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Nodule-specific modulation of glutamine synthetase in transgenic Medicago truncatula leads to inverse alterations in asparagine synthetase expression

机译:转基因紫花苜蓿中谷氨酰胺合成酶的结节特异性调节导致天冬酰胺合成酶表达的反向改变

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Transgenic Medicago truncatula plants were produced harboring chimeric gene constructs of the glutamine synthetase (GS) cDNA clones (MtGS1a or MtGS1b) fused in sense or antisense orientation to the nodule-specific leghemoglobin promoter Mtlb1. A series of transgenic plants were obtained showing a 2- to 4-fold alteration in nodule GS activity when compared with control plants. Western and northern analyses revealed that the increased or decreased levels of GS activity correlate with the amount of cytosolic GS polypeptides and transcripts present in the nodule extracts. An analysis of the isoenzyme composition showed that the increased or decreased levels of GS activity were attributable to major changes in the homo-octameric isoenzyme GS1a. Nodules of plants transformed with antisense GS constructs showed an increase in the levels of both asparagine synthetase (AS) polypeptides and transcripts when compared with untransformed control plants, whereas the sense GS transformants showed decreased AS transcript levels but polypeptide levels similar to control plants. The polypeptide abundance of other nitrogen metabolic enzymes NADH-glutamic acid synthase and aspartic acid aminotransferase as well as those of major carbon metabolic enzymes phosphoenolpyruvate carboxylase, carbonic anhydrase, and sucrose synthase were not affected by the GS-gene manipulations. Increased levels of AS polypeptides and transcripts were also transiently observed in nodules by inhibiting GS activity with phosphinothricin. Taken together, the results presented here suggest that GS activity negatively regulates the level of AS in root nodules of M. truncatula. The potential role of AS in assimilating ammonium when GS becomes limiting is discussed. [References: 51]
机译:产生了带有谷氨酰胺合成酶(GS)cDNA克隆(MtGS1a或MtGS1b)的嵌合基因构建体的转基因紫花苜蓿植物,该基因克隆以有义或反义方向与结节特异性豆血红蛋白启动子Mtlb1融合。与对照植物相比,获得了一系列转基因植物,其结节GS活性显示出2-4倍的变化。西方和北方的分析表明,GS活性的升高或降低与根瘤提取物中存在的胞质GS多肽和转录物的数量有关。对同工酶组成的分析表明,GS活性水平的升高或降低归因于同八聚体同工酶GS1a的重大变化。与未转化的对照植物相比,用反义GS构建体转化的植物的结节显示天冬酰胺合成酶(AS)多肽和转录物的水平均增加,而有义GS转化体显示出AS转录物水平降低但多肽水平与对照植物相似。 GS基因操作不影响其他氮代谢酶NADH-谷氨酸合酶和天冬氨酸转氨酶以及主要碳代谢酶磷酸烯醇丙酮酸羧化酶,碳酸酐酶和蔗糖合酶的多肽丰度。通过用膦丝菌素抑制GS活性,在结节中也瞬时观察到AS多肽和转录物水平的增加。两者合计,这里呈现的结果表明GS活性负调节M.truncatula根瘤中AS的水平。讨论了当GS变得有限时,AS在吸收铵中的潜在作用。 [参考:51]

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