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  1. 原著論文

Histone methyltransferase Smyd3 regulates early embryonic lineage commitment in mice.

https://repo.qst.go.jp/records/47540
https://repo.qst.go.jp/records/47540
a6b59ccb-a13c-410d-a1d6-824b203835fe
Item type 学術雑誌論文 / Journal Article(1)
公開日 2016-09-06
タイトル
タイトル Histone methyltransferase Smyd3 regulates early embryonic lineage commitment in mice.
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 476414

Suzuki, Shinnosuke

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Nozawa, Yusuke

× Nozawa, Yusuke

WEKO 476415

Nozawa, Yusuke

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Tsukamoto, Satoshi

× Tsukamoto, Satoshi

WEKO 476416

Tsukamoto, Satoshi

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Kaneko, Takehito

× Kaneko, Takehito

WEKO 476417

Kaneko, Takehito

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Imai, Hiroshi

× Imai, Hiroshi

WEKO 476418

Imai, Hiroshi

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Minami, Naojiro

× Minami, Naojiro

WEKO 476419

Minami, Naojiro

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塚本 智史

× 塚本 智史

WEKO 476420

en 塚本 智史

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抄録
内容記述タイプ Abstract
内容記述 SET and MYND domain-containing protein 3 (Smyd3) is a histone H3 lysine 4 (H3K4) di- and tri-methyltransferase that forms a transcriptional complex with RNA polymerase II and activates the transcription of oncogenes and cell cycle genes in human cancer cells. However, the study of Smyd3 in mammalian early embryonic development has not yet been addressed. In the present study, we investigated the expression pattern of Smyd3 in mouse preimplantation embryos and the effects of RNA interference (RNAi)-mediated Smyd3 repression on the development of mouse embryos. We showed that Smyd3 mRNA levels increased after the two-cell stage, peaked at the four-cell stage, and gradually decreased thereafter. Moreover, in two-cell to eight-cell embryos, SMYD3 staining was more intense in the nuclei than it was in the cytoplasm. In Smyd3-knockdown embryos, the percentage of inner cell mass (ICM)-derived colony formation and trophectoderm (TE)-derived cell attachment were significantly decreased, which resulted in a reduction in the number of viable offspring. Furthermore, the expression of Oct4 and Cdx2 during mid-preimplantation gene activation was significantly decreased in Smyd3-knockdown embryos. In addition, the transcription levels of ICM and epiblast markers, such as Oct4, Nanog, and Sox2, the transcription levels of primitive endoderm markers, such as Gata6, and the transcription levels of TE markers, such as Cdx2 and Eomes, were significantly decreased in Smyd3-knockdown blastocysts. These findings indicate that SMYD3 plays an important role in early embryonic lineage commitment and peri-implantation development through the activation of lineage-specific genes.
書誌情報 Reproduction (Cambridge, England)

巻 150, 号 1, p. 21-30, 発行日 2015-07
出版者
出版者 Published for the Society for Reproduction and Fertility by BioScientifica
ISSN
収録物識別子タイプ ISSN
収録物識別子 1470-1626
PubMed番号
識別子タイプ PMID
関連識別子 25918436
DOI
識別子タイプ DOI
関連識別子 10.1530/REP-15-0019
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