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拟南芥转录因子CBF1和CBF4基因的克隆与序列分析
引用本文:徐春波,王勇,杨志如,赵海霞,李兴酉. 拟南芥转录因子CBF1和CBF4基因的克隆与序列分析[J]. 生物技术通报, 2010, 0(2)
作者姓名:徐春波  王勇  杨志如  赵海霞  李兴酉
作者单位:1. 中国农业科学院草原研究所,呼和浩特,010010
2. 内蒙古农业大学生态环境学院,呼和浩特,010018
3. 内蒙古鄂尔多斯市水利勘测设计院,东胜,017000
基金项目:中央级公益性科研院所基本科研业务费专项资会资助项目 
摘    要:利用聚合酶链式反应技术(PCR)从拟南芥(Arabidopsis thaliana)植株中扩增出CBF1和CBF4基因,并将其连接到pGEM-Tvector载体上。PCR和酶切鉴定后进行基因测序,结果表明所克隆的CBF1和CBF4基因序列与GenBank中基因序列同源性分别可达99.84%和99.41%,说明这两个片段确为拟南芥CBF1和CBF4基因。

关 键 词:拟南芥PCR  克隆

Cloning and Sequences Analysis of Transcription Factor CBF1 and CBF4 Gene in Arabidopsis thaliana
Xu Chunbo,Wang Yong,Yang Zhiru,Zhao Haixia,Li Xingyou. Cloning and Sequences Analysis of Transcription Factor CBF1 and CBF4 Gene in Arabidopsis thaliana[J]. Biotechnology Bulletin, 2010, 0(2)
Authors:Xu Chunbo  Wang Yong  Yang Zhiru  Zhao Haixia  Li Xingyou
Affiliation:Xu Chunbo1 Wang Yong2 Yang Zhiru3 Zhao Haixia1 Li Xingyou1(1Grassl, Research Institute of Chinese Academy of Agricultural Sciences,Huhhot 010010,2College of Ecology , Environment Inner Mongolia Agricultural University,Huhhot 010018,3 Water Conservancy Survey , Design Institute in Erdos City,Dongsheng 017000)
Abstract:CBF1 and CBF4 genes were obtained by PCR technique from the plants of Arabidopsis thaliana and then connected those into the pGEM-T vector.PCR,Restriction enzyme digestion and Sequencing results showed that the cloned gene sequences of CBF1 and CBF4 have highly homologous with GenBank,reached 99.84%,99.41% Respectively.Thus,the two fragments were proved as CBF1 and CBF4 gene fragments
Keywords:CBF1  CBF4  CBF1  CBF4  Arabidopsis thaliana  PCR  Clone
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