Enhancement of cellular src gene product associated tyrosyl kinase activity following polyoma virus infection and transformation.

Abstract:

:We examine the interaction between polyoma-virus-encoded middle tumor antigen and the cellular src gene product, pp60c-src, using a series of monoclonal antibodies that recognize mammalian pp60c-src. Our results show that infection of mouse cells with transformation-competent strains of polyoma virus results in the stimulation of pp60c-src kinase activity severalfold over that observed in uninfected mouse cells and mouse cells infected with transformation-deficient polyoma virus. A similar degree of enhancement of pp60c-src kinase activity was found in polyoma-virus-transformed rodent cells. No differences were detected in the level of pp60c-src synthesis in polyoma-virus-infected and uninfected mouse cells or polyoma-virus-transformed and normal rodent cells. These studies demonstrate that polyoma-virus-encoded middle tumor antigen is associated with pp60c-src in lysates of polyoma-virus-infected and polyoma-virus-transformed cells and suggest a novel mechanism for the functional activation of a cellular proto-oncogene product, namely, that the interaction between middle tumor antigen and pp60c-src leads to a stimulation of pp60c-src tyrosyl kinase activity.

journal_name

Cell

journal_title

Cell

authors

Bolen JB,Thiele CJ,Israel MA,Yonemoto W,Lipsich LA,Brugge JS

doi

10.1016/0092-8674(84)90272-1

subject

Has Abstract

pub_date

1984-10-01 00:00:00

pages

767-77

issue

3

eissn

0092-8674

issn

1097-4172

pii

0092-8674(84)90272-1

journal_volume

38

pub_type

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