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小泛素样修饰蛋白1(SUMO-1)对爱泼斯坦-巴尔病毒BZLF1功能及BMRF1表达的影响

Effects of SUMO-1 upon Epstein-Barr virus BZLF1 function and BMRF1 expression.

作者信息

Adamson Amy L

机构信息

Department of Biology, University of North Carolina at Greensboro, Greensboro, NC 27402, USA.

出版信息

Biochem Biophys Res Commun. 2005 Oct 14;336(1):22-8. doi: 10.1016/j.bbrc.2005.08.036.

Abstract

Epstein-Barr virus (EBV) is a human herpesvirus that has infected at least 90% of the world population. This very successful virus causes infectious mononucleosis and is associated with many different types of cancer. The EBV BZLF1 protein is a transcription factor that has also been shown to interact with many host cell proteins and pathways. BZLF1 (Z) is tagged by the small ubiquitin-related modifier-1 (SUMO-1) protein. Here, we present studies of the functional consequences of SUMO-1 modification of Z. We found that SUMO-1 modification of Z has no apparent effect upon the stability and localization of the Z protein. We did find, however, that SUMO-1 modification decreases the transactivation activity of Z on specific promoters. In addition, when SUMO-1 is supplied to cells when lytic replication is induced, EBV BMRF1 levels greatly increase, suggesting that SUMO-1 enhances EBV lytic replication. Therefore, SUMO-1 modification of proteins appears to have an important role in EBV lytic replication.

摘要

爱泼斯坦-巴尔病毒(EBV)是一种人类疱疹病毒,全球至少90%的人口都曾感染过。这种极为成功的病毒会引发传染性单核细胞增多症,并与多种不同类型的癌症相关。EBV的BZLF1蛋白是一种转录因子,也已被证明可与许多宿主细胞蛋白及信号通路相互作用。BZLF1(Z)被小泛素相关修饰物-1(SUMO-1)蛋白标记。在此,我们展示了对Z蛋白SUMO-1修饰的功能后果的研究。我们发现Z蛋白的SUMO-1修饰对Z蛋白的稳定性和定位没有明显影响。然而,我们确实发现SUMO-1修饰会降低Z蛋白对特定启动子的反式激活活性。此外,当在诱导裂解复制时向细胞提供SUMO-1时,EBV的BMRF1水平会大幅增加,这表明SUMO-1增强了EBV的裂解复制。因此,蛋白的SUMO-1修饰似乎在EBV裂解复制中起着重要作用。

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