hESC engineering by integrase-mediated chromosomal targeting.

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Abstract

Bacteriophage recombinases can target specific loci in human embryonic stem cells (hESCs) at high efficiency allowing for long-term expression of transgenes. In this chapter, we describe a retargeting system where phiC31 integrase is used to deliver a chromosomal target for a second integrase, R4. The engineered hESC line can be adapted for complex element assembly using Multisite Gateway technology. Retargeted clones show sustained expression and appropriate regulation of the transgenes over long-term culture and upon differentiation. The system described here represents a method to rapidly assemble complex plasmid-based assay systems, controllably insert them into the hESC genome, and have them actively express in pluripotent as well as in differentiated lineages there from.

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Liu, Y., Lakshmipathy, U., Ozgenc, A., Thyagarajan, B., Lieu, P., Fontes, A., … Chesnut, J. D. (2010). hESC engineering by integrase-mediated chromosomal targeting. Methods in Molecular Biology (Clifton, N.J.), 584, 229–268. https://doi.org/10.1007/978-1-60761-369-5_13

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