Transposons and CRISPR: Rewiring Gene Editing

IF 2.9 3区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Biochemistry Biochemistry Pub Date : 2022-09-21 DOI:10.1021/acs.biochem.2c00379
Francisco Tenjo-Castaño, Guillermo Montoya* and Arturo Carabias, 
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引用次数: 2

Abstract

CRISPR-Cas is driving a gene editing revolution because of its simple reprogramming. However, off-target effects and dependence on the double-strand break repair pathways impose important limitations. Because homology-directed repair acts primarily in actively dividing cells, many of the current gene correction/replacement approaches are restricted to a minority of cell types. Furthermore, current approaches display low efficiency upon insertion of large DNA cargos (e.g., sequences containing multiple gene circuits with tunable functionalities). Recent research has revealed new links between CRISPR-Cas systems and transposons providing new scaffolds that might overcome some of these limitations. Here, we comment on two new transposon-associated RNA-guided mechanisms considering their potential as new gene editing solutions. Initially, we focus on a group of small RNA-guided endonucleases of the IS200/IS605 family of transposons, which likely evolved into class 2 CRISPR effector nucleases (Cas9s and Cas12s). We explore the diversity of these nucleases (named OMEGA, obligate mobile element-guided activity) and analyze their similarities with class 2 gene editors. OMEGA nucleases can perform gene editing in human cells and constitute promising candidates for the design of new compact RNA-guided platforms. Then, we address the co-option of the RNA-guided activity of different CRISPR effector nucleases by a specialized group of Tn7-like transposons to target transposon integration. We describe the various mechanisms used by these RNA-guided transposons for target site selection and integration. Finally, we assess the potential of these new systems to circumvent some of the current gene editing challenges.

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转座子和CRISPR:重组基因编辑。
CRISPR-Cas由于其简单的重编程,正在推动一场基因编辑革命。然而,脱靶效应和对双链断裂修复途径的依赖性造成了重要的局限性。由于同源性定向修复主要在活跃分裂的细胞中起作用,因此目前的许多基因校正/替换方法仅限于少数细胞类型。此外,当前的方法在插入大的DNA货物(例如,包含具有可调功能的多个基因回路的序列)时显示出低效率。最近的研究揭示了CRISPR-Cas系统和转座子之间的新联系,提供了可能克服其中一些限制的新支架。在这里,我们评论了两种新的转座子相关RNA引导机制,考虑到它们作为新的基因编辑解决方案的潜力。最初,我们关注的是转座子IS200/IS605家族的一组小RNA引导的核酸内切酶,它们可能进化为2类CRISPR效应核酸酶(Cas9s和Cas12s)。我们探索了这些核酸酶(命名为OMEGA,专性移动元件引导活性)的多样性,并分析了它们与2类基因编辑器的相似性。OMEGA核酸酶可以在人类细胞中进行基因编辑,并构成设计新型紧凑型RNA引导平台的有希望的候选者。然后,我们讨论了通过一组专门的Tn7样转座子来靶向转座子整合,RNA引导不同CRISPR效应核酸酶活性的共同选择。我们描述了这些RNA引导的转座子用于靶位点选择和整合的各种机制。最后,我们评估了这些新系统规避当前基因编辑挑战的潜力。
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来源期刊
Biochemistry Biochemistry
Biochemistry Biochemistry 生物-生化与分子生物学
CiteScore
5.50
自引率
3.40%
发文量
336
审稿时长
1-2 weeks
期刊介绍: Biochemistry provides an international forum for publishing exceptional, rigorous, high-impact research across all of biological chemistry. This broad scope includes studies on the chemical, physical, mechanistic, and/or structural basis of biological or cell function, and encompasses the fields of chemical biology, synthetic biology, disease biology, cell biology, nucleic acid biology, neuroscience, structural biology, and biophysics. In addition to traditional Research Articles, Biochemistry also publishes Communications, Viewpoints, and Perspectives, as well as From the Bench articles that report new methods of particular interest to the biological chemistry community.
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