转座因子
清脆的
基因组
核糖核酸
流动遗传元素
计算生物学
生物
使负有责任或义务
基因组工程
合成生物学
遗传学
基因
基因组编辑
生态学
作者
Chin-Wei Chang,Vy Anh Truong,Nam Ngoc Pham,Yu‐Chen Hu
标识
DOI:10.1016/j.tibtech.2024.02.006
摘要
CRISPR-Cas systems revolutionized the genome engineering field but need to induce double-strand breaks (DSBs) and may be difficult to deliver due to their large protein size. Tn7-like transposons such as CRISPR-associated transposons (CASTs) can be repurposed for RNA-guided DSB-free integration, and obligate mobile element guided activity (OMEGA) proteins of the IS200/IS605 transposon family have been developed as hypercompact RNA-guided genome editing tools. CASTs and OMEGA are exciting, innovative genome engineering tools that can improve the precision and efficiency of editing. This review explores the recent developments and uses of CASTs and OMEGA in genome editing across prokaryotic and eukaryotic cells. The pros and cons of these transposon-based systems are deliberated in comparison to other CRISPR systems.
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