CRISPR-Cas9 System as a Versatile Tool for Genome Engineering in Human Cells
Author(s) -
Xuelian Wang,
Xiumin Huang,
Xiuli Fang,
Youzhong Zhang,
Wanpeng Wang
Publication year - 2016
Publication title -
molecular therapy — nucleic acids
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.208
H-Index - 59
ISSN - 2162-2531
DOI - 10.1038/mtna.2016.95
Subject(s) - crispr , genome engineering , cas9 , genome editing , computational biology , human genome , genome , computer science , biology , software engineering , engineering , genetics , gene
Targeted nucleases are influential instruments for intervening in genome revision with great accuracy. RNA-guided Cas9 nucleases produced from clustered regularly interspaced short palindromic repeats (CRISPR)-Cas systems have noticeably altered the means to modify the genomes of distinct organisms. They can be notably used to facilitate effective genome manipulation in eukaryotic cells by clearly detailing a 20-nt targeting sequence inside its directed RNA. We discuss the most recent advancements in the molecular basis of the type II CRISPR/Cas system and encapsulate applications and elements affecting its use in human cells. We also propose possible applications covering its uses ranging from basic science to implementation in the clinic
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