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

被引:231
作者
Forneris, F
Binda, C
Vanoni, MA
Mattevi, A
Battaglioli, E
机构
[1] Univ Pavia, Dipartimento Genet & Microbiol, I-27100 Pavia, Italy
[2] Univ Milan, Dipartimento Sci Biomol & Biotecnol, I-20133 Milan, Italy
[3] Univ Milan, Dipartimento Biol & Genet Sci Med, I-20133 Milan, Italy
关键词
flavoenzyme; amine oxidase; KIAA0601; historic methylation; chromatin remodelling;
D O I
10.1016/j.febslet.2005.03.015
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:2203 / 2207
页数:5
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