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Gene editing of human embryonic stem cells via an engineered baculoviral vector carrying zinc-finger nucleases.


ABSTRACT: Human embryonic stem (hES) cells are renewable cell sources that have potential applications in regenerative medicine. The development of technologies to produce permanent and site-specific genome modifications is in demand to achieve future medical implementation of hES cells. We report herein that a baculoviral vector (BV) system carrying zinc-finger nucleases (ZFNs) can successfully modify the hES cell genome. BV-mediated transient expression of ZFNs specifically disrupted the CCR5 locus in transduced cells and the modified cells exhibited resistance to HIV-1 transduction. To convert the BV to a gene targeting vector, a DNA donor template and ZFNs were incorporated into the vector. These hybrid vectors yielded permanent site-specific gene addition in both immortalized human cell lines (10%) and hES cells (5%). Modified hES cells were both karyotypically normal and pluripotent. These results suggest that this baculoviral delivery system can be engineered for site-specific genetic manipulation in hES cells.

SUBMITTER: Lei Y 

PROVIDER: S-EPMC3098635 | biostudies-literature | 2011 May

REPOSITORIES: biostudies-literature

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Gene editing of human embryonic stem cells via an engineered baculoviral vector carrying zinc-finger nucleases.

Lei Yuning Y   Lee Chi-Lin CL   Joo Kye-Il KI   Zarzar Jonathan J   Liu Yarong Y   Dai Bingbing B   Fox Victoria V   Wang Pin P  

Molecular therapy : the journal of the American Society of Gene Therapy 20110215 5


Human embryonic stem (hES) cells are renewable cell sources that have potential applications in regenerative medicine. The development of technologies to produce permanent and site-specific genome modifications is in demand to achieve future medical implementation of hES cells. We report herein that a baculoviral vector (BV) system carrying zinc-finger nucleases (ZFNs) can successfully modify the hES cell genome. BV-mediated transient expression of ZFNs specifically disrupted the CCR5 locus in t  ...[more]

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