Advances in genetic modification technologies.
- Author:
Baixue ZHANG
;
Qixin SUN
;
Haifeng LI
- Publication Type:Journal Article
- MeSH:
Animals;
CRISPR-Cas Systems;
DNA Breaks, Double-Stranded;
Endonucleases;
Genetic Engineering;
methods;
Humans;
Mutagenesis, Insertional;
Mutagenesis, Site-Directed;
Plants;
Zinc Fingers
- From:
Chinese Journal of Biotechnology
2015;31(8):1162-1174
- CountryChina
- Language:Chinese
-
Abstract:
Genetic modification technology is a new molecular tool for targeted genome modification. It includes zinc finger nucleases (ZFN) technology, transcription activator-like effector nucleases (TALEN) technology and clustered regularly interspaced short palindromic repeat (CRISPR)-associated (Cas) (CRISPR-Cas) nucleases technology. All of these nucleases create DNA double-strand breaks (DSB) at chromosomal targeted sites and induce cell endogenous mechanisms that are primarily repaired by the non-homologous end joining (NHEJ) or homologous recombination (HR) pathway, resulting in targeted endogenous gene knock-out or exogenous gene insertion. In recent years, genetic modification technologies have been successfully applied to bacteria, yeast, human cells, fruit fly, zebra fish, mouse, rat, livestock, cynomolgus monkey, Arabidopsis, rice, tobacco, maize, sorghum, wheat, barley and other organisms, showing its enormous advantage in gene editing field. Especially, the newly developed CRISPR-Cas9 system arose more attention because of its low cost, high effectiveness, simplicity and easiness. We reviewed the principles and the latest research progress of these three technologies, as well as prospect of future research and applications.
