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PMID: 10555142 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A functional enhancer suppresses silencing of a transgene and prevents its localization close to centrometric heterochromatin.

Cell ·Vol. 99 ·No. 3 ·1999-10-29 ·Pages 259-69

Francastel C, Walters MC, Groudine M, Martin DI

Abstract

To explore the mechanism by which enhancers maintain gene expression, we have assessed the ability of an enhancer and derivative mutants to influence silencing and nuclear location of a transgene. Using site-specific recombination to place different constructs at the same integration sites, we find that disruption of core enhancer motifs impairs the enhancer's ability to suppress silencing. FISH analysis reveals that active transgenes linked to a functional enhancer localize away from centromeres. However, enhancer mutations that result in increased rates of transgene silencing fail to localize the transgene away from centromeric heterochromatin, even when the transgene is in an active state. These mutations thus dissociate transcriptional activity and subnuclear location. Together, our results suggest that the functional enhancer antagonizes gene silencing by preventing localization of a gene near centromeric heterochromatin.

MeSH Terms
Enhancer Elements, Genetic Gene Expression Regulation Genes, Reporter Globins/genetics Heterochromatin/genetics Humans In Situ Hybridization, Fluorescence K562 Cells Mutagenesis Promoter Regions, Genetic Recombinant Fusion Proteins/biosynthesis Restriction Mapping Transfection beta-Galactosidase/genetics
Chemicals
Heterochromatin Recombinant Fusion Proteins Globins beta-Galactosidase
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Francastel C
Fred Hutchinson Cancer Research Center, Seattle, Washington 98109, USA.
Walters M C
Groudine M
Martin D I
Article Info
Journal
Cell
Abbr.
Cell
ISSN
0092-8674
Published
1999-10-29
Pages
259-69
Language
English
Region
United States
NLM ID
0413066
Subset
IM
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