Taoka Ken-Ichiro, Ham Byung-Kook, Xoconostle-Cázares Beatriz, Rojas Maria R, Lucas William J
Section of Plant Biology, College of Biological Sciences, University of California, Davis, CA 95616, USA.
Plant Cell. 2007 Jun;19(6):1866-84. doi: 10.1105/tpc.107.052522. Epub 2007 Jun 29.
In plants, cell-to-cell trafficking of non-cell-autonomous proteins (NCAPs) involves protein-protein interactions, and a role for posttranslational modification has been implicated. In this study, proteins contained in pumpkin (Cucurbita maxima cv Big Max) phloem sap were used as a source of NCAPs to further explore the molecular basis for selective NCAP trafficking. Protein overlay assays and coimmunoprecipitation experiments established that phosphorylation and glycosylation, on both Nicotiana tabacum NON-CELL-AUTONOMOUS PATHWAY PROTEIN1 (Nt-NCAPP1) and the phloem NCAPs, are essential for their interaction. Detailed molecular analysis of a representative phloem NCAP, Cm-PP16-1, identified the specific residues on which glycosylation and phosphorylation must occur for effective binding to NCAPP1. Microinjection studies confirmed that posttranslational modification on these residues is essential for cell-to-cell movement of Cm-PP16-1. Lastly, a glutathione S-transferase (GST)-Cm-PP16-1 fusion protein system was employed to test whether the peptide region spanning these residues was required for cell-to-cell movement. These studies established that a 36-amino acid peptide was sufficient to impart cell-to-cell movement capacity to GST, a normally cell-autonomous protein. These findings are consistent with the hypothesis that a phosphorylation-glycosylation recognition motif functions to control the binding of a specific subset of phloem NCAPs to NCAPP1 and their subsequent transport through plasmodesmata.
在植物中,非细胞自主性蛋白(NCAPs)的细胞间运输涉及蛋白质-蛋白质相互作用,并且翻译后修饰也被认为发挥了作用。在本研究中,南瓜(西葫芦品种大马克斯)韧皮部汁液中所含的蛋白质被用作NCAPs的来源,以进一步探索选择性NCAP运输的分子基础。蛋白质印迹分析和免疫共沉淀实验表明,烟草非细胞自主性通路蛋白1(Nt-NCAPP1)和韧皮部NCAPs上的磷酸化和糖基化对于它们之间的相互作用至关重要。对一种代表性的韧皮部NCAP——Cm-PP16-1进行详细的分子分析,确定了糖基化和磷酸化必须发生在其上才能有效结合NCAPP1的特定残基。显微注射研究证实,这些残基上的翻译后修饰对于Cm-PP16-1的细胞间移动至关重要。最后,采用谷胱甘肽S-转移酶(GST)-Cm-PP16-1融合蛋白系统来测试跨越这些残基的肽区域对于细胞间移动是否必需。这些研究表明一个36个氨基酸的肽足以赋予GST(一种通常为细胞自主性的蛋白)细胞间移动能力。这些发现与以下假设一致:磷酸化-糖基化识别基序发挥作用,控制韧皮部NCAPs的特定子集与NCAPP1的结合及其随后通过胞间连丝的运输。