首页> 美国卫生研究院文献>Journal of Virology >Note: Leptomycin B Inhibits Equine Infectious Anemia Virus Rev and Feline Immunodeficiency Virus Rev Function but Not the Function of the Hepatitis B Virus Posttranscriptional Regulatory Element
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Note: Leptomycin B Inhibits Equine Infectious Anemia Virus Rev and Feline Immunodeficiency Virus Rev Function but Not the Function of the Hepatitis B Virus Posttranscriptional Regulatory Element

机译:注意:Leptomycin B抑制马传染性贫血病毒Rev和猫免疫缺陷病毒Rev功能但不抑制乙肝病毒转录后调控元件的功能

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摘要

Human immunodeficiency virus type 1 Rev export depends upon the presence of the nuclear export signal (NES), a leucine-rich stretch of hydrophobic amino acids. Recently, the nuclear NES-binding receptor has been identified as CRM1 or exportin 1. Rev export has been shown to be CRM1 dependent. The function of the atypical NES-containing Rev-like proteins of equine infectious anemia virus (EIAV) and feline immunodeficiency virus (FIV) is inhibited by leptomycin B, a drug that specifically blocks NES-CRM1 interactions. These data suggest that the function of atypical NES-containing proteins is CRM1 dependent. In contrast to the inhibition of EIAV Rev and FIV Rev, the cytoplasmic accumulation of hepatitis B virus (HBV) posttranscriptional regulatory element (PRE)-containing and Mason-Pfizer monkey virus (MPMV) constitutive transport element (CTE)-containing RNAs is not inhibited by leptomycin B treatment. We conclude that the HBV PRE, like the MPMV CTE, functions independently of an NES receptor-exportin 1 interaction.
机译:1型人类免疫缺陷病毒的Rev出口取决于核出口信号(NES)的存在,核出口信号是富含亮氨酸的疏水氨基酸。最近,核NES结合受体被鉴定为CRM1或输出蛋白1。Rev输出已显示是CRM1依赖性的。马传染性贫血病毒(EIAV)和猫免疫缺陷病毒(FIV)的非典型的含NES Rev样蛋白的功能受瘦素B的抑制,瘦素B是一种特异性阻断NES-CRM1相互作用的药物。这些数据表明非典型NES蛋白质的功能是CRM1依赖的。与EIAV Rev和FIV Rev的抑制相反,乙肝病毒(HBV)转录后调控元件(PRE)和梅森-辉瑞猴病毒(MPMV)组成性转运元件(CTE)的RNA的胞质积累不被瘦霉素B抑制。我们得出的结论是,像MPMV CTE一样,HBV PRE的功能独立于NES受体-exportin 1相互作用。

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