CRISPR Guide RNA Validation In Vitro.

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

Zebrafish

journal_title

Zebrafish

authors

Grainger S,Lonquich B,Oon CH,Nguyen N,Willert K,Traver D

doi

10.1089/zeb.2016.1358

subject

Has Abstract

pub_date

2017-08-01 00:00:00

pages

383-386

issue

4

eissn

1545-8547

issn

1557-8542

journal_volume

14

pub_type

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