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首页> 外文期刊>Molecular Immunology >Transactivators Zta and Rta of Epstein-Barr virus promote G0/G1 to S transition in Raji cells: a novel relationship between lytic virus and cell cycle.
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Transactivators Zta and Rta of Epstein-Barr virus promote G0/G1 to S transition in Raji cells: a novel relationship between lytic virus and cell cycle.

机译:Epstein-Barr病毒的反式激活因子Zta和Rta促进Raji细胞中G0 / G1向S的转变:裂解病毒和细胞周期之间的新关系。

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In the present study, we show that the treatment of Epstein-Barr virus (EBV) latently infected Raji cells with TPA/SB caused the cell growth arrest. The Zta-positive cells were predominantly enriched in G0/G1 phase of cell cycle. When Zta expression reached a maximal level, a fraction of Zta expressing cell population reentered S phase. Analysis of the expression pattern of a key set of cell cycle regulators revealed that the expression of Zta and Rta substantially interfered with the cell cycle regulatory machinery in Raji cells, strongly inhibiting the expression of Rb and p53 and inducing the expression of E2F1. Down-regulation of Rb was further demonstrated to be mediated by proteasomal degradation, and p53 and p21 affected at transcription level. The data indicate that both Zta and Rta promote entry into S phase of Raji cells. The important roles of Zta and Rta in EBV lytic reactivation were also demonstrated. Our finding suggests that these two transcriptional activators may act synergistically to govern the expression of downstream early and late genes as well as cellular genes and initiation of lytic cycle and manipulation of cell cycle regulatory mechanisms require the joint and interactive contributions of Rta and Zta.
机译:在本研究中,我们表明用TPA / SB处理爱泼斯坦-巴尔病毒(EBV)潜在感染的Raji细胞会导致细胞生长停滞。 Zta阳性细胞主要富集于细胞周期的G0 / G1期。当Zta表达达到最大水平时,一部分表达Zta的细胞群体重新进入S期。对一组关键的细胞周期调节因子的表达模式的分析表明,Zta和Rta的表达实质上干扰了Raji细胞的细胞周期调节机制,强烈抑制了Rb和p53的表达并诱导E2F1的表达。 Rb的下调被进一步证明是由蛋白酶体降解介导的,并且p53和p21在转录水平受到影响。数据表明Zta和Rta都促进Raji细胞进入S期。还证明了Zta和Rta在EBV裂解激活中的重要作用。我们的发现表明,这两种转录激活因子可能协同作用来控制下游早期和晚期基因以及细胞基因的表达,裂解周期的启动和细胞周期调控机制的操纵需要Rta和Zta的共同和相互作用。

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