Department of Biochemistry and Cell Biology, State University of New York, Stony Brook, New York, USA.
Tobacco Breeding and Biotechnology Research Center, Yunnan Academy of Tobacco Agricultural Sciences, Kunming, Yunnan, China.
mBio. 2018 Jul 10;9(4):e01314-18. doi: 10.1128/mBio.01314-18.
Plant viruses cross the barrier of the plant cell wall by moving through intercellular channels, termed plasmodesmata, to invade their hosts. They accomplish this by encoding movement proteins (MPs), which act to alter plasmodesmal gating. How MPs target to plasmodesmata is not well understood. Our recent characterization of the first plasmodesmal localization signal (PLS) identified in a viral MP, namely, the MP encoded by the (TMV), now provides the opportunity to identify host proteins that recognize this PLS and may be important for its plasmodesmal targeting. One such candidate protein is synaptotagmin A (SYTA), which is required to form endoplasmic reticulum (ER)-plasma membrane contact sites and regulates the MP-mediated trafficking of begomoviruses, tobamoviruses, and potyviruses. In particular, SYTA interacts with, and regulates the cell-to-cell transport of, both TMV MP and the MP encoded by the (TVCV). Using bimolecular fluorescence complementation (BiFC) and yeast two-hybrid assays, we show here that the TMV PLS interacted with SYTA. This PLS sequence was both necessary and sufficient for interaction with SYTA, and the plasmodesmal targeting activity of the TMV PLS was substantially reduced in an knockdown line. Our findings show that SYTA is one host factor that can recognize the TMV PLS and suggest that this interaction may stabilize the association of TMV MP with plasmodesmata. Plant viruses use their movement proteins (MPs) to move through host intercellular connections, plasmodesmata. Perhaps one of the most intriguing, yet least studied, aspects of this transport is the MP signal sequences and their host recognition factors. Recently, we have described the plasmodesmal localization signal (PLS) of the (TMV) MP. Here, we identified the synaptotagmin A (SYTA) as a host factor that recognizes TMV MP PLS and promotes its association with the plasmodesmal membrane. The significance of these findings is two-fold: (i) we identified the TMV MP association with the cell membrane at plasmodesmata as an important PLS-dependent step in plasmodesmal targeting, and (ii) we identified the plant SYTA protein that specifically recognizes PLS as a host factor involved in this step.
植物病毒通过穿过细胞间通道(称为胞间连丝)来跨越植物细胞壁的障碍,从而侵入宿主。它们通过编码运动蛋白 (MP) 来实现这一点,这些蛋白可以改变胞间连丝的门控。MP 如何靶向胞间连丝尚不清楚。我们最近对病毒 MP 中鉴定的第一个胞间连丝定位信号 (PLS) 进行了表征,即编码烟草花叶病毒 (TMV) 的 MP,现在为鉴定识别该 PLS 的宿主蛋白并可能对其胞间连丝靶向很重要提供了机会。候选蛋白之一是突触结合蛋白 A (SYTA),它是形成内质网 (ER)-质膜接触位点所必需的,并且调节了贝科病毒、烟草花叶病毒和马铃薯 Y 病毒的 MP 介导的运输。特别是,SYTA 与 TMV MP 和编码 的 MP(TVCV)相互作用,并调节其细胞间运输。在这里,我们使用双分子荧光互补 (BiFC) 和酵母双杂交测定法表明,TMV PLS 与 SYTA 相互作用。该 PLS 序列对于与 SYTA 的相互作用是必要且充分的,并且在 knockdown 系中,TMV PLS 的质膜靶向活性大大降低。我们的发现表明 SYTA 是可以识别 TMV PLS 的一种宿主因子,并表明这种相互作用可能稳定 TMV MP 与胞间连丝的关联。植物病毒利用其运动蛋白 (MP) 通过宿主细胞间连接(胞间连丝)移动。在这种运输中,也许最有趣但研究最少的方面之一是 MP 信号序列及其宿主识别因子。最近,我们描述了 (TMV)MP 的胞间连丝定位信号 (PLS)。在这里,我们鉴定出 突触结合蛋白 A (SYTA) 作为一种宿主因子,它识别 TMV MP PLS 并促进其与质膜的关联。这些发现的意义有两方面:(i) 我们确定了 TMV MP 与质膜在胞间连丝处的关联是质膜靶向中一个重要的 PLS 依赖步骤,(ii) 我们鉴定出特异识别 PLS 的植物 SYTA 蛋白作为参与该步骤的宿主因子。