Abstract
E2F transcription factors play an important role in the regulation of cell cycle progression. We report here the cloning and characterization of an additional member of this family, E2F-6. E2F-6 lacks pocket protein binding and transactivation domains, and it is a potent transcriptional repressor that contains a modular repression domain at its carboxyl terminus. Overproduction of E2F-6 had no specific effect on cell cycle progression in asynchronously growing Saos2 and NIH 3T3 cells, but it inhibited entry into S phase of NIH 3T3 cells stimulated to exit G0. Taken together, these data suggest that E2F-6 can regulate a subset of E2F-dependent genes whose products are required for entry into the cell cycle but not for normal cell cycle progression.
MeSH Terms
3T3 Cells
Amino Acid Sequence
Animals
Base Sequence
Binding Sites
Cloning, Molecular
Consensus Sequence
DNA, Complementary
E2F6 Transcription Factor
HeLa Cells
Humans
Mice
Molecular Sequence Data
Recombinant Proteins/genetics,metabolism
Repressor Proteins/genetics,metabolism
Transcription Factors/genetics,metabolism
Transcription, Genetic
Chemicals
DNA, Complementary
E2F6 Transcription Factor
E2F6 protein, human
E2f6 protein, mouse
Recombinant Proteins
Repressor Proteins
Transcription Factors
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Gaubatz S
Dana-Farber Cancer Institute and Harvard Medical School, Boston, MA 02115, USA.
Wood J G
Livingston D M
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