茶树己糖激酶基因CsHXK2的启动子克隆及表达特性分析
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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,*( )
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Promoter cloning and expression analysis of the hexokinase gene CsHXK2 in tea plant (Camellia sinensis)
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LI Na-Na 1( ), LIU Ying 1,2, ZHANG Hao-Jie 1, WANG Lu 1, HAO Xin-Yuan 1, ZHANG Wei-Fu 1, WANG Yu-Chun 1, XIONG Fei 1,3, YANG Ya-Jun 1,*( ), WANG Xin-Chao 1,*( )
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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。
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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.
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