Assuntos
Apoptose/fisiologia , Interferon gama/farmacologia , Triptofano/metabolismo , Trifosfato de Adenosina/metabolismo , Apoptose/efeitos dos fármacos , Calcimicina/farmacologia , Linhagem Celular , DNA/análise , Eletroforese em Gel de Ágar , Células HL-60 , Humanos , Cinética , Fosforilação , Proteínas Serina-Treonina Quinases/metabolismo , Triptofano Oxigenase/efeitos dos fármacos , Triptofano Oxigenase/metabolismo , eIF-2 QuinaseRESUMO
An adenovirus-5 recombinant virus Adapt1 carrying the Chinese hamster ovary (CHO) adenine phosphoribosyltransferase (aprt) gene was constructed by insertion of a 2.5-kb fragment containing the complete CHO aprt structural gene linked to a Moloney murine sarcoma virus (MSV) promoter into the E3 region of adenovirus-5. The CHO aprt gene was in the opposite orientation to the adenovirus E3 promoter. Mouse Lapt- tk- (LAT) cells expressed the CHO aprt gene when infected with the virus, even at low MOI (O.1). APRT activity was detectable from approximately 20 h postinfection. At a low frequency, LAT cells were transformed to aprt+, and four stable transductants were selected in adenine, azaserine (AA) medium. Such cells expressed APRT at approximately 50% wild-type activity and the enzyme was shown to be CHO APRT by starch gel electrophoresis. DNA was isolated from the transductants and probed with CHO aprt-specific DNA and with viral DNA probes. The results indicated that the CHO aprt gene was integrated into the LAT cells at a site other than mouse aprt. Although neighboring viral sequences were integrated and maintained in the transductants, viral sequences further upstream and downstream of the aprt gene were absent.