Target-site Preferences of Sleeping Beauty Transposons

The Sleeping Beauty (SB) transposon is a Tc1/ mariner family transposon that has applications in vertebrate animals for gene transfer, gene-tagging, and human gene therapy. In this study, we analyzed the target-site preferences of the SB transposon. At the genomic level, integration of SB transposon...

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Veröffentlicht in:Journal of molecular biology 2005-02, Vol.346 (1), p.161-173
Hauptverfasser: Liu, Geyi, Geurts, Aron M., Yae, Kojiro, Srinivasan, A.R., Fahrenkrug, Scott C., Largaespada, David A., Takeda, Junji, Horie, Kyoji, Olson, Wilma K., Hackett, Perry B.
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Sprache:eng
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Zusammenfassung:The Sleeping Beauty (SB) transposon is a Tc1/ mariner family transposon that has applications in vertebrate animals for gene transfer, gene-tagging, and human gene therapy. In this study, we analyzed the target-site preferences of the SB transposon. At the genomic level, integration of SB transposons with respect to genes (exons and introns) and intergenic regions appears fairly random but not on a micro-scale. Although there appears to be a consensus sequence around the vicinity of the target sites, the primary sequence is not the determining factor for target selection. When integrations were examined over a limited topography, the sites used most often for integration did not match the consensus sequence. Rather, a unique deformation inherent in the sequence may be a recognition signal for target selection. The deformation is characterized by an angling of the target site such that the axis around the insertion site is off-center, the rotation of the helix (twisting) is non-uniform and there is an increase in the distance between the central base-pairs. Our observations offer several hypothetical insights into the transposition process. Our observations suggest that particular deformations of the double helix predicted by the V step algorithm can distinguish TA sites that vary by about 16-fold in their preferences for accommodating insertions of SB transposons.
ISSN:0022-2836
1089-8638
DOI:10.1016/j.jmb.2004.09.086