A key role for the c-myc oncogene in cellular proliferation has long been postulated. C-myc may act by modulating the expression of other cellular genes whose products directly control proliferation. Permanent cell lines (in which the endogenous c- mYc gene is tightly regulated by growth factors and cell/cell contact) have been constructed in which expression of an exogenously transfected c-myc gene is controlled by the Drosophila heat shock 70 promoter. Transcription and subsequent translation of the exogenous c-myc gene is specifically induced by mild heat shock. The endogenous c-myc gene is not expressed under these conditions. Compared to heat-shocked cell lines which contain constructs lacking c-myc, several changes in cellular gene expression are observed: (1) two-dimensional analysis of the proteins from c-myc-containing cell lines shows the induction of eight protein species and the repression of five protein species relative to cell lines lacking c-myc; (2) the transcripts of two genes (3CH77 and 3CH92) previously identified as serum inducible are induced when c-myc is expressed; (3) the endogenous heat shock 70 gene may be specifically induced in response to c-myc. Therefore, c-myc expression alters the expression of other cellular genes, including the induction of some known to be expressed only in proliferating cells.

Agency
National Institute of Health (NIH)
Institute
Division of Cancer Epidemiology And Genetics (NCI)
Type
Intramural Research (Z01)
Project #
1Z01CP005569-02
Application #
3916920
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
2
Fiscal Year
1988
Total Cost
Indirect Cost
Name
Cancer Epidemiology and Genetics
Department
Type
DUNS #
City
State
Country
United States
Zip Code