当前位置:科学网首页 > 小柯机器人 >详情
科学家开发出超快CRISPR技术
作者:小柯机器人 发布时间:2020/6/14 14:09:30

美国约翰霍普金斯大学Taekjip Ha、Bin Wu等研究人员合作开发出超快CRISPR技术。该项研究成果发表在2020年6月12日出版的《科学》杂志上。

研究人员开发了一种笼状的RNA策略,该策略能够让Cas9结合DNA,但在光诱导的激活作用下才能剪切。这种方法被称为超快CRISPR(vfCRISPR),可在亚微米和秒级产生双链断裂(DSB)。同步切割改善了对DNA修复的动力学分析,揭示了细胞在几分钟内对Cas9诱导的DSB作出反应,并且在DNA连接后可以保留MRE11。DNA损伤后H2AX的磷酸化每分钟传播100多个碱基,达到30兆碱基。
 
使用单细胞荧光成像,研究人员表征了53BP1修复灶形成和溶解的多个周期,第一个周期比随后的周期更长,并且其持续时间受修复抑制作用的调节。成像引导的亚细胞Cas9激活进一步促进了单等位基因分辨率的基因组操作。vfCRISPR可以在空间、时间和基因组坐标上进行高分辨率的DNA修复研究。
 
据悉,CRISPR-Cas系统提供了用于可编程基因组编辑的多功能工具。
 
附:英文原文

Title: Very fast CRISPR on demand

Author: Yang Liu, Roger S. Zou, Shuaixin He, Yuta Nihongaki, Xiaoguang Li, Shiva Razavi, Bin Wu, Taekjip Ha

Issue&Volume: 2020/06/12

Abstract: CRISPR-Cas systems provide versatile tools for programmable genome editing. Here, we developed a caged RNA strategy that allows Cas9 to bind DNA but not cleave until light-induced activation. This approach, referred to as very fast CRISPR (vfCRISPR), creates double-strand breaks (DSBs) at the submicrometer and second scales. Synchronized cleavage improved kinetic analysis of DNA repair, revealing that cells respond to Cas9-induced DSBs within minutes and can retain MRE11 after DNA ligation. Phosphorylation of H2AX after DNA damage propagated more than 100 kilobases per minute, reaching up to 30 megabases. Using single-cell fluorescence imaging, we characterized multiple cycles of 53BP1 repair foci formation and dissolution, with the first cycle taking longer than subsequent cycles and its duration modulated by inhibition of repair. Imaging-guided subcellular Cas9 activation further facilitated genomic manipulation with single-allele resolution. vfCRISPR enables DNA-repair studies at high resolution in space, time, and genomic coordinates.

DOI: 10.1126/science.aay8204

Source: https://science.sciencemag.org/content/368/6496/1265

期刊信息
Science:《科学》,创刊于1880年。隶属于美国科学促进会,最新IF:41.037