毛竹不同截短U3启动子的克隆及表达分析
凡惠金1,2,金康鸣1,卓仁英1,乔桂荣1,*(
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Cloning and Expression Analysis of Different Truncated U3 Promoters in Phyllostachys edulis
Huijin Fan1,2,Kangming Jin1,Renying Zhuo1,Guirong Qiao1,*()
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图5. 不同截短PeU3启动子驱动LUC在烟草叶片中的瞬时表达
(A), (B) PeU3启动子在烟草叶片中的瞬时表达LUC荧光图; (C) PeU3启动子在烟草叶片中的瞬时表达LUC相对活性(每个实验均设4个生物学重复。* 表示Duncan法检测时在P<0.05水平差异显著); CPS: 荧光强度
Figure 5. LUC expression driven by different truncated PeU3 promoters in the leaves of Nicotiana benthamiana
(A), (B) Transient expression LUC assays illustrating the activation of PeU3 promoter in leaves of N. benthamiana; (C) The quantification of the relative luminescence intensities (In each experiment, four biological replications were performed with quanti?cation. Asterisk above the bars denote significant differences determined by the Duncan’s test, P<0.05); CPS: Luminescence intensity
