Mahmood Muhammad Arslan, Sajjad Muhammad Waseem, Imran Ifrah, Naqvi Rubab Zahra, Amin Imran, Shafiq Muhammad, Aslam Muhammad Qasim, Mansoor Shahid
Research School of Biology, The Australian National University, Canberra, ACT 2601, Australia.
Department of Biological Sciences, University of Sialkot, Sialkot 51040, Pakistan.
Viruses. 2025 Apr 27;17(5):631. doi: 10.3390/v17050631.
Over the last 40 years, several studies have provided evidence demonstrating that viral vectors can result in effective gene targeting/insertions in a host's genome. The traditional approaches of gene knock-down, -out, or -in involve an intensive transgenesis process that is plagued by extensive timescales. Plant viruses have the potential to target specific genes and integrate exogenous DNA molecules at the target locus. Their ability to manipulate a host's genetic material and become a part of it makes them remarkable agents and helpful for molecular and synthetic biology. In this review, we describe how geminivirus-based vectors can be utilized to overcome traditional transgenesis. We highlight the progress that has been made so far and also discuss the hurdles that hinder the employment of geminivirus-based vectors. Furthermore, we conclude with a comparison of geminivirus-based vectors with other plant-derived vectors. Geminivirus-based vectors stand poised to revolutionize plant genome editing by making nucleic acid manipulation cheaper and easier to deploy, thus lessening the major technical constraints, including homology-directed repair (HDR)-mediated genome editing and time-inefficient tissue culture procedures. The insights given in this review illustrate a broader picture of geminiviral vectors, with an emphasis on engineering plant viruses to ease genome editing practices for crop improvements as well as boost experimental timescales from years to months.
在过去的40年里,多项研究提供了证据,证明病毒载体可在宿主基因组中实现有效的基因靶向/插入。传统的基因敲低、敲除或敲入方法涉及一个密集的转基因过程,该过程受到较长时间尺度的困扰。植物病毒有可能靶向特定基因并在目标位点整合外源DNA分子。它们操纵宿主遗传物质并成为其一部分的能力使其成为引人注目的媒介,对分子生物学和合成生物学很有帮助。在这篇综述中,我们描述了基于双生病毒的载体如何被用于克服传统转基因方法。我们强调了迄今为止所取得的进展,并讨论了阻碍基于双生病毒的载体应用的障碍。此外,我们通过将基于双生病毒的载体与其他植物源载体进行比较来得出结论。基于双生病毒的载体有望通过使核酸操作更便宜且更易于应用,从而减少包括同源定向修复(HDR)介导的基因组编辑和耗时低效的组织培养程序等主要技术限制,来彻底改变植物基因组编辑。本综述中的见解展示了双生病毒载体的更广阔图景,重点是改造植物病毒以简化用于作物改良的基因组编辑实践,并将实验时间尺度从数年缩短至数月。