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,*()
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,*()

图5. 茶树CsHXK2基因在不同处理下的表达分析
A: 自然冷驯化; B: 4℃低温及25℃恢复; C: 炭疽菌接种; D: 50 μmol L-1外源GA3处理。柱上标以不同字母表示数据间的显著性差异(P < 0.05)。*表示0.05水平显著; ***表示0.001水平显著。

Fig. 5. Expression analysis of CsHXK2 under different treatments in the tea plant
A: natural cold acclimation; B: 4℃ cold and 25℃ recovery; C: inoculation with Colletotrichum; D: 50 μmol L-1 exogenous GA3. Different letters on the column indicate significant difference between the data (P < 0.05). * indicates significant at the 0.05 probability level; *** indicates significant at the 0.001 probability level.