小麦TaWRKY44 基因的克隆、表达分析及功能鉴定
王瑞1,2,**, 吴华玲3,**, 王会芳1,2, 黄珂1,2, 霍春艳1,2, 倪中福1,2, 孙其信1,2,*

Cloning, Characterization, and Functional Analysis ofTaWRKY44 Gene from Wheat
WANG Rui1,2,**, WU Hua-Ling3,**, WANG Hui-Fang1,2, HUANG Ke1,2, HUO Chun-Yan1,2, NI Zhong-Fu1,2, SUN Qi-Xin1,2,*
图 3 TaWRKY44 的组织表达特异性A叶片表达模式B及低温C和干旱胁迫D表达响应 1: 授粉后12 d的种子; 2: 分蘖盛期的分蘖节; 3: 分蘖盛期的分蘖叶; 4: 分蘖盛期的分蘖根。5: 幼叶; 6: 开花期叶片; 7: 衰老叶片。8: 室温 30 min; 9: 3 ℃ 30 min; 10: 室温 60 min; 11: 3 ℃ 60 min。12: H 2 O 2 h; 13: 20% PEG 2 h; 14: H 2 O 4 h; 15: 20%PEG 4 h。
Fig . 3 Tissue-specific expression of TaWRKY44 A expression patterns of leaves B and low temperature C and drought stress D expression in response 1: seeds of 12 days after pollination; 2: inter-node at tillering stage; 3: leaves at tillering stage; 4: root at tillering stage. 5: young leaves; 6: leaves at flowing stage; 7: aged leaves. 8: room temperature for 30 min; 9: 3 °C for 30 min; 10: room temperature for 60 min; 11: 3 °C for 60 min. 12: H 2 O for 2 h; 13: 20% PEG treatment for 2 h; 14: H 2 O for 4 h; 15: 20% PEG for 4 h.