Sherpa Tsheten, Jha Deepak Kumar, Kumari Khushbu, Chanwala Jeky, Dey Nrisingha
Division of Plant Biotechnology, Institute of Life Sciences, NALCO Square, Chandrasekharpur, Bhubaneswar, Odisha, 751023, India.
Regional Centre for Biotechnology, National Capital Region Biotech Science Cluster, Faridabad, Haryana (NCR Delhi), 121001, India.
Planta. 2023 Jan 18;257(2):40. doi: 10.1007/s00425-023-04066-7.
We characterized an efficient chimeric sub-genomic transcript promoter from Horseradish Latent Virus, FHS4, active in both dicot and monocot plants, and it could be a potential tool for plant biotechnology. Plant pararetroviruses are a rich source of novel plant promoters widely used for biotechnological applications. Here, we comprehensively characterized a unique sub-genomic transcript (Sgt) promoter of Horseradish Latent Virus (HRLV) and identified a fragment (HS4; - 340 to + 10; 351 bp) that showed the highest expression of reporter genes in both transient and transgenic assays as evidenced by biochemical, histochemical GUS reporter assay and transcript analysis of uidA gene by qRT-PCR. Phylogenetic analysis showed that the HSgt promoter was closely related to the sub-genomic promoter of the Cauliflower Mosaic Virus (CaMV19S). We found that the as-1 element and W-box played an important role in the transcriptional activity of the HS4 promoter. Furthermore, the HS4 promoter was also induced by salicylic acid. Alongside, we enhanced the activity of the HS4 promoter by coupling the enhancer region from Figwort Mosaic Virus (FMV) promoter to the upstream region of it. This hybrid promoter FHS4 was around 1.1 times stronger than the most commonly used promoter, 35S (Cauliflower Mosaic Virus full-length transcript promoter), and was efficient in driving reporter genes in both dicot and monocot plants. Subsequently, transgenic tobacco plants expressing an anti-microbial peptide BrLTP2.1 (Brassica rapa lipid transport protein 2.1), under the control of the FHS4 promoter, were developed. The in vitro anti-fungal assay revealed that the plant-derived BrLTP2.1 protein driven by an FHS4 promoter manifested increased resistance against an important plant fungal pathogen, Alternaria alternata. Finally, we concluded that the FHS4 promoter can be used as an alternative to the 35S promoter and has a high potential to become an efficient tool in plant biotechnology.
我们鉴定了一种来自辣根潜隐病毒的高效嵌合亚基因组转录启动子FHS4,它在双子叶植物和单子叶植物中均有活性,可能成为植物生物技术的一个潜在工具。植物类逆转录病毒是新型植物启动子的丰富来源,被广泛用于生物技术应用。在此,我们全面鉴定了辣根潜隐病毒(HRLV)独特的亚基因组转录本(Sgt)启动子,并鉴定出一个片段(HS4;-340至+10;351 bp),该片段在瞬时和转基因试验中均显示出报告基因的最高表达,这通过生化、组织化学GUS报告基因检测以及通过qRT-PCR对uidA基因的转录分析得以证明。系统发育分析表明,HSgt启动子与花椰菜花叶病毒(CaMV19S)的亚基因组启动子密切相关。我们发现,as-1元件和W-box在HS4启动子的转录活性中起重要作用。此外,HS4启动子也受水杨酸诱导。同时,我们通过将玄参花叶病毒(FMV)启动子的增强子区域与HS4启动子的上游区域偶联来增强其活性。这种杂交启动子FHS4比最常用的启动子35S(花椰菜花叶病毒全长转录启动子)强约1.1倍,并且在双子叶植物和单子叶植物中驱动报告基因均很高效。随后,培育了在FHS4启动子控制下表达抗微生物肽BrLTP2.1(甘蓝型油菜脂质转运蛋白2.1)的转基因烟草植株。体外抗真菌试验表明,由FHS4启动子驱动产生的植物源BrLTP2.1蛋白对重要的植物真菌病原体链格孢表现出增强的抗性。最后,我们得出结论,FHS4启动子可作为35S启动子的替代品,并且极有可能成为植物生物技术中的一种有效工具。