Abstract
In this report, we demonstrate the feasibility of transforming mouse cells deficient in adenine phosphoribosyltransferase (aprt; AMP:pyrophosphate phosphoribosyltransferase, EC 2.4.2.7) to the aprt+ phenotype by means of DNA-mediated gene transfer. Transformation was effected by using unfractionated high molecular weight genomic DNA from Chinese hamster, human, and mouse cells and restriction endonuclease-digested DNA from rabbit liver. The transformation frequency observed was between 1 and 10 colonies per 10(6) cells per 20 microgram of donor DNA. Transformants displayed enzymatic activity that was donor derived as demonstrated by isoelectric focusing of cytoplasmic extracts. These transformants fall into two classes: those that are phenotypically stable when grown in the absence of selective pressure and those that are phenotypically unstable under the same conditions.
MeSH Terms
Adenine Phosphoribosyltransferase/genetics,metabolism
Animals
Cell Line
Clone Cells
Cricetinae
DNA Restriction Enzymes
DNA, Recombinant/metabolism
HeLa Cells/metabolism
Humans
Mice
Molecular Weight
Pentosyltransferases/genetics
Phenotype
Salmon
Transformation, Genetic
Chemicals
DNA, Recombinant
Pentosyltransferases
Adenine Phosphoribosyltransferase
DNA Restriction Enzymes
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Wigler M
Pellicer A
Silverstein S
Axel R
Urlaub G
Chasin L
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13 references, click to expand
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