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Differing requirements for actin and myosin by plant viruses for sustained intercellular movement

机译:植物病毒对肌动蛋白和肌球蛋白的持续细胞间移动的不同要求

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The actin cytoskeleton has been implicated in the intra- and intercellular movement of a growing number of plant and animal viruses. However, the range of viruses influenced by actin for movement and the mechanism of this transport are poorly understood. Here we determine the importance of microfilaments and myosins for the sustained intercellular movement of a group of RNA-based plant viruses. We demonstrate that the intercellular movement of viruses from different genera [tobacco mosaic virus (TMV), potato virus X (PVX), tomato bushy stunt virus (TBSV)], is inhibited by disruption of microfilaments. Surprisingly, turnip vein-clearing virus (TVCV), a virus from the same genus as TMV, did not require intact microfilaments for normal spread. To investigate the molecular basis for this difference we compared the subcellular location of GFP fusions to the 126-kDa protein and the homologous 125-kDa protein from TMV and TVCV, respectively. The 126-kDa protein formed numerous large cytoplasmic inclusions associated with microfilaments, whereas the 125-kDa protein formed few small possible inclusions, none associated with microfilaments. The dependence of TMV, PVX, and TBSV on intact microfilaments for intercellular movement led us to investigate the role of myosin motors in this process. Virus-induced gene silencing of the Nico-tiana benthamiana myosin XI-2 gene, but not three other myosins, inhibited only TMV movement. These results indicate that RNA viruses have evolved differently in their requirements for microfilaments and the associated myosin motors, in a manner not correlated with predicted phylogeny.
机译:肌动蛋白的细胞骨架与越来越多的植物和动物病毒的细胞内和细胞间运动有关。但是,人们对肌动蛋白影响运动的病毒范围和这种运输的机理了解得很少。在这里,我们确定了微丝和肌球蛋白对于一组基于RNA的植物病毒的持续细胞间运动的重要性。我们证明了来自不同属的病毒[烟草花叶病毒(TMV),马铃薯病毒X(PVX),番茄浓密特技病毒(TBSV)]的细胞间运动受到微丝破坏的抑制。令人惊讶的是,芜菁静脉清除病毒(TVCV)是与TMV属相同的病毒,不需要完整的微丝即可正常传播。为了研究这种差异的分子基础,我们比较了GFP融合蛋白的亚细胞位置与分别来自TMV和TVCV的126 kDa蛋白和同源125 kDa蛋白。 126 kDa蛋白质形成许多与微丝相关的大胞质内含物,而125 kDa蛋白形成少量可能的小夹杂物,与微丝无关。 TMV,PVX和TBSV对完整微丝在细胞间运动中的依赖性使我们研究了肌球蛋白运动在此过程中的作用。烟草诱导的本氏烟草尼古丁肌球蛋白XI-2基因的病毒诱导的基因沉默,但不抑制其他三种肌球蛋白,仅抑制TMV运动。这些结果表明,RNA病毒对微丝和相关肌球蛋白运动的要求已经以与预测的系统发育无关的方式进化。

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