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PMID: 11258701 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Chromosomal DNA demethylation specified by protein binding.

EMBO reports ·Vol. 2 ·No. 2 ·2001-02-00 ·Pages 108-12

Lin IG, Hsieh CL

Abstract

In the present study, we utilize the well-characterized Escherichia coli lac repressor/operator system to demonstrate that protein binding can lead to demethylation at the binding sites in the chromosome. Similar to the findings using the episome, we found that the presence of LacI in the cells can lead to demethylation of methylated lacO in the chromosome and the LacI inhibitor, isopropyl-beta-D-thiogalactopyranoside (IPTG), can prevent demethylation of the methylated lacO. The lacO sites become progressively more demethylated over time with the presence of LacI, supporting the role of protein occupancy in demethylation targeting. These results validate our earlier conclusions using a stable episomal system, and establish for the first time that protein binding can specify sites of demethylation in the chromosome.

MeSH Terms
Bacterial Proteins/genetics,metabolism Blotting, Southern Cell Line Chromosomes, Human/genetics,metabolism DNA Methylation/drug effects Escherichia coli/genetics Escherichia coli Proteins Genome, Human Humans Isopropyl Thiogalactoside/pharmacology Lac Operon/genetics Lac Repressors Protein Binding/drug effects Recombination, Genetic/genetics Repressor Proteins/genetics,metabolism Time Factors Transfection
Chemicals
Bacterial Proteins Escherichia coli Proteins Lac Repressors LacI protein, E coli Repressor Proteins Isopropyl Thiogalactoside
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Lin I G
Department of Urology, University of Southern California, Norris Cancer Center, Los Angeles 90033, USA.
Hsieh C L
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18 references, click to expand
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Article Info
Journal
EMBO reports
Abbr.
EMBO Rep
ISSN
1469-221X
Published
2001-02-00
Pages
108-12
Language
English
Region
England
NLM ID
100963049
PMCID
PMC1083819
Subset
IM
Grants
NIGMS NIH HHS · R01 GM054781 · United States
NIGMS NIH HHS · GM54781 · United States
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