烟草PR3b转录后剪切元件NRSE1与GUS融合表达后的可变剪切
赵雪1,王锋2,王文静1,刘晓峰1,卞士权1,刘艳华1,刘新民1,杜咏梅1,张忠锋1,张洪博1(
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Splicing Property Analyses of the NRSE1 Element from Tobacco PR3b mRNA After Fusion Expression with GUS Gene
ZHAO Xue1,WANG Feng2,WANG WenJing1,LIU XiaoFeng1,BIAN ShiQuan1,LIU YanHua1,LIU XinMin1,DU YongMei1,ZHANG ZhongFeng1,ZHANG HongBo1()
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图1. NRSE1元件与GUS融合载体的构建示意图
A：PR3b示意图以及可变剪切区65 bp碱基序列,剪切的第1个与后64个碱基间有4个碱基间隔;B：NRSE1元件与GUS的融合表达载体结构示意图
Fig. 1. Schematic diagram of vector construction for the fusion of NRSE1 element and GUS gene
A: The diagram of PR3b gene and the alternative splicing region, and the first spliced base are separated by 4 bases from the left 64 bases; B: Structural diagram of the vector expressing the fusion of NRSE1 element and GUS gene
