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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Development of a salicylic acid inducible minimal sub-genomic transcript promoter from Figwort mosaic virus with enhanced root- and leaf-activity using TGACG motif rearrangement
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Development of a salicylic acid inducible minimal sub-genomic transcript promoter from Figwort mosaic virus with enhanced root- and leaf-activity using TGACG motif rearrangement

机译:利用TGACG基序重排,从Figwort花叶病毒中开发出水杨酸诱导的最小亚基因组转录本启动子,具有增强的根和叶活性

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In Figwort mosaic virus sub-genomic transcript promoter (F-Sgt), function of the TGACG-regulatory motif, was investigated in the background of artificially designed promoter sequences. The 131bp (FS, -100 to +31) long F-Sgt promoter sequence containing one TGACG motif [FS-(TGACG)] was engineered to generate a set of three modified promoter constructs: [FS-(TGACG) 2, containing one additional TGACG motif at 7 nucleotides upstream of the original one], [FS-(TGACG) 3, containing two additional TGACG motifs at 7 nucleotides upstream and two nucleotides downstream of the original one] and [FS-(TGCTG) mu, having a mutated TGACG motif]. EMSA and foot-printing analysis confirmed binding of tobacco nuclear factors with modified TGACG motif/s. The transcription-activation of the GUS gene by the TGACG motif/s in above promoter constructs was examined in transgenic tobacco and Arabidopsis plants and observed that the transcription activation was affected by the spacing/s and number/s of the TGACG motif/s. The FS-(TGACG) 2 promoter showed strongest root-activity compared to other modified and CaMV35S promoters. Also under salicylic acid (SA) stress, the leaf-activity of the said promoter was further enhanced. All above findings were confirmed by real-time and semi-qRT PCR analysis. Taken together, these results clearly demonstrated that the TGACG motif plays an important role in inducing the root-specific expression of the F-Sgt promoter. This study advocates the importance of genetic manipulation of functional cis-motif for amending the tissue specificity of a plant promoter. SA inducible FS-(TGACG) 2 promoter with enhanced activity could be a useful candidate promoter for developing plants with enhanced crop productivity.
机译:在Figwort花叶病毒亚基因组转录子启动子(F-Sgt)中,在人工设计的启动子序列的背景下研究了TGACG调节基序的功能。将含有一个TGACG基序[FS-(TGACG)]的131bp(FS,-100至+31)长的F-Sgt启动子序列进行工程改造,以生成一组三个修饰的启动子构建体:[FS-(TGACG)2,包含一个[FS-(TGACG)3,在原始序列的上游7个核苷酸处有一个额外的TGACG基序],[FS-(TGACG)3,在原始序列的上游7个核苷酸处有两个额外的TGACG基序,在原始序列的一个下游有两个核苷酸]和突变的TGACG主题]。 EMSA和足迹分析证实了烟草核因子与修饰的TGACG基序的结合。在转基因烟草和拟南芥植物中检查了上述启动子构建体中由TGACG基序引起的GUS基因的转录激活,并观察到转录激活受TGACG基序的间隔和/或数目影响。与其他修饰和CaMV35S启动子相比,FS-(TGACG)2启动子显示出最强的根活性。同样在水杨酸(SA)胁迫下,所述启动子的叶活性进一步增强。以上所有发现均通过实时和半定量RT PCR分析得到证实。综上所述,这些结果清楚地表明,TGACG基序在诱导F-Sgt启动子的根特异性表达中起重要作用。这项研究主张功能性顺式基序的基因操作对于修改植物启动子的组织特异性的重要性。具有增强活性的SA诱导型FS-(TGACG)2启动子可能是用于发展具有提高作物生产力的植物的有用候选启动子。

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