Improved gene correction efficiency with a tailed duplex DNA fragment

Hiroyuki Tsuchiya, Masayuki Uchiyama, Kazuhiro Hara, Yoshimichi Nakatsu, Teruhisa Tsuzuki, Hideo Inoue, Hideyoshi Harashima, Hiroyuki Kamiya

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12 Citations (Scopus)

Abstract

A 606-base single-stranded (ss) DNA fragment, prepared by restriction enzyme digestion of ss phagemid DNA, corrects a hygromycin resistance and enhanced green fluorescent protein (Hyg-EGFP) fusion gene more efficiently than a PCR fragment, which is the conventional type of DNA fragment used in gene correction. Here, a tailed duplex, obtained by annealing an oligonucleotide to the ss DNA fragment, was used in the correction. The tailed duplex may be a good substrate for the RAD51 protein, an important enzyme in homologous recombination, which could be the gene correction pathway. The annealing of the oligonucleotides enhanced the correction efficiency of the Hyg-EGFP gene, especially when annealed in the 3′-region of the ss DNA fragment. Both the length and backbone structure of the oligonucleotides affected the gene correction efficiency. This type of gene correction device was also effective for another target gene, the rpsL gene. The results obtained in this study indicate that tailed duplex DNA fragments are effective nucleic acids for gene correction.

Original languageEnglish
Pages (from-to)8754-8759
Number of pages6
JournalBiochemistry
Volume47
Issue number33
DOIs
Publication statusPublished - Aug 19 2008

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All Science Journal Classification (ASJC) codes

  • Biochemistry

Cite this

Tsuchiya, H., Uchiyama, M., Hara, K., Nakatsu, Y., Tsuzuki, T., Inoue, H., ... Kamiya, H. (2008). Improved gene correction efficiency with a tailed duplex DNA fragment. Biochemistry, 47(33), 8754-8759. https://doi.org/10.1021/bi800588k