Mishra Smrati, Bansal Shilpi, Mishra Bhawana, Sangwan Rajender Singh, Jadaun Jyoti Singh, Sangwan Neelam S
Department of Metabolic and Structural Biology, CSIR-Central Institute of Medicinal and Aromatic Plants (CSIR-CIMAP), P.O. CIMAP, Lucknow, India.
Center of Innovative and Applied Bioprocessing (CIAB) (A National Institute under Department of Biotechnology, Government of India), C-127, Phase-8, Industrial Area, S.A.S. Nagar, Mohali, Punjab, India.
PLoS One. 2016 Feb 26;11(2):e0149691. doi: 10.1371/journal.pone.0149691. eCollection 2016.
Withania somnifera Dunal, is one of the most commonly used medicinal plant in Ayurvedic and indigenous medicine traditionally owing to its therapeutic potential, because of major chemical constituents, withanolides. Withanolide biosynthesis requires the activities of several enzymes in vivo. Cycloartenol synthase (CAS) is an important enzyme in the withanolide biosynthetic pathway, catalyzing cyclization of 2, 3 oxidosqualene into cycloartenol. In the present study, we have cloned full-length WsCAS from Withania somnifera by homology-based PCR method. For gene function investigation, we constructed three RNAi gene-silencing constructs in backbone of RNAi vector pGSA and a full-length over-expression construct. These constructs were transformed in Agrobacterium strain GV3101 for plant transformation in W. somnifera. Molecular and metabolite analysis was performed in putative Withania transformants. The PCR and Southern blot results showed the genomic integration of these RNAi and overexpression construct(s) in Withania genome. The qRT-PCR analysis showed that the expression of WsCAS gene was considerably downregulated in stable transgenic silenced Withania lines compared with the non-transformed control and HPLC analysis showed that withanolide content was greatly reduced in silenced lines. Transgenic plants over expressing CAS gene displayed enhanced level of CAS transcript and withanolide content compared to non-transformed controls. This work is the first full proof report of functional validation of any metabolic pathway gene in W. somnifera at whole plant level as per our knowledge and it will be further useful to understand the regulatory role of different genes involved in the biosynthesis of withanolides.
印度人参(Withania somnifera Dunal)是阿育吠陀医学和传统本土医学中最常用的药用植物之一,因其具有治疗潜力,主要化学成分是睡茄内酯。睡茄内酯的生物合成在体内需要多种酶的参与。环阿屯醇合酶(CAS)是睡茄内酯生物合成途径中的一种重要酶,催化2,3-氧化角鲨烯环化生成环阿屯醇。在本研究中,我们通过基于同源性的PCR方法从印度人参中克隆了全长WsCAS基因。为了研究基因功能,我们构建了三个基于RNAi载体pGSA骨架的RNAi基因沉默构建体和一个全长过表达构建体。这些构建体被转化到农杆菌菌株GV3101中,用于印度人参的植物转化。对推定的印度人参转化体进行了分子和代谢物分析。PCR和Southern杂交结果表明这些RNAi和过表达构建体已整合到印度人参基因组中。qRT-PCR分析表明,与未转化对照相比,稳定转基因沉默的印度人参株系中WsCAS基因的表达显著下调,HPLC分析表明沉默株系中睡茄内酯含量大幅降低。与未转化对照相比,过表达CAS基因的转基因植物显示出更高水平的CAS转录本和睡茄内酯含量。据我们所知,这项工作是关于印度人参中任何代谢途径基因在全株水平上功能验证的首个完整证据报告,它将有助于进一步了解参与睡茄内酯生物合成的不同基因的调控作用。