首页> 外文期刊>Plant Molecular Biology >IDENTIFICATION OF SEVERAL SOYBEAN CYTOSOLIC GLUTAMINE SYNTHETASE TRANSCRIPTS HIGHLY OR SPECIFICALLY EXPRESSED IN NODULES - EXPRESSION STUDIES USING ONE OF THE CORRESPONDING GENES IN TRANSGENIC LOTUS CORNICULATUS
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IDENTIFICATION OF SEVERAL SOYBEAN CYTOSOLIC GLUTAMINE SYNTHETASE TRANSCRIPTS HIGHLY OR SPECIFICALLY EXPRESSED IN NODULES - EXPRESSION STUDIES USING ONE OF THE CORRESPONDING GENES IN TRANSGENIC LOTUS CORNICULATUS

机译:在结节中高表达或特定表达的几种大豆胞液谷氨酰胺合成酶转录的鉴定-使用转基因荷花莲中一种对应的基因进行表达研究

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摘要

A DNA fragment containing sequences hybridizing to the 5' region of GS15, a gene encoding soybean cytosolic glutamine synthetase, was isolated from a soybean genomic library. Mapping and partial sequence analysis of the genomic clone revealed that it encodes a cytosolic GS gene, GS21, which is different from GS15. In parallel, a number of cDNA clones encoding cytosolic GS were isolated using the coding region of pGS20 as a probe (pGS20 is a cDNA clone which corresponds to a transcript of the GS15 gene). Two new full-length cDNAs designated pGS34 and pGS38 were isolated and sequenced. In the 5' non-coding region a strong homology was found between the two clones and the GS21 gene. However, none of these sequences were identical, which suggests that there are at least three members in this group of genes. In order to determine their relative levels of transcription, specific sequences from pGS34, pGS38 and GS21 were used in an RNAse protection assay. This experiment clearly showed that GS21 and the gene encoding pGS38 are specifically expressed in young or mature nodules, whereas the gene encoding pGS34 is highly transcribed in nodules and constitutively expressed at a lower level in other soybean organs. In order to further analyse the molecular mechanisms controlling GS21 transcription, different fragments of the promoter region were fused to the Escherichia coli reporter gene encoding P-glucuronidase (GUS) and the constructs were introduced into Lotus corniculatus via Agrobacterium rhizogenes-mediated transformation. Analysis of GUS activity showed that the GS21 promoter-GUS constructs were expressed in the vasculature of all vegetative organs. This result is discussed in relation to species-specific metabolic and developmental characteristics of soybean and Lotus. [References: 50]
机译:从大豆基因组文库中分离出DNA片段,该片段包含与GS15 5'区域(编码大豆胞质谷氨酰胺合成酶的基因)杂交的序列。该基因组克隆的作图和部分序列分析表明,它编码一个与GS15不同的胞质GS基因GS21。平行地,使用pGS20的编码区作为探针分离了许多编码胞质GS的cDNA克隆(pGS20是与GS15基因的转录物相对应的cDNA克隆)。分离并测序了两个新的全长cDNA,命名为pGS34和pGS38。在5'非编码区中,在两个克隆和GS21基因之间发现了强同源性。但是,这些序列都不相同,这表明这组基因中至少有三个成员。为了确定它们的相对转录水平,将来自pGS34,pGS38和GS21的特定序列用于RNA酶保护测定中。该实验清楚地表明,GS21和编码pGS38的基因在幼小或成熟结节中特异性表达,而编码pGS34的基因在结节中高度转录,并在其他大豆器官中低水平组成性表达。为了进一步分析控制GS21转录的分子机制,将启动子区域的不同片段融合到编码P-葡萄糖醛酸酶(GUS)的大肠杆菌报告基因上,并通过发根农杆菌介导的转化将构建体引入Lotus corniculatus。 GUS活性的分析表明,GS21启动子-GUS构建体在所有营养器官的脉管系统中表达。讨论了有关大豆和莲花的特定物种代谢和发育特性的结果。 [参考:50]

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