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周文平, 王怀琴, 郭晓荣, 杨新兵, 化文平, 曹晓燕. 丹参bHLH转录因子基因SmMYC2的克隆和表达分析[J]. 植物科学学报, 2016, 34(2): 246-254. DOI: 10.11913/PSJ.2095-0837.2016.20246
引用本文: 周文平, 王怀琴, 郭晓荣, 杨新兵, 化文平, 曹晓燕. 丹参bHLH转录因子基因SmMYC2的克隆和表达分析[J]. 植物科学学报, 2016, 34(2): 246-254. DOI: 10.11913/PSJ.2095-0837.2016.20246
ZHOU Wen-Ping, WANG Huai-Qin, GUO Xiao-Rong, YANG Xin-Bing, HUA Wen-Ping, CAO Xiao-Yan. Cloning and Expression Analysis of SmMYC2, a bHLH Transcription Factor Gene from Salvia miltiorrhiza Bunge[J]. Plant Science Journal, 2016, 34(2): 246-254. DOI: 10.11913/PSJ.2095-0837.2016.20246
Citation: ZHOU Wen-Ping, WANG Huai-Qin, GUO Xiao-Rong, YANG Xin-Bing, HUA Wen-Ping, CAO Xiao-Yan. Cloning and Expression Analysis of SmMYC2, a bHLH Transcription Factor Gene from Salvia miltiorrhiza Bunge[J]. Plant Science Journal, 2016, 34(2): 246-254. DOI: 10.11913/PSJ.2095-0837.2016.20246

丹参bHLH转录因子基因SmMYC2的克隆和表达分析

Cloning and Expression Analysis of SmMYC2, a bHLH Transcription Factor Gene from Salvia miltiorrhiza Bunge

  • 摘要: MYC2是植物茉莉酸类激素响应途径中的核心转录因子,在植物防御反应、次生代谢调控及生长发育过程中均有重要的调控作用。基于丹参转录组和基因组survey序列,本研究克隆了丹参转录因子MYC2的基因序列,并命名为SmMYC2 (GenBank No. KJ945636)。SmMYC2基因的cDNA序列长度为1910 bp,开放阅读框(ORF)的长度为1809 bp,编码 602个氨基酸,无内含子;该基因编码蛋白与烟草、番茄等植物的 MYC2蛋白具有较高的同源性;SmMYC2蛋白无跨膜结构域、信号肽等结构。实时荧光定量PCR检测结果显示,SmMYC2在丹参的根、茎、叶、花中均有表达,并且在根和茎中的表达量更高;此外,该基因表达受茉莉酸甲酯、光和机械损伤的诱导,但受赤霉素的抑制。本实验结果为进一步探讨SmMYC2基因在丹参中的生物学功能奠定了基础。

     

    Abstract: MYC2 is a core transcription factor in the response procedure of jasmonic acid hormones. It plays an important role in regulating plant defense responses, secondary metabolism and growth and development processes. Based on Salvia miltiorrhiza Bunge transcriptomes and genome survey sequences, the MYC2 gene transcription factor in S. miltiorrhiza was cloned and named SmMYC2 (GenBank accession number:KJ945636). The cDNA sequence length of SmMYC2 was 1910 bp with no introns, and the open reading frame (ORF)was 1809 bp, encoding 602 amino acids. Moreover, SmMYC2 contained no membrane-spanning domains or signal peptides, and had high homology with MYC2 of tobacco and tomato. Quantitative real-time PCR analysis showed that SmMYC2 was expressed in the roots, stems, leaves and flowers of S. miltiorrhiza, with the highest levels of expression observed in the roots and stems. In addition, the expression of SmMYC2 could be induced by methyl jasmonate, light and wounding, but could be repressed by gibberellin. The present study will be helpful for further functional research of SmMYC2 in S. miltiorrhiza.

     

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