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pubmed-article:10328848pubmed:abstractTextTo trace cell lineages and the origin and fate of cells in transplantation and embryo chimeras, a DNA/DNA in situ hybridization cell labelling system was developed, based on a 50-copy murine c-myc transgene on mouse chromosome 8. Elevated levels of cMyc mRNA were found in Myc*tg50 (Myctg50/0 and Myctg50/Myctg50) transgenic tissues, but adult transgenic NMRI mice were anatomically and histologically indistinguishable from control NMRI mice and did not develop tumours on a wild-type or nude (nu/nu) background. The hybridization label detected transgenic nuclei with an efficiency of approximately 80%. In muscle grafts, this transgene label was successfully applied to trace donor cells in a labelled host and to study the invasion of a graft by host cells. When the cMyc hybridization was used in allophenic mice of the control<-->NMRI-Myctg50/? (nu/+ or +/+) type, an up to a three-fold excess of MYC*tg50 positive over control nuclei was found in all organs examined (ventricle, skeletal muscle, liver, small intestine). This overgrowth of MYC*tg50 cells is probably due to transgene expression. Four out of seven (C57BL/6xBALB/c) or (C57BL/6xNMRI)<-->MYC*tg50 allophenic mice displayed anatomical abnormalities, e.g. an enlarged thymus and a tumour in the groin region. As these abnormalities were only observed in allophenic mice, they might be due to the imbalance of growth potential between MYC*tg50 transgenic and normal cells in the same individual.lld:pubmed
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pubmed-article:10328848pubmed:copyrightInfoCopyright 1998 Academic Press.lld:pubmed
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pubmed-article:10328848pubmed:dateRevised2006-11-15lld:pubmed
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pubmed-article:10328848pubmed:articleTitleA multicopy c-Myc transgene as a nuclear label: overgrowth of Myctg50 cells in allophenic mice.lld:pubmed
pubmed-article:10328848pubmed:affiliationDevelopmental Biology and Molecular Pathology, University of Bielefeld, Bielefeld, D-33501, Germany.lld:pubmed
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pubmed-article:10328848pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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