生物技术通报 ›› 2023, Vol. 39 ›› Issue (5): 217-223.doi: 10.13560/j.cnki.biotech.bull.1985.2022-1231

• 研究报告 • 上一篇    下一篇

虎杖转录因子PcMYB2的表达特性和功能分析

姜晴春(), 杜洁, 王嘉诚, 余知和, 王允, 柳忠玉()   

  1. 长江大学生命科学学院,荆州 434025
  • 收稿日期:2022-10-08 出版日期:2023-05-26 发布日期:2023-06-08
  • 通讯作者: 柳忠玉,女,博士,副教授,研究方向:药用植物次生代谢与调控;E-mail: zyliu2004@126.com
  • 作者简介:姜晴春,女,硕士研究生,研究方向:植物分子生物学;E-mail: 2870140725@qq.com
  • 基金资助:
    国家自然科学基金项目(81803670);长江大学校级大学生创新训练计划(2019279)

Expression and Function Analysis of Transcription Factor PcMYB2 from Polygonum cuspidatum

JIANG Qing-chun(), DU Jie, WANG Jia-cheng, YU Zhi-he, WANG Yun, LIU Zhong-yu()   

  1. College of Life Science, Yangtze University, Jingzhou 434025
  • Received:2022-10-08 Published:2023-05-26 Online:2023-06-08

摘要:

对虎杖R2R3-MYB转录因子PcMYB2进行转录活性鉴定和表达特性分析,并在转基因拟南芥和转基因毛状根中进行功能研究。利用酵母单杂交试验分析PcMYB2的转录活性;实时荧光定量PCR(RT-qPCR)技术检测虎杖中PcMYB2的表达模式;DMACA法检测PcMYB2转基因拟南芥和虎杖毛状根中的原花青素含量。酵母单杂试验表明,PcMYB2具有转录激活活性;RT-qPCR结果显示,PcMYB2在虎杖根、茎、叶中均有表达,在叶中表达量最高,并且ABA和H2O2外源处理可诱导叶片中PcMYB2的表达;与野生型拟南芥相比,转基因拟南芥种皮颜色加深,原花青素含量为野生型的1.8倍;与野生型毛状根相比,转基因毛状根DMACA染色更深,原花青素含量为野生型的2.3倍。PcMYB2具有转录激活活性,且促进植物原花青素的生物合成。

关键词: 虎杖, PcMYB2, 转录活性, 表达分析, 原花青素生物合成

Abstract:

This work aims to identify the transcriptional activity and expression profile of PcMYB2, encoding an R2R3-MYB transcription factor from Polygonum cuspidatum, and to evaluate the biological functions of PcMYB2 in transgenic Arabidopsis thaliana plant and transformed P. cuspidatum hairy roots. The yeast one hybrid was used to analyze transcriptional activity. And quantitative real time PCR(RT-qPCR)technique was applied to detect the tissue-specific expression profile of PcMYB2 in P. cuspidatum and its expression pattern in responses to stress treatments. The DMACA method was to determine the contents of proanthocyanidins in PcMYB2-transgenic A. thaliana and P. cuspidatum hairy roots. The yeast one hybrid experiment showed that PcMYB2 had transcriptional activity. The PcMYB2 gene was expressed in the roots, stems and leaves of P. cuspidatum, with the highest expression in the leaves, and the expression of PcMYB2 gene in the leaves was induced after application of ABA or H2O2. Transgenic A. thaliana presented an increase in the pigmentation of mature seed compared with the wild type, and the proanthocyanidins content was 1.8-fold higher than that of the wild type. Staining of the hairy roots with DMACA was darker compared with wild type, and proanthocyanidins content was 2.3-fold higher. Altogether, this study reveals that PcMYB2 has transcriptional activity and may promote the proanthocyanidins biosynthesis.

Key words: Polygonum cuspidatum Sieb. et Zucc., PcMYB2, transcriptional activity, expression analysis, proanthocyanidins biosynthesis