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  1. 原著論文

CHD1 acts via the Hmgpi pathway to regulate mouse early embryogenesis.

https://repo.qst.go.jp/records/47539
https://repo.qst.go.jp/records/47539
8ec05205-1703-4352-b65f-549d27a20519
Item type 学術雑誌論文 / Journal Article(1)
公開日 2016-09-05
タイトル
タイトル CHD1 acts via the Hmgpi pathway to regulate mouse early embryogenesis.
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 Suzuki, Shinnosuke

× Suzuki, Shinnosuke

WEKO 476406

Suzuki, Shinnosuke

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Nozawa, Yusuke

× Nozawa, Yusuke

WEKO 476407

Nozawa, Yusuke

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Tsukamoto, Satoshi

× Tsukamoto, Satoshi

WEKO 476408

Tsukamoto, Satoshi

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Kaneko, Takehito

× Kaneko, Takehito

WEKO 476409

Kaneko, Takehito

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Manabe, Ichiro

× Manabe, Ichiro

WEKO 476410

Manabe, Ichiro

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Imai, Hiroshi

× Imai, Hiroshi

WEKO 476411

Imai, Hiroshi

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Minami, Naojiro

× Minami, Naojiro

WEKO 476412

Minami, Naojiro

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塚本 智史

× 塚本 智史

WEKO 476413

en 塚本 智史

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抄録
内容記述タイプ Abstract
内容記述 The protein CHD1 is a member of the family of ATPase-dependent chromatin remodeling factors. CHD1, which recognizes trimethylated histone H3 lysine 4, has been implicated in transcriptional activation in organisms ranging from yeast to humans. It is required for pre-mRNA maturation, maintenance of mouse embryonic stem cell pluripotency and rapid growth of the mouse epiblast. However, the function(s) of CHD1 in mouse preimplantation embryos has not yet been examined. Here, we show that loss of CHD1 function led to embryonic lethality after implantation. In mouse embryos in which Chd1 was targeted by siRNA microinjection, the expression of the key regulators of cell fate specification Pou5f1 (also known as Oct4), Nanog and Cdx2 was dramatically decreased, starting at mid-preimplantation gene activation (MGA). Moreover, expression of Hmgpi and Klf5, which regulate Pou5f1, Nanog and Cdx2, was also significantly suppressed at zygotic gene activation (ZGA). Suppression of Hmgpi expression in Chd1-knockdown embryos continued until the blastocyst stage, whereas suppression of Klf5 expression was relieved by the morula stage. Next, we rescued HMGPI expression via Hmgpi mRNA microinjection in Chd1-knockdown embryos. Consequently, Pou5f1, Nanog and Cdx2 expression was restored at MGA and live offspring were recovered. These findings indicate that CHD1 plays important roles in mouse early embryogenesis via activation of Hmgpi at ZGA.
書誌情報 Development (Cambridge, England)

巻 142, 号 13, p. 2375-2384, 発行日 2015-07
出版者
出版者 Company Of Biologists Limited
ISSN
収録物識別子タイプ ISSN
収録物識別子 0950-1991
PubMed番号
識別子タイプ PMID
関連識別子 26092847
DOI
識別子タイプ DOI
関連識別子 10.1242/dev.120493
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