Safeguarding CRISPR-Cas9 gene drives in yeast

被引:212
作者
DiCarlo, James E. [1 ,2 ,3 ]
Chavez, Alejandro [1 ,2 ,4 ,5 ]
Dietz, Sven L. [1 ,2 ,4 ,6 ]
Esvelt, Kevin M. [2 ,4 ]
Church, George M. [1 ,2 ,4 ]
机构
[1] Harvard Univ, Sch Med, Dept Genet, Boston, MA USA
[2] Harvard Univ, Sch Med, Boston, MA 02115 USA
[3] Boston Univ, Dept Biomed Engn, Boston, MA 02215 USA
[4] Wyss Inst Biol Inspired Engn, Boston, MA USA
[5] Massachusetts Gen Hosp, Dept Pathol, Boston, MA 02114 USA
[6] Swiss Fed Inst Technol, Dept Biosyst Sci & Engn, Basel, Switzerland
基金
美国国家科学基金会;
关键词
DROSOPHILA; SYSTEM; CAS9; DNA; GENERATION; MUTATIONS; GERMLINE; REPAIR; TOOLS;
D O I
10.1038/nbt.3412
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
RNA-guided gene drives capable of spreading genomic alterations made in laboratory organisms through wild populations could be used to address environmental and public health problems. However, the possibility of unintended genome editing occurring through the escape of strains from laboratories, coupled with the prospect of unanticipated ecological change, demands caution. We report the efficacy of CRISPR-Cas9 gene drive systems in wild and laboratory strains of the yeast Saccharomyces cerevisiae. Furthermore, we address concerns surrounding accidental genome editing by developing and validating methods of molecular confinement that minimize the risk of unwanted genome editing. We also present a drive system capable of overwriting the changes introduced by an earlier gene drive. These molecular safeguards should enable the development of safe CRISPR gene drives for diverse organisms.
引用
收藏
页码:1250 / +
页数:8
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