NDLI: E2F4-RB and E2F4-p107 complexes suppress gene expression by transforming growth factor beta through E2F binding sites.

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E2F4-RB and E2F4-p107 complexes suppress gene expression by transforming growth factor beta through E2F binding sites.

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E2F4-RB and E2F4-p107 complexes suppress gene expression by transforming growth factor beta through E2F binding sites.

Content Provider	World Health Organization (WHO)-Global Index Medicus
Author	Yu, Y. Wang, X. F. Li, J. M. Hu, P. P. Shen, X.
Description	Author Affiliation: Li JM ( Department of Pharmacology, Duke University Medical Center, Durham, NC 27708, USA.);
Abstract	Transforming growth factor beta (TGF-beta) causes growth arrest in most cell types. TGF-beta induces hypophosphorylation of retinoblastoma susceptibility gene 1 product (RB), which sequesters E2F factors needed for progression into S phase of the cell cycle, thereby leading to cell cycle arrest at G1. It is possible, however, that the E2F-RB complex induced by TGF-beta may bind to E2F sites and suppress expression of specific genes whose promoters contain E2F binding sites. We show here that TGF-beta treatment of HaCaT cells induced the formation of E2F4-RB and E2F4-p107 complexes, which are capable of binding to E2F sites. Disruption of their binding to DNA with mutation in the E2F sites did not change the expression from promoters of E2F1, B-myb, or HsORC1 genes in cycling HaCaT cells. However, the same mutation stimulated 5- to 6-fold higher expression from all three promoters in cells treated with TGF-beta. These results suggest that E2F binding sites play an essential role in the transcription repression of these genes under TGF-beta treatment. Consistent with their repression of TGF-beta-induced gene expression, introduction of E2F sites into the promoter of cyclin-dependent kinase inhibitor p15(INK4B) gene effectively inhibited its induction by TGF-beta. Experiments utilizing Gal4-RB and Gal4-p107 chimeric constructs demonstrated that either RB or p107 could directly repress TGF-beta induction of p15(INK4B) gene when tethered to p15(INK4B) promoter through Gal4 DNA binding sites. Therefore, E2F functions to bring RB and p107 to E2F sites and represses gene expression by TGF-beta. These results define a specific function for E2F4-RB and E2F4-p107 complexes in gene repression under TGF-beta treatment, which may constitute an integral part of the TGF-beta-induced growth arrest program.
ISSN	00278424
e-ISSN	10916490
Journal	Proceedings of the National Academy of Sciences of the United States of America
Issue Number	10
Volume Number	94
Language	English
Publisher	National Academy of Sciences
Publisher Date	1997-06-01
Publisher Place	United States
Access Restriction	Open
Subject Keyword	Cyclin-Dependent Kinase Inhibitor P16 DNA-Binding Proteins Metabolism Nuclear Proteins Retinoblastoma Protein Transcription Factors Transcription, Genetic Physiology Transforming Growth Factor Beta Pharmacology Tumor Suppressor Proteins Binding Sites Carrier Proteins Biosynthesis Cell Cycle Cell Cycle Proteins Cell Line Cyclin-Dependent Kinase Inhibitor P15 Isolation & Purification E2F Transcription Factors E2F1 Transcription Factor E2F4 Transcription Factor Keratinocytes Oligodeoxyribonucleotides Promoter Regions, Genetic Protein Binding Recombinant Fusion Proteins Retinoblastoma-Binding Protein 1 Retinoblastoma-Like Protein P107 Transcription Factor DP1 Drug Effects Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S. Multidisciplinary
Content Type	Text
Resource Type	Article
Subject	Multidisciplinary

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