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
Hauptverfasser: 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.
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container_issue 2
container_start_page 238
container_title Cell stem cell
container_volume 12
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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title A TALEN genome editing system to generate human stem cell-based disease models
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