PUBLICATION
TALEN construction via "Unit Assembly" method and targeted genome modifications in zebrafish
- Authors
- Huang, P., Xiao, A., Tong, X., Zu, Y., Wang, Z., Zhang, B.
- ID
- ZDB-PUB-140513-497
- Date
- 2014
- Source
- Methods (San Diego, Calif.) 69(1): 67-75 (Journal)
- Registered Authors
- Tong, Xiangjun, Wang, Zhanxiang, Xiao, An, Zhang, Bo, Zu, Yao
- Keywords
- Chromosomal deletion, Gene targeting, Genome manipulation, Homologous recombination, TALEN, Zebrafish
- MeSH Terms
-
- Animals
- Chromosome Deletion
- Deoxyribonucleases/chemistry*
- Deoxyribonucleases/genetics
- Gene Knock-In Techniques
- Gene Knockout Techniques
- Genetic Engineering/methods*
- Germ-Line Mutation
- Homologous Recombination
- Protein Engineering/methods
- Zebrafish/genetics
- PubMed
- 24556555 Full text @ Methods
Citation
Huang, P., Xiao, A., Tong, X., Zu, Y., Wang, Z., Zhang, B. (2014) TALEN construction via "Unit Assembly" method and targeted genome modifications in zebrafish. Methods (San Diego, Calif.). 69(1):67-75.
Abstract
Transcription activator-like effector nucleases (TALENs) are engineered endonucleases composed of a customized transcription activator-like effector (TALE) DNA-binding domain and a FokI DNA cleavage domain. TALENs induce DNA double-strand breaks (DSBs) at their target sites on the chromosome and have been successfully used for genome engineering in many species and cultured cells. Zebrafish is a very popular model organism in both basic and clinical research. Here, we describe the details of construction of customized TALENs using the "Unit Assembly" (UA) method, as well as three applications of zebrafish genome manipulations using TALENs: gene knock-out, large chromosome deletion, and gene knock-in by homologous recombination.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping