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  1. C. 医薬保健学域; 医学類・薬学類・医薬科学類・保健学類
  2. c 10. 学術雑誌掲載論文(医・保健)
  3. 1. 査読済論文(医学・保健)

ETS-related transcription factors Etv4 and Etv5 are involved in proliferation and induction of differentiationassociated genes in embryonic stem (ES) cells

http://hdl.handle.net/2297/43423
http://hdl.handle.net/2297/43423
5d2c8df3-d438-44f1-a178-4f699a3168d4
名前 / ファイル ライセンス アクション
ME-PR-AKAGI-T-22460.pdf ME-PR-AKAGI-T-22460.pdf (1.9 MB)
Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-03
タイトル
タイトル ETS-related transcription factors Etv4 and Etv5 are involved in proliferation and induction of differentiationassociated genes in embryonic stem (ES) cells
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
著者 Akagi, Tadayuki

× Akagi, Tadayuki

WEKO 490
金沢大学研究者情報 70532183
研究者番号 70532183

Akagi, Tadayuki

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Kuure, Satu

× Kuure, Satu

WEKO 24248

Kuure, Satu

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Uranishi, Kousuke

× Uranishi, Kousuke

WEKO 24249

Uranishi, Kousuke

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Koide, Hiroshi

× Koide, Hiroshi

WEKO 84
e-Rad 70260536
研究者番号 70260536

Koide, Hiroshi

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Costantini, Frank

× Costantini, Frank

WEKO 24250

Costantini, Frank

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Yokota, Takashi

× Yokota, Takashi

WEKO 41
e-Rad 50134622
金沢大学研究者情報 50134622
研究者番号 50134622

Yokota, Takashi

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書誌情報 Journal of Biological Chemistry

巻 290, 号 37, p. 22460-22473, 発行日 2015-09-11
ISSN
収録物識別子タイプ ISSN
収録物識別子 0021-9258
NCID
収録物識別子タイプ NCID
収録物識別子 AA00251083
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 10.1074/jbc.M115.675595
出版者
出版者 American Society for Biochemistry and Molecular Biology Inc.
抄録
内容記述タイプ Abstract
内容記述 The pluripotency and self-renewal capacity of embryonic stem (ES) cells is regulated by several transcription factors. Here, we show that the ETS-related transcription factors Etv4 and Etv5 (Etv4/5) are specifically expressed in undifferentiated ES cells, and suppression of Oct3/4 results in down-regulation of Etv4/5. Simultaneous deletion of Etv4 and Etv5 (Etv4/5 double knock-out(dKO)) in ES cells resulted in a flat, epithelial cell-like appearance, whereas the morphology changed into compact colonies in a 2i medium (containing two inhibitors for GSK3 and MEK/ERK). Expression levels of self-renewal marker genes, including Oct3/4 and Nanog, were similar between wild-type and dKO ES cells, whereas proliferation of Etv4/5 dKO ES cells was decreased with overexpression of cyclin-dependent kinase inhibitors (p16/p19, p15, and p57). A differentiation assay revealed that the embryoid bodies derived from Etv4/5 dKO ES cells were smaller than the control, and expression of ectoderm marker genes, including Fgf5, Sox1, and Pax3, was not induced in dKO-derived embryoid bodies. Microarray analysis demonstrated that stem cell-related genes, including Tcf15, Gbx2, Lrh1, Zic3, and Baf60c, were significantly repressed in Etv4/5dKOEScells.Theartificial expression of Etv4 and/or Etv5 in Etv4/5 dKO ES cells induced re-expression of Tcf15 and Gbx2. These results indicate that Etv4 and Etv5, potentially through regulation of Gbx2 and Tcf15, are involved in the ES cell proliferation and induction of differentiation-associated genes in ES cells. © 2015 by The American Society for Biochemistry and Molecular Biology, Inc. Published in the U.S.A.
著者版フラグ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
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