植物学报 ›› 2005, Vol. 22 ›› Issue (05): 594-598.

• 技术与方法 • 上一篇    下一篇

拟南芥CHS 基因表达的实时荧光定量PCR 检测

王艳 蒋磊 李韶山   

  1. 1(华南师范大学生命科学学院 广州 510631) 2(暨南大学理工学院环境工程系 广州 510632)
  • 收稿日期:2005-04-26 修回日期:2005-07-29 出版日期:2005-10-30 发布日期:2005-10-30
  • 通讯作者: 李韶山

Quantitative Analysis of CHS Gene Expression in Arabidopsis thaliana by Real-time RT-PCR

WANG Yan JIANG Lei LI Shao-Shan   

  1. 1(College of Life Science, South China Normal University, Guangzhou 510631) 2(College of Science and Engineering, Jinan University, Guangzhou 510632)
  • Received:2005-04-26 Revised:2005-07-29 Online:2005-10-30 Published:2005-10-30
  • Contact: LI Shao-Shan

摘要: 在简要介绍实时荧光定量PCR反应和定量原理的基础上, 采用TaqMan荧光定量PCR技术, 研究了UV-B辐射对拟南芥(Arabidopsis thaliana)CHS(查耳酮合成酶基因)表达的诱导, 获得了与传统Northern杂交一致的结果。实时荧光定量PCR用于基因表达的定量检测, 具有特异性强、自动化程度高、高效快捷, 避免使用放射性同位素, 能同时对多个样品中的起始模板进行准确定量等特点, 因此该方法已逐渐被广泛用于基因表达的定量分析。

Abstract: Fluorescent-based real-time PCR is widely used for quantification of nucleic acids. It is becoming one of the most important techniques for molecular biology and biotechnology.Real-time PCR assay is easy to perform, capable of high throughput, and can combine high sensitivity with reliable specificity. The technique is evolving rapidly with the knowledge of new enzymes, chemistry and instrumentation. The principle of real-time PCR and its application in quantifying plant nucleic acids is reviewed.