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Nucleosome Binding by the Lysine Specific Demethylase 1 (LSD1) Enzyme Enables Histone H3 Demethylation.

Authors :
Dhall A
Shelton PMM
Delachat AM
Leonen CJA
Fierz B
Chatterjee C
Source :
Biochemistry [Biochemistry] 2020 Jul 14; Vol. 59 (27), pp. 2479-2483. Date of Electronic Publication: 2020 Jun 26.
Publication Year :
2020

Abstract

The essential human enzyme lysine specific demethylase 1 (LSD1) silences genes by demethylating mono- and dimethylated lysine 4 in histone H3 (H3K4me1/2). Studies of the minimal requirements for LSD1 activity are complicated by the heterogeneity of histone modification states in cells. We overcame this challenge by generating homogeneous mononucleosome substrates containing semisynthetic H3K4me2. Biophysical and biochemical assays with full-length LSD1 revealed its ability to bind and demethylate nucleosomes. Consistent with a requirement for nucleosome binding prior to demethylation, a competing nucleosome-binding peptide from the high-mobility group protein effectively inhibited LSD1 activity. Thus, our studies provide the first glimpse of nucleosome demethylation by LSD1 in the absence of other scaffolding proteins.

Details

Language :
English
ISSN :
1520-4995
Volume :
59
Issue :
27
Database :
MEDLINE
Journal :
Biochemistry
Publication Type :
Academic Journal
Accession number :
32567837
Full Text :
https://doi.org/10.1021/acs.biochem.0c00412