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PMID: 10321733 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

RBP1 induces growth arrest by repression of E2F-dependent transcription.

Oncogene ·Vol. 18 ·No. 12 ·1999-03-25 ·Pages 2091-100

Lai A, Marcellus RC, Corbeil HB, Branton PE

Abstract

Growth arrest and cell cycle progression are regulated by the retinoblastoma tumour suppressor pRB and related proteins p130 and p107 that bind to and inhibit the E2F family of transcription factors. Although the precise mechanism of this inhibition remains to be established, previous studies indicated the presence of transcriptional repression activity in the 'pocket' of RB family members. We show here that RBP1, a known pRB pocket-binding protein, possesses transcriptional repression activity and associates with p130-E2F and pRB-E2F complexes specifically during growth arrest. Overexpression of RBP1 both inhibited E2F-dependent gene expression and suppressed cell growth. Thus repression of E2F-dependent transcription by RBP1 via RB family members may play a central role in inducing growth arrest.

MeSH Terms
Animals CHO Cells Carrier Proteins/genetics,metabolism Cell Cycle/genetics Cell Cycle Proteins Cricetinae DNA-Binding Proteins E2F Transcription Factors Gene Expression Regulation Humans Protein Binding Repressor Proteins/metabolism Retinoblastoma Protein/genetics,metabolism Retinoblastoma-Binding Protein 1 Transcription Factor DP1 Transcription Factors/metabolism Transcription, Genetic
Chemicals
Carrier Proteins Cell Cycle Proteins DNA-Binding Proteins E2F Transcription Factors Repressor Proteins Retinoblastoma Protein Retinoblastoma-Binding Protein 1 Transcription Factor DP1 Transcription Factors
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Lai A
Department of Biochemistry, McGill University, Montreal, Quebec, Canada.
Marcellus R C
Corbeil H B
Branton P E
Article Info
Journal
Oncogene
Abbr.
Oncogene
ISSN
0950-9232
Published
1999-03-25
Pages
2091-100
Language
English
Region
England
NLM ID
8711562
Subset
IM
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