首页> 外文期刊>Frontiers in Plant Science >Suppressor mutations in the Glutamine Dumper1 protein dissociate disturbance in amino acid transport from other characteristics of the Gdu1D phenotype
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Suppressor mutations in the Glutamine Dumper1 protein dissociate disturbance in amino acid transport from other characteristics of the Gdu1D phenotype

机译:谷氨酰胺Dumper1蛋白中的抑制子突变与Gdu1D表型的其他特征解除了氨基酸转运的干扰

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Intracellular amino acid transport across plant membranes is critical for metabolic pathways which are often split between different organelles. In addition, transport of amino acids across the plasma membrane enables the distribution of organic nitrogen through the saps between leaves and developing organs. Amino acid importers have been studied for more than two decades, and their role in this process is well-documented. While equally important, amino acid exporters are not well-characterized. The over-expression of GDU1 , encoding a small membrane protein with one transmembrane domain, leads to enhancement of amino acid export by Arabidopsis cells, glutamine secretion at the leaf margin, early senescence and size reduction of the plant, possibly caused by the stimulation of amino acid exporter(s). Previous work reported the identification of suppressor mutations of the GDU1 over-expression phenotype, which affected the GDU1 and LOG2 genes, the latter encoding a membrane-bound ubiquitin ligase interacting with GDU1. The present study focuses on the characterization of three additional suppressor mutations affecting GDU1 . Size, phenotype, glutamine transport and amino acid tolerance were recorded for recapitulation plants and over-expressors of mutagenized GDU1 proteins. Unexpectedly, the over-expression of most mutated GDU1 led to plants with enhanced amino acid export, but failing to display secretion of glutamine and size reduction. The results show that the various effects triggered by GDU1 over-expression can be dissociated from one another by mutagenizing specific residues. The fact that these residues are not necessarily conserved suggests that the diverse biochemical properties of the GDU1 protein are not only born by the characterized transmembrane and VIMAG domains. These data provide a better understanding of the structure/function relationships of GDU1 and may enable modifying amino acid export in plants without detrimental effects on plant fitness.
机译:跨植物膜的细胞内氨基酸运输对于通常在不同细胞器之间分裂的代谢途径至关重要。另外,氨基酸跨质膜的转运使有机氮通过叶片和发育器官之间的汁液分布。氨基酸进口商已被研究了二十多年,其在这一过程中的作用已得到充分证明。尽管同等重要,但氨基酸出口商的特征并不充分。编码具有一个跨膜结构域的小膜蛋白的GDU1的过表达导致拟南芥细胞的氨基酸输出增加,叶边缘的谷氨酰胺分泌,植物的早期衰老和尺寸减小,这可能是由于刺激了氨基酸出口商。先前的工作报道了GDU1过表达表型的抑制突变的鉴定,该突变影响了GDU1和LOG2基因,后者编码与GDU1相互作用的膜结合型泛素连接酶。本研究的重点是表征影响GDU1的三个其他抑制突变。记录了重配植物和诱变的GDU1蛋白的过表达子的大小,表型,谷氨酰胺转运和氨基酸耐受性。出乎意料的是,大多数突变的GDU1的过表达导致植物具有增强的氨基酸输出,但未能显示出谷氨酰胺的分泌和尺寸减小。结果表明,通过诱变特定残基可以使由GDU1过表达触发的各种作用相互分离。这些残基不一定是保守的事实表明,GDU1蛋白的多种生化特性不仅由特征化的跨膜和VIMAG结构域决定。这些数据提供了对GDU1的结构/功能关系的更好理解,并且可以使植物中的氨基酸输出得到修饰,而对植物适应性没有不利影响。

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