Abstract
The somatic cell hybrid C121, with chromosome 7 as its sole human component, arose when mouse macrophages SV40 genomes are integrated at 7q31-7q35. We show that hybrids with a reduced chromosome 7 component, but which retain markers linked to the cystic fibrosis locus, can be generated by direct in vivo tumor selection or following chromosome-mediated gene transfer and SV40-mediated cellular transformation. Our methods for chromosome fragmentation and fine-structure mapping can now be applied to the substantial number of SV40-transformed human cell lines, with independent chromosomal integration sites, already available. Our results also suggest that expression of human epidermal growth factor receptor augments the tumorigenic potential of the SV40-transformed C121 hybrid.
Original language | English |
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Pages (from-to) | 29-38 |
Number of pages | 10 |
Journal | Somatic Cell and Molecular Genetics |
Volume | 16 |
Issue number | 1 |
Publication status | Published - 1990 |
Keywords
- Animals
- Antigens
- Cell Line, Transformed
- Cell Transformation, Neoplastic
- Cell Transformation, Viral
- Chromosome Mapping
- Chromosomes, Human, Pair 7
- Cystic Fibrosis
- DNA Probes
- Genetic Techniques
- Humans
- Hybrid Cells
- Mice
- Proto-Oncogenes
- Receptor, Epidermal Growth Factor
- Repetitive Sequences, Nucleic Acid
- Simian virus 40
- Transfection