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  1. H-2. ナノ生命科学研究所
  2. h-2 10.学術雑誌掲載論文
  3. 1. 査読済論文

Aryl hydrocarbon receptor nuclear translocator in human liver is regulated by miR-24

https://doi.org/10.24517/00014983
https://doi.org/10.24517/00014983
6b6152e6-28ce-4f3c-a9ab-83de2cfdcbef
名前 / ファイル ライセンス アクション
PH-PR-NAKAJIMA-M-222.pdf PH-PR-NAKAJIMA-M-222.pdf (2.5 MB)
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Item type 学術雑誌論文 / Journal Article(1)
公開日 2017-10-04
タイトル
タイトル Aryl hydrocarbon receptor nuclear translocator in human liver is regulated by miR-24
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
ID登録
ID登録 10.24517/00014983
ID登録タイプ JaLC
著者 Oda, Yuki

× Oda, Yuki

WEKO 26958

Oda, Yuki

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Nakajima, Miki

× Nakajima, Miki

WEKO 196
e-Rad 70266162
金沢大学研究者情報 70266162
研究者番号 70266162

Nakajima, Miki

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Mohri, Takuya

× Mohri, Takuya

WEKO 26959

Mohri, Takuya

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Takamiya, Masataka

× Takamiya, Masataka

WEKO 26960

Takamiya, Masataka

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Aoki, Yasuhiro

× Aoki, Yasuhiro

WEKO 26961

Aoki, Yasuhiro

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Fukami, Tatsuki

× Fukami, Tatsuki

WEKO 26716
e-Rad 00532300
金沢大学研究者情報 00532300
研究者番号 00532300

Fukami, Tatsuki

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Yokoi, Tsuyoshi

× Yokoi, Tsuyoshi

WEKO 63
研究者番号 70135226

Yokoi, Tsuyoshi

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著者別表示 中嶋, 美紀

× 中嶋, 美紀

中嶋, 美紀

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深見, 達基

× 深見, 達基

深見, 達基

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横井, 毅

× 横井, 毅

横井, 毅

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提供者所属
内容記述タイプ Other
内容記述 金沢大学ナノ生命科学研究所 / 金沢大学医薬保健研究域薬学系
書誌情報 Toxicology and Applied Pharmacology

巻 260, 号 3, p. 222-231, 発行日 2012-05-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0041-008X
NCID
収録物識別子タイプ NCID
収録物識別子 AA00864435
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 10.1016/j.taap.2012.02.012
出版者
出版者 Elsevier
抄録
内容記述タイプ Abstract
内容記述 Aryl hydrocarbon receptor nuclear translocator (ARNT) forms a heterodimer with aryl hydrocarbon receptor or hypoxia inducible factor 1α to mediate biological responses to xenobiotic exposure and hypoxia. Although the regulation mechanism of the ARNT expression is largely unknown, earlier studies reported that the human ARNT protein level was decreased by hydrogen peroxide or reactive oxygen species. These stimuli increase the miR-24 level in various human cell lines. In silico analysis predicts that some microRNAs including miR-16 and miR-23b may bind to ARNT mRNA. This background prompted us to investigate whether human ARNT is regulated by microRNAs. Overexpression of miR-24 into HuH-7 and HepG2 cells significantly decreased the ARNT protein level, but not the ARNT mRNA level, indicating translational repression. However, overexpression of miR-16 or miR-23b caused no change in the ARNT expression. The miR-24-dependent down-regulation of ARNT decreased the expression of its downstream genes such as CYP1A1 and carbonic anhydrase IX. Luciferase assay was performed to determine the element on the ARNT mRNA to which miR-24 binds. Finally, it was demonstrated that the miR-24 levels in a panel of 26 human livers were inversely correlated with the protein levels or the translational efficiency of ARNT. Taken together, we found that miR-24 negatively regulates ARNT expression in human liver, affecting the expression of its downstream genes. miR-24 would be one of the factors underlying the mechanisms by which ARNT protein is decreased by reactive oxygen species. © 2012 Elsevier Inc.
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
関連URI
識別子タイプ URI
関連識別子 http://www.elsevier.com/locate/issn/0041008X
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