Rescue of high-specificity Cas9 variants using sgRNAs with matched 5’ nucleotides
Abstract We report that engineered Cas9 variants with improved specificity—eCas9-1.1 and Cas9-HF1—are often poorly active in human cells, when complexed with single guide RNAs (sgRNAs) with a mismatch at the 5’ terminus, relative to target DNA sequences. Because the nucleotide at the 5’ end of sgRNA...
Main Authors: | Sojung Kim, Taegeun Bae, Jaewoong Hwang, Jin-Soo Kim |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2017-11-01
|
Series: | Genome Biology |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s13059-017-1355-3 |
Similar Items
-
CRISPy-web: An online resource to design sgRNAs for CRISPR applications
by: Kai Blin, et al.
Published: (2016-06-01) -
Development and design of CRISPR-based diagnostic for Acinetobacter baumannii by employing off-target gene editing of sgRNA
by: Zulqarnain Baqar, et al.
Published: (2024-01-01) -
Mismatch Intolerance of 5′-Truncated sgRNAs in CRISPR/Cas9 Enables Efficient Microbial Single-Base Genome Editing
by: Ho Joung Lee, et al.
Published: (2021-06-01) -
Effects of sgRNA length and number on gene editing efficiency and predicted mutations generated in rice
by: Xiaojing Liu, et al.
Published: (2022-04-01) -
CRISPR/Cas Systems in Genome Editing: Methodologies and Tools for sgRNA Design, Off‐Target Evaluation, and Strategies to Mitigate Off‐Target Effects
by: Hakim Manghwar, et al.
Published: (2020-03-01)