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花椰菜花叶病毒的蚜虫传播因子在昆虫和植物细胞中均与微管形成稳定的复合体。

The aphid transmission factor of cauliflower mosaic virus forms a stable complex with microtubules in both insect and plant cells.

作者信息

Blanc S, Schmidt I, Vantard M, Scholthof H B, Kuhl G, Esperandieu P, Cerutti M, Louis C

机构信息

Station de Recherches de Pathologie Comparée, Institut National de la Recherche Agronomique, Centre National de la Recherche Scientifique, Christol-les-Alès, France.

出版信息

Proc Natl Acad Sci U S A. 1996 Dec 24;93(26):15158-63. doi: 10.1073/pnas.93.26.15158.

Abstract

We analyzed the distribution of the cauliflower mosaic virus (CaMV) aphid transmission factor (ATF), produced via a baculovirus recombinant, within Sf9 insect cells. Immunogold labeling revealed that the ATF colocalizes with an atypical cytoskeletal network. Detailed observation by electron microscopy demonstrated that this network was composed of microtubules decorated with paracrystalline formations, characteristic of the CaMV ATF. A derivative mutant of the ATF, unable to self-assemble into paracrystals, was also analyzed. This mutant formed a net-like structure, with a mesh of four nanometers, tightly sheathing microtubules. Both the ATF- and the derivative mutant-microtubule complexes were highly stable. They resisted dilution-, cold-, and calcium-induced microtubule disassembly as well as a combination of all three for over 6 hr. CaMV ATF cosedimented with microtubules and, surprisingly, it bound to Taxol-stabilized microtubules at high ionic strength, thus suggesting an atypical interaction when compared with that usually described for microtubule-binding proteins. Using immunofluorescence double labeling we also demonstrated that the CaMV ATF colocalizes with the microtubule network when expressed in plant cells.

摘要

我们分析了通过杆状病毒重组体产生的花椰菜花叶病毒(CaMV)蚜虫传播因子(ATF)在Sf9昆虫细胞内的分布。免疫金标记显示ATF与一个非典型细胞骨架网络共定位。电子显微镜的详细观察表明,该网络由装饰有副晶体结构的微管组成,这是CaMV ATF的特征。我们还分析了一种无法自组装成副晶体的ATF衍生突变体。该突变体形成了一个网状结构,其网眼为4纳米,紧密包裹着微管。ATF和衍生突变体 - 微管复合物都非常稳定。它们在超过6小时的时间里抵抗了稀释、低温和钙诱导的微管解聚,以及这三种因素的组合诱导的微管解聚。CaMV ATF与微管共同沉降,令人惊讶的是,它在高离子强度下与紫杉醇稳定的微管结合,因此与通常描述的微管结合蛋白相比,这表明存在一种非典型相互作用。使用免疫荧光双重标记,我们还证明了CaMV ATF在植物细胞中表达时与微管网络共定位。

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