Mutagenesis and phenotyping resources in zebrafish for studying development and human disease
Author(s) -
Gaurav K. Varshney,
Shawn M. Burgess
Publication year - 2013
Publication title -
briefings in functional genomics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.22
H-Index - 67
eISSN - 2041-2647
pISSN - 2041-2649
DOI - 10.1093/bfgp/elt042
Subject(s) - zebrafish , biology , crispr , transcription activator like effector nuclease , zinc finger nuclease , gene knockout , mutagenesis , forward genetics , genome editing , genetics , model organism , reverse genetics , computational biology , genetic screen , gene targeting , cas9 , gene , effector , genome , phenotype , mutant , microbiology and biotechnology
The zebrafish (Danio rerio) is an important model organism for studying development and human disease. The zebrafish has an excellent reference genome and the functions of hundreds of genes have been tested using both forward and reverse genetic approaches. Recent years have seen an increasing number of large-scale mutagenesis projects and the number of mutants or gene knockouts in zebrafish has increased rapidly, including for the first time conditional knockout technologies. In addition, targeted mutagenesis techniques such as zinc finger nucleases, transcription activator-like effector nucleases and clustered regularly interspaced short sequences (CRISPR) or CRISPR-associated (Cas), have all been shown to effectively target zebrafish genes as well as the first reported germline homologous recombination, further expanding the utility and power of zebrafish genetics. Given this explosion of mutagenesis resources, it is now possible to perform systematic, high-throughput phenotype analysis of all zebrafish gene knockouts.
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