| Literature DB >> 28581493 |
Cem Kuscu1, Mahmut Parlak1, Turan Tufan1, Jiekun Yang1, Karol Szlachta1, Xiaolong Wei1, Rashad Mammadov1, Mazhar Adli1.
Abstract
CRISPR-Cas9-induced DNA damage may have deleterious effects at high-copy-number genomic regions. Here, we use CRISPR base editors to knock out genes by changing single nucleotides to create stop codons. We show that the CRISPR-STOP method is an efficient and less deleterious alternative to wild-type Cas9 for gene-knockout studies. Early stop codons can be introduced in ∼17,000 human genes. CRISPR-STOP-mediated targeted screening demonstrates comparable efficiency to WT Cas9, which indicates the suitability of our approach for genome-wide functional screenings.Entities:
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Year: 2017 PMID: 28581493 DOI: 10.1038/nmeth.4327
Source DB: PubMed Journal: Nat Methods ISSN: 1548-7091 Impact factor: 28.547