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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

Human CYP2E1 is regulated by miR-378.

https://doi.org/10.24517/00015359
https://doi.org/10.24517/00015359
36eb78e4-275a-4b68-9d3f-421faced07bf
名前 / ファイル ライセンス アクション
PH-PR-NAKAJIMA-M-1045.pdf PH-PR-NAKAJIMA-M-1045.pdf (315.8 kB)
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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 Human CYP2E1 is regulated by miR-378.
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 10.24517/00015359
ID登録タイプ JaLC
著者 Mohri, Takuya

× Mohri, Takuya

WEKO 27924

Mohri, Takuya

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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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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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Takamiya, Masataka

× Takamiya, Masataka

WEKO 27925

Takamiya, Masataka

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Aoki, Yasuhiro

× Aoki, Yasuhiro

WEKO 27926

Aoki, Yasuhiro

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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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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 Biochemical pharmacology

巻 79, 号 7, p. 1045-1052, 発行日 2010-04-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0006-2952
NCID
収録物識別子タイプ NCID
収録物識別子 AA00564486
DOI
関連タイプ isVersionOf
識別子タイプ DOI
関連識別子 https://doi.org/10.1016/j.bcp.2009.11.015
出版者
出版者 Elsevier
抄録
内容記述タイプ Abstract
内容記述 Human CYP2E1 is one of the pharmacologically and toxicologically important cytochrome P450 isoforms. Earlier studies have reported that the CYP2E1 expression is extensively regulated by post-transcriptional and post-translational mechanisms, but the molecular basis remains unclear. In the present study, we examined the possibility that microRNA may be involved in the post-transcriptional regulation of human CYP2E1. In silico analysis identified a potential recognition element of miR-378 (MRE378) in the 3'-untranslated region (UTR) of human CYP2E1 mRNA. Luciferase assays using HEK293 cells revealed that the reporter activity of the plasmid containing the MRE378 was decreased by co-transfection of precursor miR-378, indicating that miR-378 functionally recognized the MRE378. We established two HEK293 cell lines stably expressing human CYP2E1 including or excluding 3'-UTR. When the precursor miR-378 was transfected into the cells expressing human CYP2E1 including 3'-UTR, the CYP2E1 protein level and chlorzoxazone 6-hydroxylase activity were significantly decreased, but were not in the cells expressing CYP2E1 excluding 3'-UTR. In both cell lines, the CYP2E1 mRNA levels were decreased by overexpression of miR-378, but miR-378 did not affect the stability of CYP2E1 mRNA. In a panel of 25 human livers, no positive correlation was observed between the CYP2E1 protein and CYP2E1 mRNA levels, supporting the post-transcriptional regulation. Interestingly, the miR-378 levels were inversely correlated with the CYP2E1 protein levels and the translational efficiency of CYP2E1. In conclusion, we found that human CYP2E1 expression is regulated by miR-378, mainly via translational repression. This study could provide new insight into the unsolved mechanism of the post-transcriptional regulation of CYP2E1. Copyright 2009 Elsevier Inc. All rights reserved.
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/00062952
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