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首页> 外文期刊>Plant Science >STRUCTURE AND RFLP MAPPING OF A RICE SUCROSE PHOSPHATE SYNTHASE (SPS) GENE THAT IS SPECIFICALLY EXPRESSED IN THE SOURCE ORGAN
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STRUCTURE AND RFLP MAPPING OF A RICE SUCROSE PHOSPHATE SYNTHASE (SPS) GENE THAT IS SPECIFICALLY EXPRESSED IN THE SOURCE ORGAN

机译:在源器官中特异性表达的水稻蔗糖磷酸合成酶(SPS)基因的结构和RFLP定位

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摘要

A rice sucrose phosphate synthase (SPS) gene was isolated and mapped on chromosome 1, based upon RFLPs be tween a japonica line 'FL134' and an indica cultivar 'Kasalath'. This gene consisted of 12 exons with 11 introns. In the exon 1, an additional sequence occurred bearing an insertion encoding 24 glycine residues when it was compared with the spinach one. Although the structure of this region possessed the consensus intron borders, its size was only 48 bp and it occurred with neither breakage of open reading frame nor shift of the reading frame. The deduced amino acid sequence of the rice SPS showed a high degree of homology to the known ones. Sites for modification by kinase/phosphatase and for binding with UDP-glucose were highly conserved. No typical promoter sequences were found upstream of the coding region, suggesting that function of the promoter of this gene is weak, although further upstream of the coding region, sequences similar to the promoter and light-responsive elements were found. Expression of this gene was detected only in the leaves, suggesting that this gene is specifically expressed in the source organs. Level of expression was extremely low, reflecting weakness of its promoter activity.
机译:水稻蔗糖磷酸合酶(SPS)基因被分离并定位在1号染色体上,基于粳稻“ FL134”和in稻“ Kasalath”之间的RFLP。该基因由12个外显子和11个内含子组成。在第一个外显子中,与菠菜相比,出现了一个附加序列,带有一个编码24个甘氨酸残基的插入序列。尽管该区域的结构具有共有的内含子边界,但其大小仅为48 bp,并且既没有开放阅读框的断裂也没有阅读框的移位。推导出的水稻SPS氨基酸序列与已知序列具有高度的同源性。激酶/磷酸酶修饰位点和与UDP-葡萄糖结合的位点高度保守。在编码区的上游没有发现典型的启动子序列,这表明该基因的启动子的功能很弱,尽管在编码区的更上游,发现了与启动子和光响应元件相似的序列。仅在叶子中检测到该基因的表达,表明该基因在源器官中特异性表达。表达水平极低,反映了其启动子活性的弱点。

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