He Chaochao, Liang Yue, Chen Runzhou, Shen Yuxiao, Li Runhui, Sun Tingting, Du Xing, Ni Xiaomei, Shang Junzhong, He Yanhong, Bao Manzhu, Luo Hong, Wang Jihua, Liao Pan, Kang Chunying, Yuan Yao-Wu, Ning Guogui
National Key Laboratory for Germplasm Innovation & Utilization of Horticultural Crops, Huazhong Agricultural University, Wuhan 430070, China.
The Institute of Flowers Research, Huazhong Agricultural University, Wuhan 430070, China.
Plant Cell. 2025 Feb 13;37(2). doi: 10.1093/plcell/koae315.
Enhancing the transcriptional activation activity of transcription factors (TFs) has multiple applications in organism improvement, metabolic engineering, and other aspects of plant science, but the approaches remain unclear. Here, we used gene activation assays and genetic transformation to investigate the transcriptional activities of two MYB TFs, PRODUCTION OF ANTHOCYANIN PIGMENT 1 (AtPAP1) from Arabidopsis (Arabidopsis thaliana) and EsMYBA1 from Epimedium (Epimedium sagittatum), and their synthetic variants in a range of plant species from several families. Using anthocyanin biosynthesis as a convenient readout, we discovered that homologous naturally occurring TFs showed differences in the transcriptional activation ability and that similar TFs induced large changes in the genetic program when heterologously expressed in different species. In some cases, shuffling the DNA-binding domains and transcriptional activation domains (ADs) between homologous TFs led to synthetic TFs that had stronger activation potency than the original TFs. More importantly, synthetic TFs derived from MYB, NAC, bHLH, and ethylene-insensitive3-like (EIL) family members containing tandemly repeated ADs had greatly enhanced activity compared to their natural counterparts. These findings enhance our understanding of TF activity and demonstrate that employing tandemly repeated ADs from natural TFs is a simple and widely applicable strategy to enhance the activation potency of synthetic TFs.
增强转录因子(TFs)的转录激活活性在植物改良、代谢工程及植物科学的其他方面有多种应用,但具体方法仍不明确。在此,我们利用基因激活分析和遗传转化,研究了来自拟南芥的两个MYB转录因子花青素色素合成1(AtPAP1)和来自淫羊藿的EsMYBA1及其合成变体在多个科的一系列植物物种中的转录活性。以花青素生物合成作为便捷的检测指标,我们发现同源的天然转录因子在转录激活能力上存在差异,并且相似的转录因子在不同物种中异源表达时会引起遗传程序的巨大变化。在某些情况下,在同源转录因子之间交换DNA结合结构域和转录激活结构域(ADs)会产生比原始转录因子具有更强激活效力的合成转录因子。更重要的是,与天然对应物相比,源自含有串联重复ADs的MYB、NAC、bHLH和乙烯不敏感3样(EIL)家族成员的合成转录因子具有大大增强的活性。这些发现增进了我们对转录因子活性的理解,并证明采用来自天然转录因子的串联重复ADs是增强合成转录因子激活效力的一种简单且广泛适用的策略。