Bloh Kevin, Rivera-Torres Natalia
Gene Editing Institute, Helen F. Graham Cancer Center & Research Institute, ChristianaCare, 4701 Ogletown-Stanton Road, Newark, DE 19710, USA.
Department of Medical and Molecular Sciences, University of Delaware, Newark, DE 19710, USA.
Int J Mol Sci. 2021 Apr 7;22(8):3834. doi: 10.3390/ijms22083834.
The mechanism of action of ssODN-directed gene editing has been a topic of discussion within the field of CRISPR gene editing since its inception. Multiple comparable, but distinct, pathways have been discovered for DNA repair both with and without a repair template oligonucleotide. We have previously described the ExACT pathway for oligo-driven DNA repair, which consisted of a two-step DNA synthesis-driven repair catalyzed by the simultaneous binding of the repair oligonucleotide (ssODN) upstream and downstream of the double-strand break. In order to better elucidate the mechanism of ExACT-based repair, we have challenged the assumptions of the pathway with those outlines in other similar non-ssODN-based DNA repair mechanisms. This more comprehensive iteration of the ExACT pathway better described the many different ways where DNA repair can occur in the presence of a repair oligonucleotide after CRISPR cleavage, as well as how these previously distinct pathways can overlap and lead to even more unique repair outcomes.
自CRISPR基因编辑诞生以来,单链寡脱氧核苷酸(ssODN)导向的基因编辑作用机制一直是该领域讨论的话题。对于有或没有修复模板寡核苷酸的DNA修复,已经发现了多种类似但不同的途径。我们之前描述了寡核苷酸驱动的DNA修复的ExACT途径,该途径由两步DNA合成驱动的修复组成,通过修复寡核苷酸(ssODN)在双链断裂的上游和下游同时结合来催化。为了更好地阐明基于ExACT的修复机制,我们用其他类似的非基于ssODN的DNA修复机制中概述的假设对该途径的假设提出了质疑。ExACT途径的这种更全面的迭代更好地描述了CRISPR切割后在存在修复寡核苷酸的情况下DNA修复可以发生的许多不同方式,以及这些以前不同的途径如何重叠并导致更独特的修复结果。