Department of Systems Biotechnology, Chung-Ang University, Anseong 17546, Republic of Korea.
J Microbiol Biotechnol. 2020 Sep 28;30(9):1273-1281. doi: 10.4014/jmb.2003.03046.
Due to the broad host suitability of viral vectors and their high gene delivery capacity, many researchers are focusing on viral vector-mediated gene therapy. Among the retroviruses, foamy viruses have been considered potential gene therapy vectors because of their non-pathogenicity. To date, the prototype foamy virus is the only retrovirus that has a high-resolution structure of intasomes, nucleoprotein complexes formed by integrase, and viral DNA. The integration of viral DNA into the host chromosome is an essential step for viral vector development. This process is mediated by virally encoded integrase, which catalyzes unique chemical reactions. Additionally, recent studies on foamy virus integrase elucidated the catalytic functions of its three distinct domains and their effect on viral pathogenicity. This review focuses on recent advancements in biochemical, structural, and functional studies of foamy virus integrase for gene therapy vector research.
由于病毒载体宿主适应性广泛,基因转导容量高,许多研究人员都专注于病毒载体介导的基因治疗。在逆转录病毒中,泡沫病毒因其非致病性而被认为是有潜力的基因治疗载体。迄今为止,原代泡沫病毒是唯一一种整合酶内合体复合物(由整合酶形成的核蛋白复合物)和病毒 DNA 具有高分辨率结构的逆转录病毒。病毒 DNA 整合到宿主染色体是病毒载体开发的关键步骤。该过程由病毒编码的整合酶介导,其催化独特的化学反应。此外,最近对泡沫病毒整合酶的研究阐明了其三个不同结构域的催化功能及其对病毒致病性的影响。本综述重点介绍了泡沫病毒整合酶在基因治疗载体研究方面的生化、结构和功能研究的最新进展。