A TALEN genome editing system to generate human stem cell-based disease models
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 the use of TALENs to rapidly and efficiently generate mutant alleles of 15 genes in cultured s...
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Veröffentlicht in: | Cell stem cell 2012-12, Vol.12 (2), p.238-251 |
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creator | Ding, Qiurong Lee, Youn-Kyoung Schaefer, Esperance A. K. Peters, Derek T. Veres, Adrian Kim, Kevin Kuperwasser, Nicolas Motola, Daniel L. Meissner, Torsten B. Hendriks, William T. Trevisan, Marta Gupta, Rajat M. Moisan, Annie Banks, Eric Friesen, Max Schinzel, Robert T. Xia, Fang Tang, Alexander Xia, Yulei Figueroa, Emmanuel Wann, Amy Ahfeldt, Tim Daheron, Laurence Zhang, Feng Rubin, Lee L. Peng, Lee F. Chung, Raymond T. Musunuru, Kiran Cowan, Chad A. |
description | 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 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 of 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 find 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. |
doi_str_mv | 10.1016/j.stem.2012.11.011 |
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K. ; Peters, Derek T. ; Veres, Adrian ; Kim, Kevin ; Kuperwasser, Nicolas ; Motola, Daniel L. ; Meissner, Torsten B. ; Hendriks, William T. ; Trevisan, Marta ; Gupta, Rajat M. ; Moisan, Annie ; Banks, Eric ; Friesen, Max ; Schinzel, Robert T. ; Xia, Fang ; Tang, Alexander ; Xia, Yulei ; Figueroa, Emmanuel ; Wann, Amy ; Ahfeldt, Tim ; Daheron, Laurence ; Zhang, Feng ; Rubin, Lee L. ; Peng, Lee F. ; Chung, Raymond T. ; Musunuru, Kiran ; Cowan, Chad A.</creatorcontrib><description>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 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 of 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 find 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.</description><identifier>ISSN: 1934-5909</identifier><identifier>EISSN: 1875-9777</identifier><identifier>DOI: 10.1016/j.stem.2012.11.011</identifier><identifier>PMID: 23246482</identifier><language>eng</language><ispartof>Cell stem cell, 2012-12, Vol.12 (2), p.238-251</ispartof><rights>2012 ll Press. 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title | A TALEN genome editing system to generate human stem cell-based disease models |
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