In vivo Genome Editing Using High Efficiency TALENs
The zebrafish ( Danio rerio ) is increasingly being used to study basic vertebrate biology and human disease using a rich array of in vivo genetic and molecular tools. However, the inability to readily modify the genome in a targeted fashion has been a bottleneck in the field. Here we show that impr...
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Published in: | Nature (London) Vol. 491; no. 7422; pp. 114 - 118 |
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Main Authors: | , , , , , , , , , , , , , , , |
Format: | Journal Article |
Language: | English |
Published: |
23-09-2012
|
Online Access: | Get full text |
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Summary: | The zebrafish (
Danio rerio
) is increasingly being used to study basic vertebrate biology and human disease using a rich array of
in vivo
genetic and molecular tools. However, the inability to readily modify the genome in a targeted fashion has been a bottleneck in the field. Here we show that improvements in artificial transcription activator-like effector nucleases (TALENs) provide a powerful new approach for targeted zebrafish genome editing and functional genomic applications
1
–
5
. Using the GoldyTALEN modified scaffold and zebrafish delivery system, we show this enhanced TALEN toolkit demonstrates a high efficiency in inducing locus-specific DNA breaks in somatic and germline tissues. At some loci, this efficacy approaches 100%, including biallelic conversion in somatic tissues that mimics phenotypes seen using morpholino (MO)-based targeted gene knockdowns
6
. With this updated TALEN system, we successfully used single-stranded DNA (ssDNA) oligonucleotides (oligos) to precisely modify sequences at predefined locations in the zebrafish genome through homology-directed repair (HDR), including the introduction of a custom-designed
EcoRV
site and a modified loxP (mloxP) sequence into somatic tissue
in vivo
. We further show successful germline transmission of both
EcoRV
and mloxP engineered chromosomes. This combined approach offers the potential to model genetic variation as well as to generate targeted conditional alleles. |
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Bibliography: | These authors contributed equally to this work. |
ISSN: | 0028-0836 1476-4687 |
DOI: | 10.1038/nature11537 |