Lysine-specific historic demethylase 1(LSD1) is a very recently discovered enzyme which specifically removes methyl groups from Lys4 of historic 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. (c) 2005 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.

Histone demethylation catalysed by LSD1 is a flavin-dependent oxidative process / F. Forneris, C. Binda, M.A. Vanoni, A. Mattevi, E. Battaglioli. - In: FEBS LETTERS. - ISSN 0014-5793. - 579:10(2005), pp. 2203-2207.

Histone demethylation catalysed by LSD1 is a flavin-dependent oxidative process

M.A. Vanoni;E. Battaglioli
Ultimo
2005

Abstract

Lysine-specific historic demethylase 1(LSD1) is a very recently discovered enzyme which specifically removes methyl groups from Lys4 of historic 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. (c) 2005 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
Amine oxidase; Chromatin remodelling; Flavoenzyme; Histone methylation; KIAA0601
Settore BIO/10 - Biochimica
Settore BIO/13 - Biologia Applicata
2005
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/5407
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