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论文摘要

茎瘤芥BjMYB1基因的克隆、表达与遗传转化研究

Molecular cloning, expression and genetic transformation of BjMYB1 gene in tumourous stem mustard (Brassica juncea var. tumida Tsen et Lee)

作者:王微娜(重庆邮电大学生物信息学院; 河南大学生命科学学院/棉花生物学国家重点实验室);孙全(重庆邮电大学生物信息学院; 河南大学生命科学学院/棉花生物学国家重点实验室);蔡应繁(重庆邮电大学生物信息学院; 河南大学生命科学学院/棉花生物学国家重点实验室);江怀仲(重庆邮电大学生物信息学院);杨璨(重庆邮电大学生物信息学院);何晓红(重庆邮电大学生物信息学院);牟军(重庆邮电大学生物信息学院)

Author:WANG Wei-Na(College of Bioinformation, Chongqing University of Posts and Telecommunications; State Key Laboratory of Cotton Biology, College of Life Science, Henan University);SUN Quan(College of Bioinformation, Chongqing University of Posts and Telecommunications; State Key Laboratory of Cotton Biology, College of Life Science, Henan University);CAI Ying-Fan(College of Bioinformation, Chongqing University of Posts and Telecommunications; State Key Laboratory of Cotton Biology, College of Life Science, Henan University);JIANG Huai-Zhong(College of Bioinformation, Chongqing University of Posts and Telecommunications);YANG Can(College of Bioinformation, Chongqing University of Posts and Telecommunications);HE Xiao-Hong(College of Bioinformation, Chongqing University of Posts and Telecommunications);MOU Jun(College of Bioinformation, Chongqing University of Posts and Telecommunications)

收稿日期:2015-03-05          年卷(期)页码:2016,53(4):888-894

期刊名称:四川大学学报: 自然科学版

Journal Name:Journal of Sichuan University (Natural Science Edition)

关键字:茎瘤芥;MYB转录因子;亚细胞定位;遗传转化

Key words:Brassica juncea var. tumida Tsen et Lee; MYB transcript factor; subcellular localization; genetic transformation

基金项目:国家自然科学基金

中文摘要

MYB转录因子广泛地参与了植物细胞分化、细胞周期的调节,激素和环境因子应答等过程。本研究根据茎瘤芥转录组测序筛选获得了一个MYB基因片段。通过RACE的方法,克隆得到了两条长度分别为975bp和864bp的全长序列,分析发现可能为茎瘤芥MYB基因的两种不同选择性拼接形式,并命名为BjMYB1-3和BjMYB1-4。对BjMYB1-3和BjMYB1-4做组织表达分析,发现这两个转录本在茎中特异表达。针对BjMYB1-3和BjMYB1-4的亚细胞定位分析,显示BjMYB1-4定位于细胞核,BjMYB1-3部分定位于细胞核。构建BjMYB-3和BjMYB1-4的超表达载体转化拟南芥,结果显示超表达转化的植株会使拟南芥提前抽薹和开花,说明BjMYB1-3和BjMYB1-4在植株的生长发育过程中起着一定作用,为进一步阐明茎瘤芥BjMYB1基因的功能奠定了基础。

英文摘要

The MYB transcript factors widely involves in many important physiological processes in plants, including cell differentiation, cell cycle regulation, hormone and environmental stress responses, secondary metabolism, and tissue morphogenesis. A fragment of MYB gene was figured out based on transcription analysis of different periods of stem swelling. Two cDNA sequences, 975bp and 864bp, were cloned by rapid amplification of cDNA ends. Moreover, these two genes, namely BjMYB1-3 and BjMYB1-4, may be the two different alternative splicing patterns of BjMYB1 gene. By analysis the tissue expression of BjMYB1-3 and BjMYB1-4, they were particularly expressed in stem. An analysis of the subcellular localisation of the proteins indicated that BjMYB1-4 was present only in the nucleus, while the BjMYB1-3 GFP fusion protein was partially localised to the nucleus. By constructing the overexpression vector of BjMYB1-3 and BjMYB1-4 and conducting the genetic transformation of Arabidopsis thaliana, we found that the plants which were transformated taked out and flowered in advance. The result showed that these two transcripts played an important role in the growth and development of plant. The result of study laid the foundation of clarifying the function of MYB gene.

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