Abstract:
:Clustered regularly interspaced short palindromic repeats (CRISPR)/Cas9 has been applied to edit genomes in a wide variety of model systems. Although this process can be quite efficient, editing at precise locations in the genome remains difficult without a suitable single guide RNA (sgRNA). We have developed a method for screening sgRNA function in vitro, using reagents that most zebrafish laboratories are already using. The results from our in vitro assay correlate with function in vivo in every sgRNA that we have examined so far. When combined with endonucleases with alternative protospacer adjacent motif site specificities and alternative sgRNAs, this method will streamline genome editing at almost any locus.
journal_name
Zebrafishjournal_title
Zebrafishauthors
Grainger S,Lonquich B,Oon CH,Nguyen N,Willert K,Traver Ddoi
10.1089/zeb.2016.1358subject
Has Abstractpub_date
2017-08-01 00:00:00pages
383-386issue
4eissn
1545-8547issn
1557-8542journal_volume
14pub_type
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