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PMID: 11726539 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

DNA methylation-dependent chromatin fiber compaction in vivo and in vitro: requirement for linker histone.

Karymov MA, Tomschik M, Leuba SH, Caiafa P, Zlatanova J

Abstract

Dynamic alterations in chromatin structure mediated by postsynthetic histone modifications and DNA methylation constitute a major regulatory mechanism in DNA functioning. DNA methylation has been implicated in transcriptional silencing, in part by inducing chromatin condensation. To understand the methylation-dependent chromatin structure, we performed atomic force microscope (AFM) studies of fibers isolated from cultured cells containing normal or elevated levels of m5C. Chromatin fibers were reconstituted on control or methylated DNA templates in the presence or absence of linker histone. Visual inspection of AFM images, combined with quantitative analysis of fiber structural parameters, suggested that DNA methylation induced fiber compaction only in the presence of linker histones. This conclusion was further substantiated by biochemical results.

MeSH Terms
3T3 Cells Animals Base Sequence Centrifugation, Density Gradient Chromatin/chemistry,metabolism,ultrastructure Cytosine/metabolism DNA/genetics,metabolism DNA Methylation Histones/chemistry,metabolism Mice Microscopy, Atomic Force Molecular Sequence Data Nucleosomes/chemistry,metabolism,ultrastructure Templates, Genetic
Chemicals
Chromatin Histones Nucleosomes Cytosine DNA
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Karymov M A
Physical Molecular Biology, Laboratory of Receptor Biology and Gene Expression, National Cancer Institute, National Institutes of Health, Bethesda, Maryland 20892-5055, USA.
Tomschik M
Leuba S H
Caiafa P
Zlatanova J
Article Info
Journal
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
Abbr.
FASEB J
ISSN
1530-6860
Published
2001-12-00
Pages
2631-41
Language
English
Region
United States
NLM ID
8804484
Subset
IM
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