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鉴定 PRV UL54 核质穿梭的分子决定因素。

Characterization of molecular determinants for nucleocytoplasmic shuttling of PRV UL54.

机构信息

State Key Laboratory of Virology, Wuhan Institute of Virology, Chinese Academy of Sciences, Wuhan 430071, China.

出版信息

Virology. 2011 Sep 1;417(2):385-93. doi: 10.1016/j.virol.2011.06.004. Epub 2011 Jul 20.

Abstract

The pseudorabies virus (PRV) early protein UL54 is a homologue of the herpes simplex virus 1 (HSV-1) immediate-early protein ICP27, which is a multifunctional protein and essential for HSV-1 infection. To determine if UL54 might shuttle between the nucleus and cytoplasm, as has been shown for its homologues in human herpesviruses, the molecular determinants for its nucleocytoplasmic shuttling were investigated. Heterokaryon assays demonstrated that UL54 was a nucleocytoplasmic shuttling protein and this property could not be blocked by leptomycin B, an inhibitor of chromosome region maintenance 1 (CRM1). However, TAP/NXF1 promoted the nuclear export of UL54 and interacted with UL54, suggesting that UL54 shuttles between the nucleus and the cytoplasm via a TAP/NXF1, but not CRM1, dependent nuclear export pathway. Furthermore, UL54 was demonstrated to target to the nucleus through a classic Ran-, importin β1- and α5-dependent nuclear import mechanism.

摘要

伪狂犬病毒 (PRV) 早期蛋白 UL54 是单纯疱疹病毒 1 (HSV-1) 即刻早期蛋白 ICP27 的同源物,后者是一种多功能蛋白,对 HSV-1 感染至关重要。为了确定 UL54 是否像其在人类疱疹病毒中的同源物那样在核和细胞质之间穿梭,研究了其核质穿梭的分子决定因素。杂种核试验表明 UL54 是一种核质穿梭蛋白,该性质不能被莱普霉素 B(CRM1 的抑制剂)阻断。然而,TAP/NXF1 促进 UL54 的核输出并与 UL54 相互作用,表明 UL54 通过 TAP/NXF1,而不是 CRM1,依赖的核输出途径在核和细胞质之间穿梭。此外,已证明 UL54 通过经典的 Ran、importin β1 和 α5 依赖的核输入机制靶向细胞核。

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