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Novel O-GlcNAcylation on Ser(40) of canonical H2A isoforms specific to viviparity

We report here newly discovered O-linked-N-acetylglucosamine (O-GlcNAc) modification of histone H2A at Ser(40) (H2AS40Gc). The mouse genome contains 18 H2A isoforms, of which 13 have Ser(40) and the other five have Ala(40). The combination of production of monoclonal antibody and mass spectrometric...

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Autores principales: Hirosawa, Mitsuko, Hayakawa, Koji, Yoneda, Chikako, Arai, Daisuke, Shiota, Hitoshi, Suzuki, Takehiro, Tanaka, Satoshi, Dohmae, Naoshi, Shiota, Kunio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018834/
https://www.ncbi.nlm.nih.gov/pubmed/27615797
http://dx.doi.org/10.1038/srep31785
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author Hirosawa, Mitsuko
Hayakawa, Koji
Yoneda, Chikako
Arai, Daisuke
Shiota, Hitoshi
Suzuki, Takehiro
Tanaka, Satoshi
Dohmae, Naoshi
Shiota, Kunio
author_facet Hirosawa, Mitsuko
Hayakawa, Koji
Yoneda, Chikako
Arai, Daisuke
Shiota, Hitoshi
Suzuki, Takehiro
Tanaka, Satoshi
Dohmae, Naoshi
Shiota, Kunio
author_sort Hirosawa, Mitsuko
collection PubMed
description We report here newly discovered O-linked-N-acetylglucosamine (O-GlcNAc) modification of histone H2A at Ser(40) (H2AS40Gc). The mouse genome contains 18 H2A isoforms, of which 13 have Ser(40) and the other five have Ala(40). The combination of production of monoclonal antibody and mass spectrometric analyses with reverse-phase (RP)-high performance liquid chromatography (HPLC) fractionation indicated that the O-GlcNAcylation is specific to the Ser(40) isoforms. The H2AS40Gc site is in the L1 loop structure where two H2A molecules interact in the nucleosome. Targets of H2AS40Gc are distributed genome-wide and are dramatically changed during the process of differentiation in mouse trophoblast stem cells. In addition to the mouse, H2AS40Gc was also detected in humans, macaques and cows, whereas non-mammalian species possessing only the Ala(40) isoforms, such as silkworms, zebrafish and Xenopus showed no signal. Genome database surveys revealed that Ser(40) isoforms of H2A emerged in Marsupialia and persisted thereafter in mammals. We propose that the emergence of H2A Ser(40) and its O-GlcNAcylation linked a genetic event to genome-wide epigenetic events that correlate with the evolution of placental animals.
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spelling pubmed-50188342016-09-19 Novel O-GlcNAcylation on Ser(40) of canonical H2A isoforms specific to viviparity Hirosawa, Mitsuko Hayakawa, Koji Yoneda, Chikako Arai, Daisuke Shiota, Hitoshi Suzuki, Takehiro Tanaka, Satoshi Dohmae, Naoshi Shiota, Kunio Sci Rep Article We report here newly discovered O-linked-N-acetylglucosamine (O-GlcNAc) modification of histone H2A at Ser(40) (H2AS40Gc). The mouse genome contains 18 H2A isoforms, of which 13 have Ser(40) and the other five have Ala(40). The combination of production of monoclonal antibody and mass spectrometric analyses with reverse-phase (RP)-high performance liquid chromatography (HPLC) fractionation indicated that the O-GlcNAcylation is specific to the Ser(40) isoforms. The H2AS40Gc site is in the L1 loop structure where two H2A molecules interact in the nucleosome. Targets of H2AS40Gc are distributed genome-wide and are dramatically changed during the process of differentiation in mouse trophoblast stem cells. In addition to the mouse, H2AS40Gc was also detected in humans, macaques and cows, whereas non-mammalian species possessing only the Ala(40) isoforms, such as silkworms, zebrafish and Xenopus showed no signal. Genome database surveys revealed that Ser(40) isoforms of H2A emerged in Marsupialia and persisted thereafter in mammals. We propose that the emergence of H2A Ser(40) and its O-GlcNAcylation linked a genetic event to genome-wide epigenetic events that correlate with the evolution of placental animals. Nature Publishing Group 2016-09-12 /pmc/articles/PMC5018834/ /pubmed/27615797 http://dx.doi.org/10.1038/srep31785 Text en Copyright © 2016, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Hirosawa, Mitsuko
Hayakawa, Koji
Yoneda, Chikako
Arai, Daisuke
Shiota, Hitoshi
Suzuki, Takehiro
Tanaka, Satoshi
Dohmae, Naoshi
Shiota, Kunio
Novel O-GlcNAcylation on Ser(40) of canonical H2A isoforms specific to viviparity
title Novel O-GlcNAcylation on Ser(40) of canonical H2A isoforms specific to viviparity
title_full Novel O-GlcNAcylation on Ser(40) of canonical H2A isoforms specific to viviparity
title_fullStr Novel O-GlcNAcylation on Ser(40) of canonical H2A isoforms specific to viviparity
title_full_unstemmed Novel O-GlcNAcylation on Ser(40) of canonical H2A isoforms specific to viviparity
title_short Novel O-GlcNAcylation on Ser(40) of canonical H2A isoforms specific to viviparity
title_sort novel o-glcnacylation on ser(40) of canonical h2a isoforms specific to viviparity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018834/
https://www.ncbi.nlm.nih.gov/pubmed/27615797
http://dx.doi.org/10.1038/srep31785
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