Parums Dinah V
Science Editor, Medical Science Monitor, International Scientific Information, Inc., Melville, NY, USA.
Med Sci Monit. 2024 Aug 1;30:e945933. doi: 10.12659/MSM.945933.
Therapeutic human gene editing technologies continue to advance, with the endonuclease, clustered regularly interspaced short palindromic repeats (CRISPR) being one of the most rapidly developing technologies. Recently, in 2024, a method of RNA editing called 'bridge editing' has been described in bacteria, which is more powerful and has broader applications than CRISPR to reshape the genome. The term 'bridge editing' is used because the method physically links, or bridges, two sections of DNA and can alter large sections of a genome. 'Bridge editing' relies on insertion sequence (IS) elements, the simplest autonomous transposable elements in prokaryotic genomes. This method provides a unified mechanism for the three fundamental types of DNA rearrangement required for genome design: inversion, insertion, and excision. The 'bridge' recombination system could expand the range and diversity of nucleic acid-guided therapeutic systems beyond RNA interference and CRISPR. This editorial aims to introduce new developments in 'bridge' RNA editing that have the increased potential to reshape the genome.
治疗性人类基因编辑技术不断进步,其中核酸内切酶——成簇规律间隔短回文重复序列(CRISPR)是发展最为迅速的技术之一。最近,在2024年,一种名为“桥接编辑”的RNA编辑方法在细菌中被描述,它比CRISPR更强大,在重塑基因组方面具有更广泛的应用。之所以使用“桥接编辑”这个术语,是因为该方法在物理上连接或桥接了DNA的两个部分,并且可以改变基因组的大片段。“桥接编辑”依赖于插入序列(IS)元件,这是原核基因组中最简单的自主转座元件。该方法为基因组设计所需的三种基本类型的DNA重排(倒位、插入和切除)提供了一种统一机制。“桥接”重组系统可以将核酸引导的治疗系统的范围和多样性扩展到RNA干扰和CRISPR之外。这篇社论旨在介绍“桥接”RNA编辑的新进展,这些进展在重塑基因组方面具有更大的潜力。