Abstract
Fusion of hypoxanthine phosphoribosyltransferase (HPRT)(-) rat hepatoma cells with HPRT(+) human fibroblasts yielded hybrid clones that grew in HAT selective medium and contained all the rat chromosomes and one to nine human chromosomes. Among the retained chromosomes was the human X chromosome. In all clones backselected in medium containing 8-azaguanine, human X chromosome was absent. Electrophoretic analysis revealed that, without exception, hybrid clones growing in HAT medium had an active HPRT enzyme, either human or rat, or both. When these clones were backselected in 8-azaguanine, they did not show HPRT enzyme activity. Hybrids that contained the human X chromosome also had human glucose-6-phosphate dehydrogenase. The observed reexpression of rat HPRT in hybrid cells derived from HPRT(-) rat cells suggests that a genetic factor from the human cell determined the expression of the rat structural gene for HPRT.
MeSH Terms
Adenine
Animals
Carcinoma, Hepatocellular
Cell Fusion
Clone Cells
Electrophoresis, Polyacrylamide Gel
Female
Fibroblasts
Genes
Glucosephosphate Dehydrogenase/analysis,biosynthesis
Humans
Hybrid Cells/enzymology
Hypoxanthines
Isoenzymes/analysis,biosynthesis
Karyotyping
Liver Neoplasms
Parainfluenza Virus 1, Human
Pentosyltransferases/analysis,biosynthesis
Rats
Chemicals
Hypoxanthines
Isoenzymes
Glucosephosphate Dehydrogenase
Pentosyltransferases
Adenine
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Croce C M
Bakay B
Nyhan W L
Koprowski H
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