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PMID: 16408017 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Identification of a specific inhibitor of the histone methyltransferase SU(VAR)3-9.

Nature chemical biology ·Vol. 1 ·No. 3 ·2005-08-00 ·Pages 143-5

Greiner D, Bonaldi T, Eskeland R, Roemer E, Imhof A

Abstract

Histone methylation plays a key role in establishing and maintaining stable gene expression patterns during cellular differentiation and embryonic development. Here, we report the characterization of the fungal metabolite chaetocin as the first inhibitor of a lysine-specific histone methyltransferase. Chaetocin is specific for the methyltransferase SU(VAR)3-9 both in vitro and in vivo and may therefore be used to study heterochromatin-mediated gene repression.

MeSH Terms
Animals Drosophila Proteins/antagonists & inhibitors,genetics Histone Methyltransferases Histone-Lysine N-Methyltransferase/antagonists & inhibitors,classification Methyltransferases/antagonists & inhibitors Molecular Structure Mycotoxins/pharmacology Piperazines/pharmacology Poisons/pharmacology Protein Methyltransferases Recombinant Proteins/antagonists & inhibitors,genetics Substrate Specificity
Chemicals
Drosophila Proteins Mycotoxins Piperazines Poisons Recombinant Proteins chaetocin Histone Methyltransferases Methyltransferases Protein Methyltransferases SU(VAR)3-9 Histone-Lysine N-Methyltransferase
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Greiner Dorothea
Adolf Butenandt Institute, Department of Molecular Biology, Histone Modifications Group, Ludwig-Maximillians University of Munich, Schillerstr. 44, 80336 Munich, Germany.
Bonaldi Tiziana
Eskeland Ragnhild
Roemer Ernst
Imhof Axel
Article Info
Journal
Nature chemical biology
Abbr.
Nat Chem Biol
ISSN
1552-4450
Published
2005-08-00
Epub
2005-00-17
Pages
143-5
Language
English
Region
United States
NLM ID
101231976
Subset
IM
Databases
PubChem-Substance
866158
Corrections
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