陈江, 唐小慧, 任超翔, 陈骁, 何雯, 张思源, 吴清华, 裴瑾. 红花MYB转录因子基因克隆及表达分析J. 药学学报, 2018,53(1): 141-146. doi: 10.16438/j.0513-4870.2017-0614
引用本文: 陈江, 唐小慧, 任超翔, 陈骁, 何雯, 张思源, 吴清华, 裴瑾. 红花MYB转录因子基因克隆及表达分析J. 药学学报, 2018,53(1): 141-146. doi: 10.16438/j.0513-4870.2017-0614
CHEN Jiang, TANG Xiao-hui, REN Chao-xiang, CHEN Xiao, HE Wen, ZHANG Si-yuan, WU Qing-hua, PEI Jin. Cloning and expression analysis of MYB transcription factor genes in safflowerJ. Acta Pharmaceutica Sinica, 2018,53(1): 141-146. doi: 10.16438/j.0513-4870.2017-0614
Citation: CHEN Jiang, TANG Xiao-hui, REN Chao-xiang, CHEN Xiao, HE Wen, ZHANG Si-yuan, WU Qing-hua, PEI Jin. Cloning and expression analysis of MYB transcription factor genes in safflowerJ. Acta Pharmaceutica Sinica, 2018,53(1): 141-146. doi: 10.16438/j.0513-4870.2017-0614

红花MYB转录因子基因克隆及表达分析

Cloning and expression analysis of MYB transcription factor genes in safflower

  • 摘要: 红花是菊科一年生草本植物红花(Carthamus tinctorius L.)的干燥花,为活血化瘀常用中药。黄酮类成分是红花主要有效成分,MYB转录因子广泛参与调控黄酮类成分的合成,对红花MYB转录因子克隆及表达分析为解析红花黄酮类成分的调控机制、调控黄酮类成分的合成具有重要意义。本研究基于在线二代转录组数据,首先利用iTAK软件对MYB转录因子进行注释,设计引物对长片段MYB转录因子基因进行克隆,其次对克隆到的MYB转录因子基因进行序列分析,再次利用实时荧光定量PCR对克隆的MYB转录因子基因表达进行分析。注释筛选得到8个长片段MYB转录因子基因,成功克隆到6个MYB转录因子基因,分别命名为CtMYB-TF1、CtMYB-TF2、CtMYB-TF4、CtMYB-TF5、CtMYB-TF6CtMYB-TF7。序列分析表明,克隆到的6个MYB转录因子基因都具有MYB转录因子核心结构域,其中CtMYB-TF7转录因子同已报道黄酮类成分合成调控因子AtMYBL2及AtMYB12关系较近。表达分析表明,CtMYB-TF5、CtMYB-TF6CtMYB-TF7在根、茎及叶中表达量低,在花中表达量高。研究结果为进一步研究红花黄酮类成分的分子调控奠定基础。

     

    Abstract: Safflower is a dried flower of the annual herbaceous plant safflower (Carthamus tinctorius L.). As a traditional Chinese medicine, it was widely used in the regulation of blood circulation. Flavonoids are the main active ingredients in safflower. MYB transcription factors are involved in the regulation of flavonoids. The cloning and expression analysis of MYB transcription factor genes in safflower is of great significance, not only for clarifying the regulation mechanism of flavonoids biosynthesis in safflower, but also for the artificial regulation of flavonoid biosynthesis in safflower. Based on the transcriptome data, we used iTAK to annotate the MYB transcription factors in safflower. The MYB transcription factors were cloned and their sequences were analyzed. Besides, their expressions were analyzed by a Real-time PCR. In the experiment, eight long fragment MYB transcription factors were screened and six MYB transcription factors was successfully cloned, named CtMYB-TF1, CtMYB-TF2, CtMYB-TF4, CtMYB-TF5, CtMYB-TF6 and CtMYB-TF7, respectively. The six MYB transcription factors had the core domain of MYB transcription factor family, and evolutionary analysis showed that the CtMYB-TF7 transcription factor was closely related to the factors AtMYBL2 and AtMYB12. Expression analysis showed that the expression of CtMYB-TF5, CtMYB-TF6 and CtMYB-TF7 was low in roots, stems and leaves, and was high in the flower. The results provide a foundation for study of mechanism of molecular regulation of safflower flavonoids.

     

/

返回文章
返回