We have introduced a specific point mutation into the gene for chromosomal elongation factor 2 (EF-2) in Chinese hamster ovary cells (CHO-K1) by in vivo homologous recombination. To obtain a selectable construct for gene-targeting, we modified a diphtheria toxin-resistant mutant EF-2 gene (Gly717 to Arg) by deleting its promoter and first exon so that homologous recombinants could be distinguished from randomly integrated transformants, and also by inserting a second positive selection marker, the neomycin-resistance gene, into the 3′-flanking region to increase the selective accuracy. More than 80% of the clones surviving after selection for resistance to both the toxin and neomycin were the desired homologous recombinants in which the wild-type, toxin-sensitive EF-2 gene was replaced by the modified gene giving resistance to both the toxin and neomycin. This result shows that the specific point mutation was co-introduced with a second selective marker into an endogenous chromosomal gene and that the modified gene was expressed. © 1991, Japan Society for Cell Biology. All rights reserved.
CITATION STYLE
Kido, M., Kohno, K., Uchida, T., Okada, Y., & Miwatani, H. (1991). Targeted Introduction of a Diphtheria Toxin-Resistant Point Mutation into the Chromosomal EF-2 Locus by in vivo Homologous Recombination. Cell Structure and Function, 16(6), 447–453. https://doi.org/10.1247/csf.16.447
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