Yuan Cheng, Lazarowitz Sondra G, Citovsky Vitaly
Department of Biochemistry and Cell Biology, State University of New York;
Department of Plant Pathology and Plant-Microbe Biology, Cornell University.
J Vis Exp. 2017 Aug 15(126):55301. doi: 10.3791/55301.
Plasmodesmata (Pd) are cell-to-cell connections that function as gateways through which small and large molecules are transported between plant cells. Whereas Pd transport of small molecules, such as ions and water, is presumed to occur passively, cell-to-cell transport of biological macromolecules, such proteins, most likely occurs via an active mechanism that involves specific targeting signals on the transported molecule. The scarcity of identified plasmodesmata (Pd) localization signals (PLSs) has severely restricted the understanding of protein-sorting pathways involved in plant cell-to-cell macromolecular transport and communication. From a wealth of plant endogenous and viral proteins known to traffic through Pd, only three PLSs have been reported to date, all of them from endogenous plant proteins. Thus, it is important to develop a reliable and systematic experimental strategy to identify a functional PLS sequence, that is both necessary and sufficient for Pd targeting, directly in the living plant cells. Here, we describe one such strategy using as a paradigm the cell-to-cell movement protein (MP) of the Tobacco mosaic virus (TMV). These experiments, that identified and characterized the first plant viral PLS, can be adapted for discovery of PLS sequences in most Pd-targeted proteins.
胞间连丝(Pd)是细胞间的连接通道,充当小分子和大分子在植物细胞间运输的门户。虽然离子和水等小分子通过胞间连丝的运输被认为是被动发生的,但生物大分子(如蛋白质)在细胞间的运输很可能是通过一种主动机制进行的,这种机制涉及被运输分子上的特定靶向信号。已鉴定的胞间连丝(Pd)定位信号(PLS)非常稀少,这严重限制了我们对植物细胞间大分子运输和通讯中蛋白质分选途径的理解。在众多已知通过胞间连丝运输的植物内源蛋白和病毒蛋白中,迄今为止仅报道了三种PLS,且均来自植物内源蛋白。因此,开发一种可靠且系统的实验策略,以直接在活植物细胞中鉴定出对Pd靶向既必要又充分的功能性PLS序列非常重要。在此,我们描述了一种以烟草花叶病毒(TMV)的细胞间运动蛋白(MP)为范例的策略。这些鉴定并表征了首个植物病毒PLS的实验,可用于发现大多数靶向Pd的蛋白质中的PLS序列。