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Two E2F Sites Control Growth-regulated and Cell Cycle-regulated Transcription of the Htf9-a/RanBP1 Gene through Functionally Distinct Mechanisms

Authors :
Patrizia Lavia
B Di Fiore
Giulia Guarguaglini
Antonella Palena
René Bernards
Ron M. Kerkhoven
Source :
Journal of biological chemistry, 274(15), 10339. American Society for Biochemistry and Molecular Biology, The Journal of biological chemistry, 274 (1999): 10339–10348. doi:10.1074/jbc.274.15.10339, info:cnr-pdr/source/autori:Di Fiore, B; Guarguaglini, G; Palena, A; Kerkhoven, RM; Bernards, R; Lavia, P/titolo:Two E2F sites control growth-regulated and cell cycle-regulated transcription of the Htf9-a%2FRanBP1 gene through functionally distinct mechanisms/doi:10.1074%2Fjbc.274.15.10339/rivista:The Journal of biological chemistry (Print)/anno:1999/pagina_da:10339/pagina_a:10348/intervallo_pagine:10339–10348/volume:274
Publication Year :
1999
Publisher :
Elsevier BV, 1999.

Abstract

The gene encoding Ran-binding protein 1 (RanBP1) is transcribed in a cell cycle-dependent manner. The RanBP1 promoter contains two binding sites for E2F factors, named E2F-c, located proximal to the transcription start, and E2F-b, falling in a more distal promoter region, We have now induced site-directed mutagenesis in both sites. We have found that the distal E2F-b site, together with a neighboring Spl element, actively controls up-regulation of transcription in S phase. The proximal E2F-c site plays no apparent role in cycling cells yet is required for transcriptional repression upon growth arrest. Protein binding studies suggest that each E2F site mediates specific interactions with individual E2F family members. In addition, transient expression assays with mutagenized promoter constructs indicate that the functional role of each site is also dependent on its position relative to other regulatory elements in the promoter context. Thus, the two E2F sites play opposite genetic functions and control RanBP1 transcription through distinct molecular mechanisms.

Details

ISSN :
00219258
Volume :
274
Database :
OpenAIRE
Journal :
Journal of Biological Chemistry
Accession number :
edsair.doi.dedup.....262c38fdb1e17c5caf333a46c8815d1b
Full Text :
https://doi.org/10.1074/jbc.274.15.10339