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苜蓿银纹夜蛾多核多角体病毒是核衣壳核出芽和核内微泡形成所必需的。

Autographa californica Multiple Nucleopolyhedrovirus Is Required for the Nuclear Egress of Nucleocapsids and Intranuclear Microvesicle Formation.

作者信息

Shi Anqi, Hu Zhaoyang, Zuo Yachao, Wang Yan, Wu Wenbi, Yuan Meijin, Yang Kai

机构信息

State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China.

State Key Laboratory of Biocontrol, Sun Yat-sen University, Guangzhou, China

出版信息

J Virol. 2018 Jan 30;92(4). doi: 10.1128/JVI.01509-17. Print 2018 Feb 15.

Abstract

Autographa californica multiple nucleopolyhedrovirus (AcMNPV) () is a highly conserved gene of unknown function. In this study, we constructed an knockout AcMNPV bacmid and investigated the role of in the baculovirus life cycle. The expression and distribution of the Ac75 protein were characterized, and its interaction with another viral protein was analyzed to further understand its function. Our data indicated that was required for the nuclear egress of nucleocapsids, intranuclear microvesicle formation, and subsequent budded virion (BV) formation, as well as occlusion-derived virion (ODV) envelopment and embedding of ODVs into polyhedra. Western blot analyses showed that two forms, of 18 and 15 kDa, of FLAG-tagged Ac75 protein were detected. Ac75 was associated with both nucleocapsid and envelope fractions of BVs but with only the nucleocapsid fraction of ODVs; the 18-kDa form was associated with only BVs, whereas the 15-kDa form was associated with both types of virion. Ac75 was localized predominantly in the intranuclear ring zone during infection and exhibited a nuclear rim distribution during the early phase of infection. A phase separation assay suggested that Ac75 was not an integral membrane protein. A coimmunoprecipitation assay revealed an interaction between Ac75 and the integral membrane protein Ac76, and bimolecular fluorescence complementation assays identified the sites of the interaction within the cytoplasm and at the nuclear membrane and ring zone in AcMNPV-infected cells. Our results have identified as a second gene that is required for both the nuclear egress of nucleocapsids and the formation of intranuclear microvesicles. During the baculovirus life cycle, the morphogenesis of both budded virions (BVs) and occlusion-derived virions (ODVs) is proposed to involve a budding process at the nuclear membrane, which occurs while nucleocapsids egress from the nucleus or when intranuclear microvesicles are produced. However, the exact mechanism of virion morphogenesis remains unknown. In this study, we identified as a second gene, in addition to , that is essential for the nuclear egress of nucleocapsids, intranuclear microvesicle formation, and subsequent BV formation, as well as ODV envelopment and embedding of ODVs into polyhedra. Ac75 is not an integral membrane protein. However, it interacts with an integral membrane protein (Ac76) and is associated with the nuclear membrane. These data enhance our understanding of the commonalities between nuclear egress of nucleocapsids and intranuclear microvesicle formation and may help to reveal insights into the mechanism of baculovirus virion morphogenesis.

摘要

苜蓿银纹夜蛾多核多角体病毒(AcMNPV)的Ac75是一个功能未知的高度保守基因。在本研究中,我们构建了Ac75基因敲除的AcMNPV杆粒,并研究了Ac75在杆状病毒生命周期中的作用。对Ac75蛋白的表达和分布进行了表征,并分析了其与另一种病毒蛋白的相互作用,以进一步了解其功能。我们的数据表明,Ac75是核衣壳核出芽、核内微泡形成以及随后的出芽病毒粒子(BV)形成所必需的,也是包涵体衍生病毒粒子(ODV)包膜化以及ODV嵌入多角体所必需的。蛋白质免疫印迹分析表明,检测到两种形式的带有FLAG标签的Ac75蛋白,分子量分别为18 kDa和15 kDa。Ac75与BV的核衣壳和包膜部分都有关联,但仅与ODV的核衣壳部分有关联;18 kDa的形式仅与BV有关联,而15 kDa的形式与两种类型的病毒粒子都有关联。在感染期间,Ac75主要定位于核内环区,在感染早期呈现核边缘分布。相分离分析表明Ac75不是整合膜蛋白。免疫共沉淀分析揭示了Ac75与整合膜蛋白Ac76之间存在相互作用,双分子荧光互补分析确定了在AcMNPV感染细胞的细胞质内、核膜和环区的相互作用位点。我们的结果确定Ac75是核衣壳核出芽和核内微泡形成所需的第二个基因。在杆状病毒生命周期中,出芽病毒粒子(BV)和包涵体衍生病毒粒子(ODV)的形态发生都被认为涉及在核膜处的出芽过程,这一过程发生在核衣壳从细胞核中出芽时或产生核内微泡时。然而,病毒粒子形态发生的确切机制仍然未知。在本研究中,我们确定Ac75是除Ac74外的第二个基因,它对于核衣壳核出芽、核内微泡形成以及随后的BV形成,以及ODV包膜化和ODV嵌入多角体都是必不可少的。Ac75不是整合膜蛋白。然而,它与一种整合膜蛋白(Ac76)相互作用并与核膜相关联。这些数据加深了我们对核衣壳核出芽和核内微泡形成之间共性的理解,并可能有助于揭示杆状病毒粒子形态发生机制的见解。

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