Division of Laboratory Animal Research, Aichi Medical University School of Medicine, Nagakute, Aichi 480-1195, Japan.
Department of Molecular Genetics, Institute of Biomedical Sciences, Fukushima Medical University School of Medicine, Fukushima 960-1295, Japan.
Cell Rep Methods. 2023 Jan 18;3(2):100393. doi: 10.1016/j.crmeth.2022.100393. eCollection 2023 Feb 27.
The flip-excision switch (FLEX) system with an adeno-associated viral (AAV) vector allows expression of transgenes in specific cell populations having Cre recombinase. A significant issue with this system is non-specific expression of transgenes in tissues after vector injection. We show here that Cre-independent recombination events in the AAV genome carrying the FLEX sequence occur mainly during the production of viral vectors in packaging cells, which results in transgene expression in off-target populations. Introduction of a relatively longer nucleotide sequence between two recognition sites at the unilateral side of the transgene cassette, termed a unilateral spacer sequence (USS), is useful to suppress the recombination in the viral genome, leading to the protection of non-specific transgene expression with enhanced gene expression selectivity. Our FLEX/USS system offers a powerful strategy for highly specific Cre-dependent transgene expression, aiming at various applications for structural and functional analyses of target cell populations.
翻转切除开关 (FLEX) 系统与腺相关病毒 (AAV) 载体结合使用,可以在具有 Cre 重组酶的特定细胞群中表达转基因。该系统的一个重要问题是载体注射后转基因在组织中的非特异性表达。我们在这里表明,携带 FLEX 序列的 AAV 基因组中的 Cre 非依赖性重组事件主要发生在包装细胞生产病毒载体期间,这导致转基因在非靶细胞群体中的表达。在转基因盒单侧的两个识别位点之间引入相对较长的核苷酸序列,称为单侧间隔序列 (USS),可有效抑制病毒基因组中的重组,从而保护非特异性转基因表达,并提高基因表达的选择性。我们的 FLEX/USS 系统为高度特异性 Cre 依赖性转基因表达提供了一种强大的策略,旨在针对靶细胞群体的结构和功能分析的各种应用。