Detection of Sleeping Beauty transposition in the genome of host cells by non-radioactive Southern blot analysis

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• 作者：Rajagopal N. Aravalli^a ; ¹ ; ^{aravalli@umn.edu" class="auth_mail" title="E-mail the corresponding author} ; Chang W. Park^b ; ¹ ; Clifford J. Steer^b ; ^c ; ^{steer001@umn.edu" class="auth_mail" title="E-mail the corresponding author}
• 关键词：Epigenetic ; Methylation ; Sleeping Beauty ; SB100X ; Southern blot ; Transposon
• 刊名：Biochemical and Biophysical Research Communications
• 出版年：2016
• 出版时间：26 August 2016
• 年：2016
• 卷：477
• 期：3
• 页码：317-321
• 全文大小：749 K

文摘

The Sleeping Beauty transposon (SB-Tn) system is being used widely as a DNA vector for the delivery of therapeutic transgenes, as well as a tool for the insertional mutagenesis in animal models. In order to accurately assess the insertional potential and properties related to the integration of SB it is essential to determine the copy number of SB-Tn in the host genome. Recently developed SB100X transposase has demonstrated an integration rate that was much higher than the original SB10 and that of other versions of hyperactive SB transposases, such as HSB3 or HSB17. In this study, we have constructed a series of SB vectors carrying either a DsRed or a human β-globin transgene that was encompassed by cHS4 insulator elements, and containing the SB100X transposase gene outside the SB-Tn unit within the same vector in cis configuration. These SB-Tn constructs were introduced into the K-562 erythroid cell line, and their presence in the genomes of host cells was analyzed by Southern blot analysis using non-radioactive probes. Many copies of SB-Tn insertions were detected in host cells regardless of transgene sequences or the presence of cHS4 insulator elements. Interestingly, the size difference of 2.4 kb between insulated SB and non-insulated controls did not reflect the proportional difference in copy numbers of inserted SB-Tns. We then attempted methylation-sensitive Southern blots to assess the potential influence of cHS4 insulator elements on the epigenetic modification of SB-Tn. Our results indicated that SB100X was able to integrate at multiple sites with the number of SB-Tn copies larger than 6 kb in size. In addition, the non-radioactive Southern blot protocols developed here will be useful to detect integrated SB-Tn copies in any mammalian cell type.