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白桦BpGT14基因启动子克隆及表达活性分析
  • ISSN号:1000-1522
  • 期刊名称:《北京林业大学学报》
  • 时间:0
  • 分类:S718.43[农业科学—林学] S792.153[农业科学—林木遗传育种;农业科学—林学]
  • 作者机构:东北林业大学生命科学学院林木遗传育种国家重点实验室
  • 相关基金:中央高校基本科研业务费专项(2572014DA04); 国家自然科学基金项目(31200463,J1210053)
中文摘要:

本文利用Site Finding-PCR方法克隆了白桦BpGT14基因起始密码子ATG上游2 169 bp序列,并通过PLACE启动子预测工具对其进行元件分析。结果表明,该启动子片段含有启动子核心元件及多种逆境及激素响应元件,同时具有植物苯丙烷及木质素生物合成的MYB类转录因子的重要结合基序。研究选取了其中含有启动子核心元件的1 156 bp片段构建了pBpGT14∷GUS植物表达载体,利用农杆菌侵染的方法将pBpGT14∷GUS报告基因瞬时转化烟草植株,鉴定该启动子在烟草中的表达活性及对非生物胁迫和激素的响应模式。对转基因烟草植株进行GUS染色,结果表明该启动子具有启动活性,且在茎段处活性较高;进一步分析非生物胁迫对烟草中GUS酶活性的影响,表明该启动子对ABA、NaCl、PEG及高温处理均有明显响应,且对于NaCl及PEG处理响应迅速。为了更好的鉴定白桦BpGT14基因启动子在白桦细胞中的启动活性及响应模式,本文构建了pBpGT14∷GFP载体并瞬时转化白桦茎段悬浮细胞,进行研究。GFP转录水平分析结果与GUS酶活性结果基本一致,但其中部分时间点仍存在差异。选取PEG处理3、6、12及24 h的转GFP基因白桦茎段悬浮细胞,在显微镜下观察其绿色荧光蛋白,以此揭示该启动子对干旱的响应模式。结果表明,该启动子在白桦茎段悬浮细胞中启动了GFP的表达,在处理初期(3 h),荧光效果明显;随着处理时间的增加,细胞脱水明显,且在细胞壁表现高亮度荧光。

英文摘要:

We cloned a 2 169 bp promoter sequence of BpGT14 gene from birch genomic DNA using the method of Site Finding-PCR. The promoter sequence was analyzed by PLACE,and the result showed that this fragment contained promoter core elements and some elements which can respond to abiotic stress and hormones. Meanwhile, two important MYB transcription factor binding elements were found which regulate phenylpropanoid and lignin biosynthesis. To study the promoter activity,a 1 156 bp fragment was chosen to construct p BpGT14∷GUS plant expression vector and transformed into tobacco. GUS staining proved that the promoter had high activity in stem segments. When the tobacco was treated with GA and H2O2 at 4 ℃,the promoter had no significant response and the enzyme activity had a downward trend. In contrast,the promoter activity was significantly increased by ABA,Na Cl,PEG and 37 ℃ treatment.Further transformation of birch cells using p BpGT14 ∷ GFP plant expression vector indicated that the promoter had a similar response pattern to that of tobacco treated with abiotic stress and hormone except for a few time points. As the promoter was significantly and quickly responsive to drought stress,we have observed the GFP fluorescence protein in birch stem segments suspension cells transformed by GFP for 3,6,12 and 24 h with PEG treatment. The results showed that BpGT14 promoter had activity in birch stem segments suspension cells and fluorescence can be observed in the suspension cells,especially in cell walls. Successful implementation of this study has important significance for analysis of gene regulation and function. Meanwhile,it provides a theoretical basis for gene promoter function studies of other woody plants.

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期刊信息
  • 《北京林业大学学报》
  • 北大核心期刊(2011版)
  • 主管单位:中华人民共和国教育部
  • 主办单位:北京林业大学
  • 主编:尹伟伦
  • 地址:北京市海淀区清华东路35号
  • 邮编:100083
  • 邮箱:bldxeb@bjfu.edu.cn
  • 电话:010-62337673
  • 国际标准刊号:ISSN:1000-1522
  • 国内统一刊号:ISSN:11-1932/S
  • 邮发代号:82-304
  • 获奖情况:
  • 中国期刊方阵“双效”期刊
  • 国内外数据库收录:
  • 俄罗斯文摘杂志,美国化学文摘(网络版),英国农业与生物科学研究中心文摘,美国剑桥科学文摘,英国动物学记录,日本日本科学技术振兴机构数据库,中国中国科技核心期刊,中国北大核心期刊(2004版),中国北大核心期刊(2008版),中国北大核心期刊(2011版),中国北大核心期刊(2014版),中国北大核心期刊(2000版)
  • 被引量:30004