School of Biomedical and Pharmaceutical Sciences, Guangdong University of Technology, Guangzhou, China.
CAS Key Laboratory of Regenerative Biology, Guangzhou Institutes of Biomedicine and Health, Chinese Academy of Sciences, Guangzhou, China.
PLoS One. 2023 Aug 4;18(8):e0289509. doi: 10.1371/journal.pone.0289509. eCollection 2023.
Transcription activator-like effectors (TALEs) have been widely used for genome editing, transcriptional regulation, and locus-specific DNA imaging. However, TALEs are difficult to handle in routine laboratories because of their complexity and the considerable time consumed in TALE construction. Here, we described a simple and rapid TALE assembly method based on uracil-specific excision reagent (USER) cloning. Polymerase chain reaction was amplified with TALE trimer templates and deoxyuridine-containing primers. The products were treated with USER at 37°C for 30 min, followed by the treatment of T4 DNA Ligase at 16°C for 30 min. The TALE trimer unit could be rejoined hierarchically to form complete TALE expression vectors with high efficiency. This method was adopted to construct TALE-deaminases, which were used in combination with Cas9 nickases to generate efficient C-to-T or A-to-G base editing while eliminating predictable DNA off-target effects. This improved USER assembly is a simple, rapid, and laboratory-friendly TALE construction technique that will be valuable for DNA targeting.
转录激活样效应因子(TALEs)已被广泛应用于基因组编辑、转录调控和特定基因座的 DNA 成像。然而,由于 TALEs 结构复杂,构建 TALEs 耗费时间长,在常规实验室中难以处理。在这里,我们描述了一种基于尿嘧啶特异性切除试剂(USER)克隆的简单、快速的 TALE 组装方法。利用 TALE 三聚体模板和含脱氧尿嘧啶的引物进行聚合酶链反应扩增。将产物在 37°C 下用 USER 处理 30 分钟,然后在 16°C 下用 T4 DNA 连接酶处理 30 分钟。TALE 三聚体单元可以分层重新连接,高效地形成完整的 TALE 表达载体。该方法被用于构建 TALE 脱氨酶,这些脱氨酶与 Cas9 切口酶结合使用,在消除可预测的 DNA 脱靶效应的同时,有效地将 C 碱基转换为 T 碱基或 A 碱基转换为 G 碱基。这种改进的 USER 组装方法是一种简单、快速且对实验室友好的 TALE 构建技术,将对 DNA 靶向具有重要价值。