P85gag-mos encoded by ts110 Moloney murine sarcoma virus has an associated protein kinase activity
AUTOR(ES)
Kloetzer, William S.
RESUMO
A protein identified as P85gag-mos was shown to be phosphorylated when immunoprecipitates from ts110 Moloney murine sarcoma virus transformed nonproducer cells (clone 6m2) were incubated with [γ-32P]ATP. The in vitro-labeled 85,000-dalton phosphoprotein comigrated on NaDodSO4/polyacrylamide gels with authentic phosphorylated P85gag-mos. Immunoprecipitates obtained with antisera prepared against Rauscher murine leukemia virus core protein p30 were active in the immune complex kinase assay but anti-murine leukemia virus p10 precipitates were not. Previous studies have shown that anti-p30 but not anti-p10 antisera recognize P85gag-mos. The 6m2 clone has been shown to express P85gag-mos at 33°C but not at 39°C. Anti-p30 immune complexes from 6m2 cells maintained at 39°C failed to phosphorylate the 85,000-dalton protein. Furthermore, the in vitro phosphorylated 85,000-dalton protein gave the same pattern of V8 protease-generated cleavage products as in vivo32P-labeled P85gag-mos. We conclude from these results that P85gag-mos is phosphorylated in anti-p30 immune complex kinase reactions. Phosphoamino acid analyses indicated that the in vitro phosphorylated P85gag-mos contained phosphoserine and phosphothreonine. Our findings indicate that incubation of anti-p30 immunoprecipitates at 39°C drastically reduced, in a specific way, the kinase activity associated with P85gag-mos. This result and other data suggest that the kinase is virus-encoded. Because P85gag-mos, but not Pr65gag is phosphorylated in anti-p30 immunoprecipitates from MuLV-MuSV ts110 producer cells, the kinase enzyme is associated with P85gag-mos and not gag gene products. A second major polypeptide of the size of P58gag was also phosphorylated in anti-p30 immunoprecipitates from cells maintained at 33°C but not at 39°C. Since 6m2 cells at 39°C contain P58gag, this is also consistent with the kinase activity being associated with P85gag-mos.
ACESSO AO ARTIGO
http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=393387Documentos Relacionados
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