茶树CsCBF1基因克隆和转录活性分析
CSTR:
作者:
作者单位:

作者简介:

通讯作者:

中图分类号:

基金项目:

国家自然科学基金(30570137);河南省基础与前沿技术研究计划项目(092300410244)


Isolation and Transcription Activation Analysis of the CsCBF1 Gene from Camellia sinensis
Author:
Affiliation:

Fund Project:

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    采用RACE 技术克隆了一个受冷诱导的茶树CBF基因全长cDNA,命名为CsCBF1(GenBank登录号为EU563238)。CsCBF1 cDNA全长序列为1 211 bp,开放阅读框编码259个氨基酸。氨基酸序列分析表明,CsCBF1具有CBF家族典型的保守结构域,与其他植物的CBF具有较高的相似性;与拟南芥、辣椒和橡胶树编码的CBF相似性分别为56%、63%和56%。亚细胞定位结果表明,CsCBF1位于细胞核内。分别将10个CsCBF1缺失突变体与GAL4 DNA结合域融合的结果显示,CsCBF1的羧基末端酸性结构域(第137位氨基酸至259位氨基酸)在酵母中具有转录激活活性。实时定量RT-PCR分析表明,CsCBF1基因受低温的快速诱导表达。

    Abstract:

    The full-length cDNA of a cold-induced CBF gene was cloned from tea (Camellia sinensis),and designated as CsCBF1( GenBank accession No.EU563238) by RACE method.The cDNA was 1 211 bp in length,and contained an open reading frame encoding 259 amino acids.Amino acid sequence alignment showed that CsCBF1 contained all typical conserved motifs of CBF family.CsCBF1 protein was very similar in amino acid sequence to CBFs from other plant species,and showing 56%,63% and 56% amino acid sequence identity to CBFs from Arabidopsis thaliana,Capsicum annuum,and Hevea brasiliensis,respectively.Subcellular location assay indicated that CsCBF1-GFP fusion protein was located in nucleus.When ten deletion mutants of CsCBF1 were fused in-frame to the yeast GAL4 DNA-binding domain,its carboxyl-terminal acidic region (from 137th amino acid to 259th amino acid) could activate the transcription in yeast.Quantitative real-time RT-PCR analysis revealed that CsCBF1 was induced quickly by low temperature.

    参考文献
    相似文献
    引证文献
引用本文

袁红雨,朱小佩,曾 威,等.茶树CsCBF1基因克隆和转录活性分析[J].西北植物学报,2013,33(9):1717-1723

复制
分享
相关视频

文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:
  • 最后修改日期:
  • 录用日期:
  • 在线发布日期: 2013-10-09
  • 出版日期:
文章二维码