Cancer gene discovery in solid tumours using transposon-based somatic mutagenesis in the mouse

Nature. 2005 Jul 14;436(7048):272-6. doi: 10.1038/nature03681.

Abstract

Retroviruses, acting as somatic cell insertional mutagens, have been widely used to identify cancer genes in the haematopoietic system and mammary gland. An insertional mutagen for use in other mouse somatic cells would facilitate the identification of genes involved in tumour formation in a wider variety of tissues. Here we report the ability of the Sleeping Beauty transposon to act as a somatic insertional mutagen to identify genes involved in solid tumour formation. A Sleeping Beauty transposon, engineered to elicit loss-of-function or gain-of-function mutations, transposed in all somatic tissues tested and accelerated tumour formation in mice predisposed to cancer. Cloning transposon insertion sites from these tumours revealed the presence of common integration sites, at known and candidate cancer genes, similar to those observed in retroviral mutagenesis screens. Sleeping Beauty is a new tool for unbiased, forward genetic screens for cancer genes in vivo.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • DNA Transposable Elements / genetics
  • Genetic Testing / methods*
  • Genetic Vectors / genetics
  • Mice
  • Mice, Transgenic
  • Mutagenesis, Insertional / genetics*
  • NIH 3T3 Cells
  • Neoplasms / genetics*
  • Oncogenes / genetics*
  • Proto-Oncogene Proteins B-raf / genetics
  • Proto-Oncogene Proteins B-raf / metabolism
  • Sarcoma / genetics

Substances

  • DNA Transposable Elements
  • Braf protein, mouse
  • Proto-Oncogene Proteins B-raf