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The Cauliflower Mosaic Virus Protein P6 Forms Motile Inclusions That Traffic along Actin Microfilaments and Stabilize Microtubules1,[W],[OA]

机译:花椰菜花叶病毒蛋白P6形成沿着肌动蛋白微丝运输并稳定微管的运动性内含物1,[W],[OA]

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The gene VI product (P6) of Cauliflower mosaic virus (CaMV) is a multifunctional protein known to be a major component of cytoplasmic inclusion bodies formed during CaMV infection. Although these inclusions are known to contain virions and are thought to be sites of translation from the CaMV 35S polycistronic RNA intermediate, the precise role of these bodies in the CaMV infection cycle remains unclear. Here, we examine the functionality and intracellular location of a fusion between P6 and GFP (P6-GFP). We initially show that the ability of P6-GFP to transactivate translation is comparable to unmodified P6. Consequently, our work has direct application for the large body of literature in which P6 has been expressed ectopically and its functions characterized. We subsequently found that P6-GFP forms highly motile cytoplasmic inclusion bodies and revealed through fluorescence colocalization studies that these P6-GFP bodies associate with the actin/endoplasmic reticulum network as well as microtubules. We demonstrate that while P6-GFP inclusions traffic along microfilaments, those associated with microtubules appear stationary. Additionally, inhibitor studies reveal that the intracellular movement of P6-GFP inclusions is sensitive to the actin inhibitor, latrunculin B, which also inhibits the formation of local lesions by CaMV in Nicotiana edwardsonii leaves. The motility of P6 along microfilaments represents an entirely new property for this protein, and these results imply a role for P6 in intracellular and cell-to-cell movement of CaMV.
机译:花椰菜花叶病毒(CaMV)的基因VI产物(P6)是一种多功能蛋白质,已知是CaMV感染期间形成的细胞质包涵体的主要成分。尽管这些内含物已知包含病毒体,并被认为是CaMV 35S多顺反子RNA中间体的翻译位点,但这些体在CaMV感染周期中的确切作用仍不清楚。在这里,我们检查了P6和GFP(P6-GFP)之间融合的功能和细胞内位置。我们最初显示P6-GFP反式激活翻译的能力与未修饰的P6相当。因此,我们的工作直接适用于其中异位表达P6及其功能表征的大量文献。我们随后发现P6-GFP形成了高度运动的细胞质包涵体,并通过荧光共定位研究揭示了这些P6-GFP体与肌动蛋白/内质网和微管相关。我们证明,虽然P6-GFP夹杂物沿着微丝运输,但那些与微管相关的东西似乎是静止的。此外,抑制剂研究表明P6-GFP内含物的细胞内运动对肌动蛋白抑制剂latrunculin B敏感,后者也抑制了CaMV在爱德华烟草叶片中局部损伤的形成。 P6沿微丝的运动性代表了该蛋白质的全新特性,这些结果暗示了P6在CaMV的细胞内和细胞间运动中的作用。

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