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SIRT2 Reverses 4-Oxononanoyl Lysine Modification on Histones.

ABSTRACT: Post-translational modifications (PTMs) regulate numerous proteins and are important for many biological processes. Lysine 4-oxononanoylation (4-ONylation) is a newly discovered histone PTM that prevents nucleosome assembly under oxidative stress. Whether there are cellular enzymes that remove 4-ONyl from histones remains unknown, which hampers the further investigation of the cellular function of this PTM. Here, we report that mammalian SIRT2 can remove 4-ONyl from histones and other proteins in live cells. A crystal structure of SIRT2 in complex with a 4-ONyl peptide reveals a lone pair-? interaction between Phe119 and the ketone oxygen of the 4-ONyl group. This is the first time that a mechanism to reverse 4-ONyl lysine modification is reported and will help to understand the role of SIRT2 in oxidative stress responses and the function of 4-ONylation.

SUBMITTER: Jin J

PROVIDER: S-EPMC5305808 | biostudies-literature | 2016 Sep

REPOSITORIES: biostudies-literature

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SIRT2 Reverses 4-Oxononanoyl Lysine Modification on Histones.

Jin Jing J He Bin B Zhang Xiaoyu X Lin Hening H Wang Yi Y

Journal of the American Chemical Society 20160915 38

Post-translational modifications (PTMs) regulate numerous proteins and are important for many biological processes. Lysine 4-oxononanoylation (4-ONylation) is a newly discovered histone PTM that prevents nucleosome assembly under oxidative stress. Whether there are cellular enzymes that remove 4-ONyl from histones remains unknown, which hampers the further investigation of the cellular function of this PTM. Here, we report that mammalian SIRT2 can remove 4-ONyl from histones and other proteins i ...[more]

PMID: 27610633

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