Genomic editing opens new avenues for zebrafish as a model for neurodegeneration
J Neurochem. 2013 Oct 9. doi: 10.1111/jnc.12460. [Epub ahead of print]
| Authors/Editors: | Schmid B, Haass C. |
|---|---|
| Publication Date: | 2013 |
Abstract
Zebrafish has become a popular model organism to study human diseases. We will highlight the advantages and limitations of zebrafish as a model organism to study neurodegenerative diseases and introduce zinc finger nucleases, transcription activator-like effector nucleases, and the recently established clustered regularly interspaced short palindromic repeats/clustered regularly interspaced short palindromic repeat-associated system for genome editing. The efficiency of the novel genome editing tools now greatly facilitates knock-out and, importantly, also makes knock-in approaches feasible in zebrafish. Genome editing in zebrafish avoids unspecific phenotypes caused by off-target effects and toxicity as frequently seen in conventional knock-down approaches.
