Epigenetics Institute, Department of Cell and Developmental Biology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, USA.
Cell Rep Methods. 2023 Aug 22;3(8):100564. doi: 10.1016/j.crmeth.2023.100564. eCollection 2023 Aug 28.
Golden Gate Assembly is an efficient and rapid cloning method but requires dedicated vectors. Here, we modified Golden Gate to expand its compatibility to a broader range of destination vectors while maintaining its strengths. Our Expanded Golden Gate (ExGG) assembly adds to the insert(s) type IIS restriction sites that generate protruding ends compatible with traditional type IIP sites on the recipient vector. The ligated product cannot be cleaved again, owing to a single-base change near the junction. This allows the reaction to proceed in a single tube without an intermediate purification step. ExGG can be used to introduce multiple fragments into a vector simultaneously, including shorter fragments (<100 bp) and fragments with shared sequences, which can be difficult to assemble with other fast cloning strategies. Thus, ExGG extends the convenience of Golden Gate to a much larger space of pre-existing vectors designed for conventional cloning.
金门组装是一种高效快速的克隆方法,但需要专用载体。在这里,我们对金门进行了修改,使其在保持原有优势的基础上,能够与更广泛的目标载体兼容。我们的扩展金门(ExGG)组装在插入物(s)上添加了 II 型限制酶识别位点,这些位点产生与受体载体上传统的 IIP 位点兼容的突出末端。由于连接点附近的单个碱基变化,连接产物不能再次被切割。这使得反应可以在单个管中进行,而无需中间纯化步骤。ExGG 可以同时将多个片段引入载体中,包括较短的片段(<100 bp)和具有共享序列的片段,这些片段用其他快速克隆策略很难组装。因此,ExGG 将金门的便利性扩展到了为传统克隆设计的更大范围的现有载体空间。