Kaplan D R, Whitman M, Schaffhausen B, Raptis L, Garcea R L, Pallas D, Roberts T M, Cantley L
Proc Natl Acad Sci U S A. 1986 Jun;83(11):3624-8. doi: 10.1073/pnas.83.11.3624.
The effect of polyoma middle-sized tumor antigen (MTAg) on phosphatidylinositol metabolism has been characterized in vivo and in vitro using polyoma-transformed and polyoma-infected cells. Cells infected with transformation-competent polyoma virus exhibit increased levels of inositol phospholipids and the second messenger inositol trisphosphate. MTAg or pp60c-src immunoprecipitates from MTAg-transformed cells contain an activity that phosphorylates phosphatidylinositol and phosphatidylinositol 4-phosphate. This activity is induced in parallel with MTAg when the MTAg synthesis is regulated by hormonal or heavy metal inducers. Immunoprecipitates from one class of polyoma mutants defective in transformation have a reduced level of associated phosphatidylinositol kinase activity in vitro yet are capable of tyrosine phosphorylation on exogenous protein substrates at rates comparable to wild-type virus. Thus, for these mutants, phosphatidylinositol kinase activity is more tightly correlated with transformation than is protein kinase activity. These results suggest that alterations in phosphatidylinositol metabolism by MTAg play a role in transformation by polyoma virus.
利用多瘤病毒转化细胞和感染细胞,在体内和体外对多瘤病毒中肿瘤抗原(MTAg)对磷脂酰肌醇代谢的影响进行了表征。感染具有转化能力的多瘤病毒的细胞中,肌醇磷脂和第二信使三磷酸肌醇的水平升高。从MTAg转化细胞中免疫沉淀的MTAg或pp60c-src含有使磷脂酰肌醇和磷脂酰肌醇4-磷酸磷酸化的活性。当MTAg的合成受激素或重金属诱导剂调节时,这种活性与MTAg平行诱导。一类转化缺陷的多瘤病毒突变体的免疫沉淀物在体外的相关磷脂酰肌醇激酶活性水平降低,但能够以与野生型病毒相当的速率对外源蛋白质底物进行酪氨酸磷酸化。因此,对于这些突变体,磷脂酰肌醇激酶活性比蛋白激酶活性与转化的相关性更强。这些结果表明,MTAg引起的磷脂酰肌醇代谢改变在多瘤病毒的转化中起作用。