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首页> 外文期刊>The Plant Cell >Lost in Transit: Long-Distance Trafficking and Phloem Unloading of Protein Signals in Arabidopsis Homografts
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Lost in Transit: Long-Distance Trafficking and Phloem Unloading of Protein Signals in Arabidopsis Homografts

机译:途中丢失:拟南芥同种异体中蛋白质信号的远距离贩运和韧皮部卸载

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In addition to moving sugars and nutrients, the phloem transports many macromolecules. While grafting and aphid stylectomy experiments have identified many macromolecules that move in the phloem, the functional significance of phloem transport of these remains unclear. To gain insight into protein trafficking, we micrografted Arabidopsis thaliana scions expressing GFP-tagged chloroplast transit peptides under the 35S promoter onto nontransgenic rootstocks. We found that plastids in the root tip became fluorescent 10 d after grafting. We obtained identical results with the companion cell-specific promoter SUC2 and with signals that target proteins to peroxisomes, actin, and the nucleus. We were unable to detect the respective mRNAs in the rootstock, indicating extensive movement of proteins in the phloem. Outward movement from the root protophloem was restricted to the pericycle-endodermis boundary, identifying plasmodesmata at this interface as control points in the exchange of macromolecules between stele and cortex. Intriguingly, signals directing proteins to the endoplasmic reticulum and Golgi apparatus from membrane-bound ribosomes were not translocated to the root. It appears that many organelle-targeting sequences are insufficient to prevent the loss of their proteins into the translocation stream. Thus, nonspecific loss of proteins from companion cells to sieve elements may explain the plethora of macromolecules identified in phloem sap.
机译:韧皮部除了移动糖和营养素外,还运输许多大分子。虽然嫁接和蚜虫切开术实验已经确定了许多在韧皮部中移动的大分子,但这些韧皮部转运的功能意义仍不清楚。为了深入了解蛋白质运输,我们将拟南芥接穗在35S启动子下微生表达GFP标记的叶绿体转运肽,移植到非转基因砧木上。我们发现嫁接后10 d,根尖中的质体变为荧光。我们获得了与伴侣细胞特异性启动子SUC2和信号针对过氧化物酶体,肌动蛋白和细胞核的信号相同的结果。我们无法检测到砧木中的各个mRNA,表明韧皮部中蛋白质的广泛运动。从根原上皮的向外运动被限制在周周-内皮层边界,从而在该界面处将胞质寄生虫识别为石碑和皮层之间大分子交换的控制点。有趣的是,将信号从膜结合核糖体引导至内质网和高尔基体的信号并未转移到根部。似乎许多靶向细胞器的序列不足以防止其蛋白质损失到易位流中。因此,蛋白质从伴侣细胞到筛分元件的非特异性损失可能解释了韧皮部汁液中鉴定出的大量大分子。

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