Separation of simian virus 40 large-T-antigen-transforming and origin-binding functions from the ability to block differentiation
- PMID: 2835674
- PMCID: PMC363287
- DOI: 10.1128/mcb.8.3.1380-1384.1988
Separation of simian virus 40 large-T-antigen-transforming and origin-binding functions from the ability to block differentiation
Abstract
Wild-type simian virus 40 large T antigen is very effective at blocking adipocyte differentiation in 3T3-F442A cells as assayed by triglyceride accumulation, induction of glycerophosphate dehydrogenase activity, and expression of mRNAs for glycerophosphate dehydrogenase, the adipocyte serine protease adipsin, and the putative lipid-binding protein adipocyte P2. Point mutants defective for either origin-specific DNA binding or transformation blocked differentiation as completely as wild type.
References
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources