Abstract
Transposable elements are DNA sequences with the ability to move from one genomic location to another. The movement of class II transposable elements has been functionally harnessed and separated into two distinct DNA transposon components: the terminal inverted repeat sequences that flank genetic cargo to be mobilized and a transposase enzyme capable of recognizing the terminal inverted repeat sequences and catalyzing the transposition reaction. In particular, the Sleeping Beauty (SB) system was the first successful demonstration of transposon-based gene transfer in vertebrate species. Over the years, several improvements have been made to SB technology and more recent studies have demonstrated the versatility of the system for many applications including insertional mutagenesis, gene transfer, and transgenesis. These genetic engineering advances made available by SB both augment and advance large-scale efforts that have been directed toward identifying how genes and environmental factors influence human health in recent years. In the age of personalized medicine, the versatility of SB provides numerous genetic engineering avenues for answering novel questions in basic and applied research. This chapter discusses the use of SB-based insertional mutagenesis in mice for the efficient identification of candidate cancer genes across numerous types of cancers.
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References
Wang Z, Jensen MA, Zenklusen JC (2016) A practical guide to the Cancer genome atlas (TCGA). Methods Mol Biol 1418:111–141
Dupuy AJ (2010) Transposon-based screens for cancer gene discovery in mouse models. Semin Cancer Biol 20(4):261–268
Muñoz-López M, García-Pérez JL (2010) DNA transposons: nature and applications in genomics. Curr Genomics 11(2):115–128
Ammar I, Izsvak Z, Ivics Z (2012) The sleeping beauty transposon toolbox. Methods Mol Biol 859:229–240
Plasterk RH (1996) The Tc1/mariner transposon family. Curr Top Microbiol Immunol 204:125–143
Moriarity BS, Largaespada DA (2015) Sleeping beauty transposon insertional mutagenesis based mouse models for cancer gene discovery. Curr Opin Genet Dev 30:66–72
Izsvak Z, Ivics Z (2005) Sleeping beauty hits them all: transposon-mediated saturation mutagenesis in the mouse germline. Nat Methods 2(10):735–736
Ivics Z et al (1997) Molecular reconstruction of sleeping beauty, a Tc1-like transposon from fish, and its transposition in human cells. Cell 91(4):501–510
Collier LS et al (2005) Cancer gene discovery in solid tumours using transposon-based somatic mutagenesis in the mouse. Nature 436(7048):272–276
Kool J, Berns A (2009) High-throughput insertional mutagenesis screens in mice to identify oncogenic networks. Nat Rev Cancer 9(6):389–399
Brett BT et al (2011) Novel molecular and computational methods improve the accuracy of insertion site analysis in sleeping beauty-induced tumors. PLoS One 6(9):e24668
Acknowledgments
Author B.A.S. is supported by NIH/NIAMS T32 AR050938 “Musculoskeletal Training Grant.” Author B.S.M. is supported by funding from the American Association for Cancer Research (AACR), Children’s Cancer Research Fund (CCRF), Karen Wyckoff Rein in Sarcoma Foundation (KWRIS) and The Randy Shaver Foundation.
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Becklin, K.L., Smeester, B.A., Moriarity, B.S. (2019). Cancer Gene Discovery Utilizing Sleeping Beauty Transposon Mutagenesis. In: Starr, T. (eds) Cancer Driver Genes. Methods in Molecular Biology, vol 1907. Humana Press, New York, NY. https://doi.org/10.1007/978-1-4939-8967-6_13
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DOI: https://doi.org/10.1007/978-1-4939-8967-6_13
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