甘蓝型油菜PGK基因的克隆与表达分析
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(31171588);重庆市自然科学基金(cstc2012jjA80010)


Cloning and Expression Analysis of PGK Gene in Brassica napus
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:

    为研究甘蓝型油菜磷酸甘油酸激酶(PGK)基因表达特性,在对拟南芥PGK基因家族生物信息学分析的基础上,通过电子克隆方法获得3个甘蓝型油菜PGK基因(BnPGK1、BnPGK2、BnPGK3)。分别设计特异引物,以甘蓝型油菜雄性不育系09A和保持系09B的cDNA为模板克隆BnPGK基因全长序列。根据获得的cDNA序列设计实时荧光定量特异引物,采用实时荧光定量PCR技术,研究油菜雄性不育系与保持系PGK基因表达差异。结果显示:BnPGK基因在甘蓝型油菜雄性不育系09A和保持系09B的根、茎、叶、花蕾中均有表达,属组成性表达。除茎中的BnPGK3外,BnPGK其它基因在根、茎、叶中的表达均表现为09A高于09B,而在花蕾中均为09B高于09A,BnPGK1和BnPGK3在09B中的表达量是09A中的2倍以上。

    Abstract:

    Three full-length cDNA sequences of PGK genes(BnPGK1,BnPGK2 and BnPGK3) were obtained through electronic cloning method based on bioinformatics analysis of Arabidopsis PGK gene family for the study of Phosphoglycerate kinase(PGK) gene expression characteristics from Brassica napus.Specific primers were designed and cDNA of male sterile line 09A and maintainer line 09B were as templates to clone BnPGK full-length sequences.Real-time fluorescence quantitative specific primers were designed according to the obtained cDNA sequences.The Real-time quantitative analysis was conducted by using Quantitative PCR method.Results showed that the BnPGK genes expressed variously in different tissues,such as root,stem,leaf and bud of 09A and 09B,belong to constitutively expressed.Except BnPGK3 in the stem,the expression of BnPGK other genes of 09A were higher than that of 09B in root,stem and leaf,but the expression of BnPGK genes of 09B were higher than that of 09A and the expression of BnPGK1 and BnPGK3 of 09B was 2 times than that of 09A in bud.

    参考文献
    相似文献
    引证文献
引用本文

郭 楠,赵敬会,高天姝,等.甘蓝型油菜PGK基因的克隆与表达分析[J].西北植物学报,2014,34(11):2188-2193

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: 2014-12-08
  • 出版日期:
文章二维码