A TALEN Genome-Editing System for Generating Human Stem Cell-Based Disease Models

被引:360
作者
Ding, Qiurong [1 ]
Lee, Youn-Kyoung [1 ]
Schaefer, Esperance A. K. [3 ,5 ]
Peters, Derek T. [1 ,5 ]
Veres, Adrian [1 ,5 ]
Kim, Kevin [1 ]
Kuperwasser, Nicolas [1 ,6 ]
Motola, Daniel L. [3 ,5 ]
Meissner, Torsten B. [1 ]
Hendriks, William T. [1 ,2 ]
Trevisan, Marta [1 ,2 ]
Gupta, Rajat M. [1 ,5 ,6 ]
Moisan, Annie [7 ]
Banks, Eric [8 ]
Friesen, Max [1 ]
Schinzel, Robert T. [1 ]
Xia, Fang [1 ]
Tang, Alexander [1 ]
Xia, Yulei [1 ]
Figueroa, Emmanuel [1 ]
Wann, Amy [1 ]
Ahfeldt, Tim [1 ]
Daheron, Laurence [1 ,2 ]
Zhang, Feng [8 ,9 ]
Rubin, Lee L. [1 ,2 ,3 ]
Peng, Lee F. [3 ,5 ]
Chung, Raymond T. [5 ]
Musunuru, Kiran [1 ,2 ,5 ,6 ,8 ]
Cowan, Chad A. [1 ,2 ,4 ,5 ,8 ]
机构
[1] Harvard Univ, Dept Stem Cell & Regenerat Biol, Cambridge, MA 02138 USA
[2] Harvard Univ, Harvard Stem Cell Inst, Cambridge, MA 02138 USA
[3] Massachusetts Gen Hosp, Dept Med, Gastrointestinal Unit, Boston, MA 02114 USA
[4] Massachusetts Gen Hosp, Ctr Regenerat Med, Boston, MA 02114 USA
[5] Harvard Univ, Sch Med, Dept Med, Boston, MA 02115 USA
[6] Brigham & Womens Hosp, Div Cardiovasc Med, Boston, MA 02115 USA
[7] Roche Pharmaceut, Metab Discovery & Translat Area, CH-4070 Basel, Switzerland
[8] Broad Inst, Cambridge, MA 02142 USA
[9] MIT, McGovern Inst Brain Res, Dept Brain & Cognit Sci, Cambridge, MA 02139 USA
基金
美国国家卫生研究院;
关键词
INSULIN-RESISTANCE; ADIPOSE-TISSUE; MICE LACKING; DNA; EFFECTORS; PERILIPIN; NUCLEASES; SORTILIN; MUTATION; AKT2;
D O I
10.1016/j.stem.2012.11.011
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Transcription activator-like effector nucleases (TALENs) are a new class of engineered nucleases that are easier to design to cleave at desired sites in a genome than previous types of nucleases. We report here the use of TALENs to rapidly and efficiently generate mutant alleles of 15 genes in cultured somatic cells or human pluripotent stem cells, the latter for which we differentiated both the targeted lines and isogenic control lines into various metabolic cell types. We demonstrate cell-autonomous phenotypes directly linked to disease-dyslipidemia, insulin resistance, hypoglycemia, lipodystrophy, motor-neuron death, and hepatitis C infection. We found little evidence of TALEN off-target effects, but each clonal line nevertheless harbors a significant number of unique mutations. Given the speed and ease with which we were able to derive and characterize these cell lines, we anticipate TALEN-mediated genome editing of human cells becoming a mainstay for the investigation of human biology and disease.
引用
收藏
页码:238 / 251
页数:14
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