首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >The neural F-box protein NFB42 mediates the nuclear export of the herpes simplex virus type 1 replication initiator protein (UL9 protein) after viral infection
【24h】

The neural F-box protein NFB42 mediates the nuclear export of the herpes simplex virus type 1 replication initiator protein (UL9 protein) after viral infection

机译:神经F盒蛋白NFB42介导病毒感染后1型单纯疱疹病毒复制起始蛋白(UL9蛋白)的核输出。

获取原文
获取原文并翻译 | 示例
       

摘要

The neural F-box 42-kDa protein (NFB42) is a component of the SCFNFB42 E3 ubiquitin ligase that is expressed in all major areas of the brain; it is not detected in nonneuronal tissues. We previously identified NFB42 as a binding partner for the herpes simplex virus 1 (HSV-1) UL9 protein, the viral replication-initiator, and showed that coexpression of NFB42 and UL9 in human embryonic kidney (293T) cells led to a significant decrease in the level of UL9 protein. We have now found that HSV-1 infection promotes the shuttling of NFB42 between the cytosol and the nucleus in both 293T cells and primary hippocampal neurons, permitting NFB42 to bind to the phosphorylated UL9 protein, which is localized in the nucleus. This interaction mediates the export of the UL9 protein from the nucleus to the cytosol, leading to its ubiquitination and degradation via the 26S proteasome. Because the intranuclear localization of the UL9 protein, along with other viral and cellular factors, is an essential step in viral DNA replication, degradation of the UL9 protein in neurons by means of nuclear export through its specific interaction with NFB42 may prevent active replication and promote neuronal latency of HSV-1. [References: 42]
机译:神经F-box 42-kDa蛋白(NFB42)是SCFNFB42 E3泛素连接酶的一个组成部分,在大脑的所有主要区域都有表达。在非神经组织中未检测到。我们先前将NFB42确定为单纯疱疹病毒1(HSV-1)UL9蛋白(病毒复制引发剂)的结合伴侣,并表明NFB42和UL9在人胚肾(293T)细胞中的共表达可导致NFB42和UL9的显着减少。 UL9蛋白的水平。现在我们已经发现,HSV-1感染促进了293T细胞和原代海马神经元在细胞质和细胞核之间NFB42的穿梭,使NFB42与位于细胞核中的磷酸化UL9蛋白结合。这种相互作用介导了UL9蛋白从细胞核到细胞质的输出,导致其泛素化并通过26S蛋白酶体降解。由于UL9蛋白的核内定位以及其他病毒和细胞因子是病毒DNA复制中的必不可少的步骤,因此通过与NFB42的特异性相互作用通过核输出而使神经元中的UL9蛋白降解可能会阻止活性复制并促进HSV-1的神经元潜伏期。 [参考:42]

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号