Lysine-specific histone demethylase 1 (LSD1) is a very recently discovered enzyme which specifically removes methyl groups from Lys4 of histone 3. We have addressed the functional properties of the protein demonstrating that histone demethylation involves the flavin-catalysed oxidation of the methylated lysine. The nature of the substrate that acts as the electron acceptor required to complete the catalytic cycle was investigated. LSD1 converts oxygen to hydrogen peroxide although this reactivity is not as pronounced as that of other flavin-dependent oxidases. Our findings raise the possibility that in vivo LSD1 might not necessarily function as an oxidase, but it might use alternative electron acceptors.

Histone Demethylation Catalysed by LSD1 is a Flavin-dependent Oxidative Process

FORNERIS, FEDERICO
Investigation
;
BINDA, CLAUDIA;MATTEVI, ANDREA;
2005-01-01

Abstract

Lysine-specific histone demethylase 1 (LSD1) is a very recently discovered enzyme which specifically removes methyl groups from Lys4 of histone 3. We have addressed the functional properties of the protein demonstrating that histone demethylation involves the flavin-catalysed oxidation of the methylated lysine. The nature of the substrate that acts as the electron acceptor required to complete the catalytic cycle was investigated. LSD1 converts oxygen to hydrogen peroxide although this reactivity is not as pronounced as that of other flavin-dependent oxidases. Our findings raise the possibility that in vivo LSD1 might not necessarily function as an oxidase, but it might use alternative electron acceptors.
2005
Molecular Biology & Genetics
Esperti anonimi
Inglese
Internazionale
STAMPA
579
2203
2207
5
Tematica Ex SIR: Istone demetilasi umana (Classif. Ex SIR:Articoli su riviste ISI )
chromatin; epigenetic; enzymology
5
info:eu-repo/semantics/article
262
Forneris, Federico; Binda, Claudia; Vanoni, Ma; Mattevi, Andrea; Battaglioli, E.
1 Contributo su Rivista::1.1 Articolo in rivista
none
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/134110
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