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      Induction of transgene expression in Tg.AC(v-Ha-ras) transgenic mice concomitant with DNA hypomethylation.

      Molecular carcinogenesis
      Animals, Cell Transformation, Neoplastic, genetics, DNA Methylation, Female, Gene Expression Regulation, Genes, ras, Globins, Mice, Mice, Transgenic, Oncogene Protein p21(ras), biosynthesis, physiology, Papilloma, etiology, Polymerase Chain Reaction, Simian virus 40, Skin, injuries, Skin Neoplasms, Transcription, Genetic, Transgenes, Wound Healing, Wounds and Injuries, complications

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          Abstract

          Tg.AC transgenic mice have a transgene composed of a zeta-globin transcriptional control region, a v-Ha-ras coding region, and a simian virus 40 3' polyadenylation signal sequence. Induced ectopic expression of the transgene by chemical treatment or full-skin-thickness wounding leads to the development of skin papillomas. Reverse transcription-polymerase chain reaction assays and protein blotting indicated that the transgene was expressed 16-28 d after full-skin-thickness surgical wounding. Normal unwounded skin did not express the transgene. DNA blotting indicated that the position of the transgene remained stable during wound-induced tumorigenesis. Concomitant with the v-Ha-ras mRNA and protein expression was the hypomethylation of specific MspI/HpaII sites within the transgene. These results are consistent with the hypothesis that hypomethylation is required for the induced and sustained expression of the Tg.AC v-Ha-ras transgene in spontaneous and induced tumors in Tg.AC mice.

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