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Published on: July 24, 2011
Mechanisms of transformation by polyoma virus middle T antigen
D R Kaplan1, D C Pallas, W Morgan
1Dana-Farber Cancer Institute, Boston, MA 02115.
Abstract:
This review addresses a fundamental question of polyoma virus biology: What is the molecular mechanism by which the polyoma virus middle T antigen (MTAg) transforms cells in culture? Since MTAg has no known intrinsic biochemical activity, it is believed to act by modulating the properties of the host cell's proteins (see review by Courtneidge [26]). Experiments to date have largely focused on the interaction of MTAg with the cellular tyrosine kinase, pp60c-src. However, recent data from a number of laboratories have demonstrated the importance of other MTAg-associating cellular proteins in MTAg-mediated transformation, including pp62c-yes and a phosphatidylinositol kinase. In this review, we will summarize what is presently known about the proteins interacting with MTAg. The extent to which the currently known details of the biochemistry of MTAg and its associated proteins can explain the transforming properties of the various mutant alleles of MTAg will be assessed.
Insights
Polyoma virus middle T antigen (MTAg) transforms cells by interacting with host proteins. This review explores MTAg
Area of Science:
- Virology
- Molecular Biology
- Cellular Transformation
Background:
- Polyoma virus middle T antigen (MTAg) lacks intrinsic biochemical activity.
- MTAg is known to modulate host cell protein properties for transformation.
Purpose of the Study:
- To elucidate the molecular mechanisms of MTAg-mediated cell transformation.
- To review proteins interacting with MTAg and their role in transformation.
Main Methods:
- Literature review of experimental data on MTAg-protein interactions.
- Analysis of MTAg-associated cellular proteins, including pp60c-src, pp62c-yes, and phosphatidylinositol kinase.
Main Results:
- MTAg transformation involves interactions with multiple host proteins.
- Key interacting proteins include tyrosine kinase pp60c-src, pp62c-yes, and phosphatidylinositol kinase.
Conclusions:
- Understanding MTAg-protein interactions is crucial for explaining cell transformation.
- Biochemical details of MTAg and its associated proteins are assessed for their role in transforming properties of MTAg mutants.
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