茶树己糖激酶基因CsHXK2的启动子克隆及表达特性分析
李娜娜1(
), 刘莹1,2, 张豪杰1, 王璐1, 郝心愿1, 张伟富1, 王玉春1, 熊飞1,3, 杨亚军1,*(), 王新超1,*()
), 刘莹1,2, 张豪杰1, 王璐1, 郝心愿1, 张伟富1, 王玉春1, 熊飞1,3, 杨亚军1,*(), 王新超1,*()
Promoter cloning and expression analysis of the hexokinase gene CsHXK2 in tea plant (Camellia sinensis)
LI Na-Na1(), LIU Ying1,2, ZHANG Hao-Jie1, WANG Lu1, HAO Xin-Yuan1, ZHANG Wei-Fu1, WANG Yu-Chun1, XIONG Fei1,3, YANG Ya-Jun1,*(), WANG Xin-Chao1,*()
), LIU Ying1,2, ZHANG Hao-Jie1, WANG Lu1, HAO Xin-Yuan1, ZHANG Wei-Fu1, WANG Yu-Chun1, XIONG Fei1,3, YANG Ya-Jun1,*(), WANG Xin-Chao1,*()
图2. 茶树CsHXK2蛋白亚细胞定位
A~C和H~K: 35S::sGFP; D~G: 35S::CsHXK2::sGFP; L~O: 35S::CsHXK2-cTP::sGFP。A, D, H, L: GFP绿色荧光信号; E: 叶绿素自发荧光; I, M: 细胞核RFP红色荧光信号; B, F, J, N: 明场; C, G, K, O: 信号融合。
Fig. 2. Subcellular localization of CsHXK2 protein in the tea plant
A-C and H-K: 35S::sGFP; D-G: 35S::CsHXK2::sGFP; L-O: 35S::CsHXK2-cTP::sGFP. A, D, H, L: GFP green fluorescent signal; E: chlorophyll autofluorescence; I, M: RFP red fluorescent signal of nucleus; B, F, J, N: bright field; C, G, K, O: merged signal.
