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Ammonia-regulated expression of a soybean gene encoding cytosolic glutamine synthetase in transgenic Lotus corniculatus.

机译:氨调节转基因莲花角ic中编码胞质谷氨酰胺合成酶的大豆基因的表达。

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摘要

A full-length cDNA clone encoding cytosolic glutamine synthetase (GS), expressed in roots and root nodules of soybean, was isolated by direct complementation of an Escherichia coli gln A- mutant. This sequence is induced in roots by the availability of ammonia. A 3.5-kilobase promoter fragment of a genomic clone (lambda GS15) corresponding to this cDNA was isolated and fused with a reporter [beta-glucuronidase (GUS)] gene. The GS-GUS fusion was introduced into a legume (Lotus corniculatus) and a nonlegume (tobacco) plant by way of Agrobacterium-mediated transformations. This chimeric gene was found to be expressed in a root-specific manner in both tobacco and L. corniculatus, the expression being restricted to the growing root apices and the vascular bundles of the mature root. Treatment with ammonia increased the expression of this chimeric gene in the legume background (i.e., L. corniculatus); however, no induction was observed in tobacco roots. Histochemical localization of GUS activity in ammonia-treated transgenic L. corniculatus roots showed a uniform distribution across all cell types. These data suggest that the tissue specificity of the soybean cytosolic GS gene is conserved in both tobacco and L. corniculatus; however, in the latter case, this gene is ammonia inducible. Furthermore, the ammonia-enhanced GS gene expression in L. corniculatus is due to an increase in transcription. That this gene is directly regulated by externally supplied or symbiotically fixed nitrogen is also evident from the expression of GS-GUS in the infection zone, including the uninfected cells, and the inner cortex of transgenic L. corniculatus nodules, where a flux of ammonia is encountered by this tissue. The lack of expression of GS-GUS in the outer cortex of the nodules suggests that ammonia may not be able to diffuse outside the endodermis.
机译:通过直接互补大肠杆菌gln A-突变体分离了在大豆根和根瘤中表达的编码胞质谷氨酰胺合成酶(GS)的全长cDNA克隆。氨的可利用性在根中诱导了该序列。分离对应于该cDNA的基因组克隆(λGS15)的3.5-千碱基启动子片段,并与报道基因[β-葡糖醛酸糖苷酶(GUS)]基因融合。 GS-GUS融合物通过农杆菌介导的转化被引入到豆类(Cortus corniculatus)和非豆类(烟草)植物中。发现该嵌合基因以根特异性的方式在烟草和L.corniculatus中表达,该表达限于生长中的根尖和成熟根的维管束。用氨处理增加了该嵌合基因在豆类背景(即,L.corniculatus)中的表达。然而,在烟草根中未观察到诱导作用。 GUS活性在氨水处理的转基因山茱。根中的组织化学定位显示在所有细胞类型中均一分布。这些数据表明大豆胞质GS基因的组织特异性在烟草和L.corniculatus中均是保守的。然而,在后一种情况下,该基因是氨可诱导的。此外,由于L.corniculatus中氨增强的GS基因表达,是由于转录增加所致。 GS-GUS在感染区(包括未感染的细胞)和转基因L. corniculatus结节的内部皮层中的表达,也可以通过外部供应的或共生固定的氮直接调节该基因,其中氨通量是遇到这种组织。结节外皮层中缺乏GS-GUS表达,这表明氨可能无法扩散到真皮内。

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