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PMID: 12893818 Published · ppublish English Journal Article

Identification and characterization of E2F7, a novel mammalian E2F family member capable of blocking cellular proliferation.

The Journal of biological chemistry ·Vol. 278 ·No. 43 ·2003-10-24 ·Pages 42041-9

de Bruin A, Maiti B, Jakoi L, Timmers C, Buerki R, Leone G

Abstract

The mammalian E2F family of transcription factors plays a crucial role in the regulation of cellular proliferation, apoptosis, and differentiation. Consistent with its biological role in a number of important cellular processes, E2F regulates the expression of genes involved in cell cycle, DNA replication, DNA repair, and mitosis. It has proven difficult, however, to determine the specific roles played by the various known family members in these cellular processes. The work presented here now extends the complexity of this family even further by the identification of a novel E2F family member, which we now term E2F7. Like the expression of the known E2F activators, E2F1, E2F2, and E2F3, the expression of E2F7 is growth-regulated, at least in part, through E2F binding elements on its promoter, and its protein product is localized to the nucleus and associates with DNA E2F recognition sites with high affinity. A number of salient features, however, make this member unique among the E2F family. First, the E2F7 gene encodes a protein that possesses two distinct DNA-binding domains and that lacks a dimerization domain as well as a transcriptional activation and a retinoblastoma-binding domain. In contrast to the E2F activators, E2F7 can block the E2F-dependent activation of a subset of E2F target genes as well as mitigate cellular proliferation of mouse embryo fibroblasts. These findings identify E2F7 as a novel member of the mammalian E2F transcription factor family that has properties of a transcriptional repressor capable of negatively influencing cellular proliferation.

MeSH Terms
Animals Binding Sites Cell Division Cloning, Molecular DNA/metabolism DNA, Complementary/isolation & purification E2F7 Transcription Factor Embryo, Mammalian/cytology Fibroblasts/cytology,metabolism Gene Expression Regulation Mice Peptide Elongation Factor 2/genetics,metabolism,physiology Promoter Regions, Genetic Protein Structure, Tertiary Repressor Proteins/genetics,metabolism,physiology Response Elements Transfection
Chemicals
DNA, Complementary E2F7 Transcription Factor E2f7 protein, mouse Peptide Elongation Factor 2 Repressor Proteins DNA
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
de Bruin Alain
Human Cancer Genetics Program, Department of Molecular Virology, Immunology and Medical Genetics, The Ohio State University, Columbus, OH 43210, USA.
Maiti Baidehi
Jakoi Laszlo
Timmers Cynthia
Buerki Robin
Leone Gustavo
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2003-10-24
Epub
2003-00-31
Pages
42041-9
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
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