ABSTRACT
A single-nucleotide polymorphism (SNP) in a human gene can alter the behavior of the corresponding protein, and thereby affect an individual's response to drug therapy. Here, we describe a novel dual-targeting approach for introducing an SNP of choice into virtually any gene, through the use of modified single-stranded oligonucleotides (MSSOs). We use this strategy to create SNPs in a human gene contained in a yeast artificial chromosome (YAC). In the dual-targeting protocol, two different MSSOs are designed to edit two different bases in the same cell. A change in one of these genes is selective while the other is non-selective. We show that the population identified by selective pressure is enriched for cells that bear an edited base at the nonselective site. YACs with human genomic inserts containing particular SNPs or haplotypes can be used for pharmacogenomic applications, in cell lines and in transgenic animals.
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Acknowledgements
We are grateful to Ken Peterson for the YAC, Mike Rice and Karen Krakowski for invaluable experimental ideas and support, and Ethan Signer for critical evaluation of this paper. This work was supported in part by grants from NIH (R01 DK56134) and NaPro BioTherapeutics.
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EB Kmiec has received a grant from NaPro BioTherapeutics. Other authors-none.
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van Brabant, A., Williams, J., Parekh-Olmedo, H. et al. Gene editing of a human gene in yeast artificial chromosomes using modified single-stranded DNA and dual targeting. Pharmacogenomics J 4, 175–183 (2004). https://doi.org/10.1038/sj.tpj.6500237
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DOI: https://doi.org/10.1038/sj.tpj.6500237
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