Efficiency and Specificity of Targeted Integration Mediated by the Adeno-Associated Virus Serotype 2 Rep 78 Protein

被引:3
作者
Li, Pingjuan [1 ,2 ]
Marino, Michael P. [1 ]
Zou, Jizhong [3 ]
Argaw, Takele [1 ]
Morreale, Michael T. [1 ]
Iaffaldano, Brian J. [1 ]
Reiser, Jakob [1 ]
机构
[1] US FDA, Div Cellular & Gene Therapies, Ctr Biol Evaluat & Res, 10903 New Hampshire Ave,Bldg 52-72,Room 3106, Silver Spring, MD 20993 USA
[2] Gemini Therapeut Inc, Cambridge, MA USA
[3] NHLBI, NIH, Bldg 10, Bethesda, MD 20892 USA
关键词
AAVS1; locus; site-specific integration; site-specific nuclease; DNA nickase; integrase-defective lentiviral vectors; human iPSCs; SITE-SPECIFIC INTEGRATION; LENTIVIRAL VECTORS; HUMAN GENOME; HUMAN-CELLS; RECOMBINATION; LOCUS; AAV; RNA; CHROMOSOME-19; ENDONUCLEASE;
D O I
10.1089/hgtb.2018.052
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
The adeno-associated virus serotype 2 (AAV2) Rep 78 protein, a strand-specific endonuclease (nickase) promotes site-specific integration of transgene sequences bearing homology arms corresponding to the AAVS1 safe harbor locus. To investigate the efficiency and specificity of this approach, plasmid-based donor vectors were tested in concert with nuclease encoding vectors, including an engineered version of the AAV2 Rep 78 protein, an AAVS1-specific zinc finger nuclease (ZFN), and the CRISPR-Cas9 components in HEK 293 cells. The Rep 78 and ZFN-based approaches were also compared in HEK 293 cells and in human induced pluripotent stem cells using integrase deficient lentiviral vectors. The targeting efficiencies involving the Rep 78 protein were similar to those involving the AAVS1-specific ZFN, while the targeting specificity for the Rep 78 protein was lower compared to that of the ZFN. It is anticipated that the Rep 78 nickase-based targeting approach may ultimately contribute to the reduction of risks associated with other genome editing approaches involving DNA double-strand breaks.
引用
收藏
页码:135 / 145
页数:11
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