| First Author | Yamaguchi T | Year | 2012 |
| Journal | Biochem Biophys Res Commun | Volume | 425 |
| Issue | 2 | Pages | 297-303 |
| PubMed ID | 22842569 | Mgi Jnum | J:187160 |
| Mgi Id | MGI:5435621 | Doi | 10.1016/j.bbrc.2012.07.085 |
| Citation | Yamaguchi T, et al. (2012) Comparison of gene-trapping efficiency between retroviral and lentiviral vectors in mouse embryonic stem cells. Biochem Biophys Res Commun 425(2):297-303 |
| abstractText | Gene trapping is a method of inserting DNA into the genome at random, generating insertional mutations throughout the genome. The efficiency of retroviral gene trapping is not sufficient in part because of a strong preference for retroviral integration near transcription start sites. In contrast, lentiviral vectors strongly favor integration in the entire region of highly active genes, suggesting that lentiviral vectors would improve the efficiency of gene trapping. In this study, we constructed both lentiviral and retroviral gene-trap vectors and analyzed integration sites in mouse embryonic stem (ES) cells. The frequency of false-positive gene-trap events was about 12-fold higher for the retroviral vector compared to the lentiviral vector. Within intragenic regions, most of the retroviral vector integration sites were found in the 5' untranslated region, while the lentiviral vector integrated uniformly throughout transcriptional units. The trapping efficiency of unique genes was significantly higher for the lentiviral vector ( approximately 83%) than for the retroviral vector ( approximately 51%). Our data demonstrate that the lentiviral vector can trap the active genes more efficiently than the retroviral vector and will facilitate efficient generation of gene-trap libraries not only in ES cells but also in a wide variety of cell lines and primary cells. |
