wee1 kinase during late G2 and is rapidly dephosphorylated by the Cdc25 tyrosine phosphatase to trigger entry into mitosis. These Cdc2 regulators are the downstream targets of two well-characterized G2/M checkpoint pathways which prevent cells from entering mitosis when cellular DNA is damaged or when DNA replication is inhibited. Increasing evidence suggests that Cdc2 is also commonly targeted by viral proteins, which modulate host cell cycle machinery to benefit viral survival or replication. In this review, we describe the effect of viral protein R (Vpr) encoded by human immunodeficiency virus type 1 (HIV-1) on cell cycle G2/M regulation. Based on our current knowledge about this viral effect, we hypothesize that Vpr induces cell cycle G2 arrest through a mechanism that is to some extent different from the classic G2/M checkpoints. One the unique features distinguishing Vpr-induced G2 arrest from the classic checkpoints is the role of phosphatase 2A (PP2A) in Vpr-induced G2 arrest. Interestingly, PP2A is targeted by a number of other viral proteins including SV40 small T antigen, polyomavirus T antigen, HTLV Tax and adenovirus E4orf4. Thus an in-depth understanding of the molecular mechanisms underlying Vpr-induced G2 arrest will provide additional insights into the basic biology of cell cycle G2/M regulation and into the biological significance of this effect during host-pathogen interactions.

摘要

细胞从细胞周期的G2期进入有丝分裂是一个受到严格调控的细胞过程,该过程需要激活Cdc2激酶,Cdc2激酶决定了所有真核细胞中有丝分裂的起始。在人类细胞和裂殖酵母(粟酒裂殖酵母)细胞中,Cdc2的活性部分受其酪氨酸15(Tyr15)磷酸化状态的调节,在G2晚期,Wee1激酶会使Tyr15磷酸化,而Cdc25酪氨酸磷酸酶会迅速使其去磷酸化,从而触发细胞进入有丝分裂。这些Cdc2调节因子是两条特征明确的G2/M检查点途径的下游靶点,当细胞DNA受损或DNA复制受到抑制时,这两条途径会阻止细胞进入有丝分裂。越来越多的证据表明,Cdc2也是病毒蛋白的常见靶点,病毒蛋白会调节宿主细胞周期机制,以利于病毒的存活或复制。在本综述中,我们描述了1型人类免疫缺陷病毒(HIV-1)编码的病毒蛋白R(Vpr)对细胞周期G2/M调节的影响。基于我们目前对这种病毒效应的了解,我们假设Vpr通过一种在某种程度上不同于经典G2/M检查点的机制诱导细胞周期G2期阻滞。Vpr诱导的G2期阻滞与经典检查点的一个独特区别在于磷酸酶2A(PP2A)在Vpr诱导的G2期阻滞中的作用。有趣的是,PP2A也是许多其他病毒蛋白的靶点,包括SV40小T抗原、多瘤病毒T抗原、HTLV Tax和腺病毒E4orf4。因此,深入了解Vpr诱导G2期阻滞的分子机制,将为细胞周期G2/M调节的基础生物学以及宿主-病原体相互作用期间这种效应的生物学意义提供更多见解。

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