Targeted insertion of large genetic payloads using cas directed LINE-1 reverse transcriptase

被引:3
|
作者
Manoj, Femila [1 ]
Tai, Laura W. [2 ]
Wang, Katelyn Sun Mi [3 ]
Kuhlman, Thomas E. [3 ]
机构
[1] Univ Calif Riverside, Microbiol Program, Riverside, CA 92521 USA
[2] Univ Calif Riverside, Dept Biol, Riverside, CA 92521 USA
[3] Univ Calif Riverside, Dept Phys & Astron, Riverside, CA 92521 USA
关键词
SOCIAL-BEHAVIOR; BREAK REPAIR; RNA; CRISPR-CAS9; RETROTRANSPOSITION; ENDONUCLEASE; MUTAGENESIS; INTEGRATION; GENERATION; EFFICIENCY;
D O I
10.1038/s41598-021-03130-0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
A difficult genome editing goal is the site-specific insertion of large genetic constructs. Here we describe the GENEWRITE system, where site-specific targetable activity of Cas endonucleases is coupled with the reverse transcriptase activity of the ORF2p protein of the human retrotransposon LINE-1. This is accomplished by providing two RNAs: a guide RNA targeting Cas endonuclease activity and an appropriately designed payload RNA encoding the desired insertion. Using E. coli as a simple platform for development and deployment, we show that with proper payload design and co-expression of helper proteins, GENEWRITE can enable insertion of large genetic payloads to precise locations, although with off-target effects, using the described approach. Based upon these results, we describe a potential strategy for implementation of GENEWRITE in more complex systems.
引用
收藏
页数:9
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