Wu Wen Y, Adiego-Pérez Belén, van der Oost John
Laboratory of Microbiology, Wageningen University & Research, Wageningen, the Netherlands.
Department of Chemical and Pharmaceutical Biology, Groningen Research Institute of Pharmacy, University of Groningen, Groningen, the Netherlands.
Nat Biotechnol. 2024 Dec;42(12):1807-1821. doi: 10.1038/s41587-024-02485-9. Epub 2024 Dec 4.
CRISPR-associated Cas12 proteins are a highly variable collection of nucleic acid-targeting proteins. All Cas12 variants use RNA guides and a single nuclease domain to target complementary DNA or, in rare cases, RNA. The high variability of Cas12 effectors can be explained by a series of independent evolution events from different transposon-associated TnpB-like ancestors. Despite basic structural and functional similarities, this has resulted in unprecedented variation of the Cas12 effector proteins in terms of size, domain composition, guide structure, target identity and interference strategy. In this Review, we compare the unique molecular features of natural and engineered Cas12 and TnpB variants. Furthermore, we provide an overview of established genome editing and diagnostic applications and discuss potential future directions.
与CRISPR相关的Cas12蛋白是一类高度可变的核酸靶向蛋白。所有Cas12变体都利用RNA向导和单个核酸酶结构域来靶向互补DNA,在极少数情况下也可靶向RNA。Cas12效应蛋白的高度可变性可以通过一系列来自不同转座子相关TnpB样祖先的独立进化事件来解释。尽管在基本结构和功能上存在相似性,但这导致Cas12效应蛋白在大小、结构域组成、向导结构、靶标特性和干扰策略方面出现了前所未有的变异。在本综述中,我们比较了天然和工程化Cas12及TnpB变体的独特分子特征。此外,我们概述了已确立的基因组编辑和诊断应用,并讨论了潜在的未来发展方向。