Chattopadhyay Anirudha, Jailani A Abdul Kader, Roy Anirban, Mukherjee Sunil Kumar, Mandal Bikash
Advanced Centre for Plant Virology, Division of Plant Pathology, Indian Agricultural Research Institute, New Delhi 110012, India.
Pulses Research Station, Sardarkrushinagar Dantiwada Agricultural University, Sardarkrushinagar 385506, Gujarat, India.
Plants (Basel). 2024 May 19;13(10):1414. doi: 10.3390/plants13101414.
Expanding possibilities for foreign gene expression in cucurbits, we present a novel approach utilising a bipartite vector system based on the cucumber green mottle mosaic virus (CGMMV) genome. Traditional full-length CGMMV vectors face limitations such as a restricted cargo capacity and unstable foreign gene expression. To address these challenges, we developed two 'deconstructed' CGMMV genomes, DG-1 and DG-2. DG-1 features a major internal deletion, resulting in the loss of crucial replicase enzyme domains, rendering it incapable of self-replication. However, a staggered infiltration of DG-1 in CGMMV-infected plants enabled successful replication and movement, facilitating gene-silencing experiments. Conversely, DG-2 was engineered to enhance replication rates and provide multiple cloning sites. Although it exhibited higher replication rates, DG-2 remained localised within infiltrated tissue, displaying trans-replication and restricted movement. Notably, DG-2 demonstrated utility in expressing GFP, with a peak expression observed between 6 and 10 days post-infiltration. Overall, our bipartite system represents a significant advancement in functional genomics, offering a robust tool for foreign gene expression in .
为了拓展葫芦科植物中外源基因表达的可能性,我们提出了一种基于黄瓜绿斑驳花叶病毒(CGMMV)基因组的二分载体系统的新方法。传统的全长CGMMV载体面临着诸如载体容量受限和外源基因表达不稳定等限制。为应对这些挑战,我们开发了两个“解构”的CGMMV基因组,即DG-1和DG-2。DG-1有一个主要的内部缺失,导致关键复制酶结构域的丢失,使其无法自我复制。然而,在CGMMV感染的植物中交错接种DG-1能够成功复制和移动,便于进行基因沉默实验。相反,DG-2经过改造以提高复制率并提供多个克隆位点。尽管DG-2表现出更高的复制率,但它仍局限于接种组织内,表现出反式复制和有限的移动性。值得注意的是,DG-2在表达绿色荧光蛋白(GFP)方面显示出实用性,在接种后6至10天观察到表达峰值。总体而言,我们的二分系统代表了功能基因组学的一项重大进展,为葫芦科植物中的外源基因表达提供了一个强大的工具。