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  1. 原著論文

Site-specific O-GlcNAcylation of Psme3 maintains mouse stem cell pluripotency by impairing P-body homeostasis

https://repo.qst.go.jp/records/84040
https://repo.qst.go.jp/records/84040
67f0470c-25f9-4cb4-a679-ea66209ae975
Item type 学術雑誌論文 / Journal Article(1)
公開日 2021-07-15
タイトル
タイトル Site-specific O-GlcNAcylation of Psme3 maintains mouse stem cell pluripotency by impairing P-body homeostasis
言語
言語 eng
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
アクセス権
アクセス権 metadata only access
アクセス権URI http://purl.org/coar/access_right/c_14cb
著者 Pecori, Federico

× Pecori, Federico

WEKO 1014966

Pecori, Federico

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Kondo , Nanako

× Kondo , Nanako

WEKO 1014967

Kondo , Nanako

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Chika Ogura

× Chika Ogura

WEKO 1014968

Chika Ogura

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Miura, Taichi

× Miura, Taichi

WEKO 1014969

Miura, Taichi

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Kume, Masahiko

× Kume, Masahiko

WEKO 1014970

Kume, Masahiko

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Minamijima, Youhei

× Minamijima, Youhei

WEKO 1014971

Minamijima, Youhei

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Kazuo Yamamoto

× Kazuo Yamamoto

WEKO 1014972

Kazuo Yamamoto

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Nishihara, Shoko

× Nishihara, Shoko

WEKO 1014973

Nishihara, Shoko

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Chika, Ogura

× Chika, Ogura

WEKO 1014974

en Chika, Ogura

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Taichi, Miura

× Taichi, Miura

WEKO 1014975

en Taichi, Miura

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Shoko, Nishihara

× Shoko, Nishihara

WEKO 1014976

en Shoko, Nishihara

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内容記述タイプ Abstract
内容記述 Mouse embryonic stem cell (ESC) pluripotency is tightly regulated by a complex network composed of extrinsic and intrinsic factors that allow proper organismal development. O-linked β-N-acetylglucosamine (O-GlcNAc) is the sole glycosylation mark found on cytoplasmic and nuclear proteins and plays a pivotal role in regulating fundamental cellular processes; however, its function in ESC pluripotency is still largely unexplored. Here, we identify O-GlcNAcylation of proteasome activator subunit 3 (Psme3) protein as a node of the ESC pluripotency network. Mechanistically, O-GlcNAc modification of serine 111 (S111) of Psme3 promotes degradation of Ddx6, which is essential for processing body (P-body) assembly, resulting in the maintenance of ESC pluripotent state. Conversely, loss of Psme3 S111 O-GlcNAcylation stabilizes Ddx6 and increases P-body levels, culminating in spontaneous exit of ESC from the pluripotent state. Our findings establish O-GlcNAcylation at S111 of Psme3 as a switch that regulates ESC pluripotency via control of P-body homeostasis.
書誌情報 Cell Reports

巻 36, 号 2, p. 109361, 発行日 2021-07
出版者
出版者 Cell
ISSN
収録物識別子タイプ ISSN
収録物識別子 2211-1247
DOI
識別子タイプ DOI
関連識別子 10.1016/j.celrep.2021.109361
関連サイト
識別子タイプ URI
関連識別子 https://www.cell.com/cell-reports/pdf/S2211-1247(21)00759-2.pdf
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