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PMID: 2660073 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Regulation of cell cycle duration by c-myc levels.

Oncogene ·Vol. 4 ·No. 6 ·1989-06-00 ·Pages 773-87

Karn J, Watson JV, Lowe AD, Green SM, Vedeckis W

Abstract

Early passage murine fibroblasts infected with retroviral vectors carrying human c-myc 'minigenes' express high levels of c-myc and have a dramatically shortened G1-phase of the cell cycle. Cells infected with viruses where c-myc is expressed from the viral LTR (MSN-4 virus) express more c-myc protein than cells infected with viruses where c-myc is expressed from the SV40 early promoter (NSM-7 virus). Populations of cells were infected with high titre viruses, selected for drug-resistance, pulse labelled with bromodeoxyuridine (BrdUrd) and chased in BrdUrd free media. This allows accurate, simultaneous, measurement of the rate of exit of unlabelled cells from G1 and progression of BrdUrd-labelled cells through S-phase. The length of the G1-phase in cell populations infected with the MSN-4 virus is 4.65 h, a reduction of nearly 30% compared to the G1-phase length of 6.50 h seen in cells infected with the VSN-2 control virus. Cells infected with NSM-7 virus show an intermediate phenotype and have a G1-phase of 5.25 h. The lengths of the S-phase (4.50 to 4.75 h) and G2 + M phases (2.75 h) were not significantly altered by exogenous c-myc expression. When chases are performed in growth-factor free media, the G1-phase of infected and non-infected cells is extended by approximately 2 h. Cells infected with the c-myc viruses continue to cycle more rapidly than uninfected cells. Growth factor-deprived cells, restimulated with serum, show similar alterations of the cell cycle kinetics. MSN-4 and NSM-7 infected cells, expressing high levels of c-myc, enter S-phase 2 to 4 h earlier, but less synchronously, than control cells, and sustain subsequent rounds of DNA synthesis, while control cells do not. However, cells carrying activated c-myc genes have nearly-normal morphologies and are not tumourgenic in syngenic mice. These results demonstrate that c-myc levels are rate limiting for events in G1, and the length of G1 varies proportionally with the level of exogenous c-myc expression.

MeSH Terms
Animals Blood Bromodeoxyuridine Cell Cycle Cell Line Cell Transformation, Viral Computer Simulation Culture Media/pharmacology Fibroblasts/analysis,cytology,microbiology Flow Cytometry Genetic Vectors Humans Immunoblotting Interphase Kinetics Mice Proto-Oncogene Proteins/analysis,biosynthesis,physiology Proto-Oncogene Proteins c-myc Proto-Oncogenes Retroviridae/genetics
Chemicals
Culture Media Proto-Oncogene Proteins Proto-Oncogene Proteins c-myc Bromodeoxyuridine
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Karn J
MRC Laboratory of Molecular Biology, Medical Research Council Centre, Cambridge, UK.
Watson J V
Lowe A D
Green S M
Vedeckis W
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
1989-06-00
Pages
773-87
Language
English
Region
England
NLM ID
8711562
Subset
IM
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