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PMID: 15053881 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Polycomb silencing blocks transcription initiation.

Molecular cell ·Vol. 13 ·No. 6 ·2004-03-26 ·Pages 887-93

Dellino GI, Schwartz YB, Farkas G, McCabe D, Elgin SC, Pirrotta V

Abstract

Polycomb (PcG) complexes maintain the silent state of target genes. The mechanism of silencing is not known but has been inferred to involve chromatin packaging to block the access of transcription factors. We have studied the effect of PcG silencing on the hsp26 heat shock promoter. While silencing does decrease the accessibility of some restriction enzyme sites to some extent, it does not prevent the binding of TBP, RNA polymerase, or the heat shock factor to the hsp26 promoter, as shown by chromatin immunoprecipitation. However, we find that in the repressed state, the RNA polymerase cannot initiate transcription. We conclude that, rather than altering chromatin structure to block accessibility, PcG silencing in this construct targets directly the activity of the transcriptional machinery at the promoter.

MeSH Terms
Animals Biomarkers Chromatin/metabolism DNA Footprinting DNA Transposable Elements DNA-Directed RNA Polymerases/metabolism Drosophila Drosophila Proteins/genetics,metabolism Gene Silencing Genes, Insect Heat-Shock Proteins/genetics Polycomb Repressive Complex 1 Precipitin Tests Promoter Regions, Genetic Transcription Factors/metabolism Transcription, Genetic Transgenes
Chemicals
Biomarkers Chromatin DNA Transposable Elements Drosophila Proteins Heat-Shock Proteins Pc protein, Drosophila Transcription Factors Polycomb Repressive Complex 1 DNA-Directed RNA Polymerases
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Dellino Gaetano I
Department of Zoology, University of Geneva, 30 quai Ernest Ansermet, CH-1211 Geneva, Switzerland.
Schwartz Yuri B
Farkas Gabriella
McCabe Donna
Elgin Sarah C R
Pirrotta Vincenzo
Article Info
Journal
Molecular cell
Abbr.
Mol Cell
ISSN
1097-2765
Published
2004-03-26
Pages
887-93
Language
English
Region
United States
NLM ID
9802571
Subset
IM
Grants
NIGMS NIH HHS · GM 31532 · United States
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