1. Mouse Cancer Genetics Program, National Cancer Institute, Center for Cancer Research, Frederick, Maryland 21702, USA
2. Department of Genetics, Cell Biology and Development, Arnold and Mabel Beckman Center for Transposon Research, The Cancer Center, University of Minnesota, Minneapolis, Minnesota 55455, USA

Correspondence to: Nancy A. Jenkins¹ Correspondence and requests for materials should be addressed to N.A.J. (Email: jenkins@ncifcrf.gov).

Abstract

Transposons have provided important genetic tools for functional genomic screens in lower eukaryotes but have proven less useful in higher eukaryotes because of their low transposition frequency. Here we show that Sleeping Beauty (SB), a member of the Tc1/mariner class of transposons, can be mobilized in mouse somatic cells at frequencies high enough to induce embryonic death and cancer in wild-type mice. Tumours are aggressive, with some animals developing two or even three different types of cancer within a few months of birth. The tumours result from SB insertional mutagenesis of cancer genes, thus facilitating the identification of genes and pathways that induce disease. SB transposition can easily be controlled to mutagenize any target tissue and can therefore, in principle, be used to induce many of the cancers affecting humans, including those for which little is known about the aetiology. The uses of SB are also not restricted to the mouse and could potentially be used for forward genetic screens in any higher eukaryote in which transgenesis is possible.

1. Mouse Cancer Genetics Program, National Cancer Institute, Center for Cancer Research, Frederick, Maryland 21702, USA
2. Department of Genetics, Cell Biology and Development, Arnold and Mabel Beckman Center for Transposon Research, The Cancer Center, University of Minnesota, Minneapolis, Minnesota 55455, USA

Correspondence to: Nancy A. Jenkins¹ Correspondence and requests for materials should be addressed to N.A.J. (Email: jenkins@ncifcrf.gov).

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