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在人bcl-2基因3'非翻译区鉴定功能性过氧化物酶体增殖物激活受体反应元件。

Identification of a functional peroxisome proliferator activated receptor response element in the 3' untranslated region of the human bcl-2 gene.

作者信息

Butts Brent D, Tran Nhan L, Briehl Margaret M

机构信息

Department of Pharmacology, University of Colorado, VAMC, Denver, CO 80220, USA.

出版信息

Int J Oncol. 2004 May;24(5):1305-10.

Abstract

Peroxisome proliferator activated receptors are nuclear hormone receptors that regulate the expression of genes containing a peroxisome proliferator activated receptor response element. We report here that the human bcl-2 gene contains a functional peroxisome proliferator activated receptor response element in the 3' untranslated region. Peroxisome proliferator activated receptor gamma bound the human bcl-2 peroxisome proliferator activated receptor response element in gel shift assays and co-transfection of this receptor led to increased luciferase activity from a reporter plasmid containing the human bcl-2 peroxisome proliferator activated receptor response element. Examination of peroxisome proliferator activated receptor gamma-transfected cells demonstrated an increased amount of bcl-2 message compared to empty vector-transfected cells. Confocal analyses confirmed that more Bcl-2 protein was present in peroxisome proliferator activated receptor gamma-transfected cells compared to control-transfected cells. The functionality of the increased Bcl-2 protein was examined using resistance to bile salt-induced apoptosis as the endpoint. Peroxisome proliferator activated receptor gamma-transfected cells were almost twice as resistant as control-transfected cells. These data show that PPARgamma can mediate transcription of bcl-2, resulting in an increase in Bcl-2 protein and protection from apoptosis. We discuss these findings with regards to their potential implications for colon carcinogenesis.

摘要

过氧化物酶体增殖物激活受体是核激素受体,可调节含有过氧化物酶体增殖物激活受体反应元件的基因的表达。我们在此报告,人类bcl-2基因在3'非翻译区含有一个功能性过氧化物酶体增殖物激活受体反应元件。在凝胶迁移试验中,过氧化物酶体增殖物激活受体γ与人类bcl-2过氧化物酶体增殖物激活受体反应元件结合,该受体的共转染导致含有人类bcl-2过氧化物酶体增殖物激活受体反应元件的报告质粒的荧光素酶活性增加。与空载体转染细胞相比,对过氧化物酶体增殖物激活受体γ转染细胞的检测显示bcl-2信使核糖核酸的量增加。共聚焦分析证实,与对照转染细胞相比,过氧化物酶体增殖物激活受体γ转染细胞中存在更多的Bcl-2蛋白。以对胆盐诱导的凋亡的抗性为终点,检测增加的Bcl-2蛋白的功能。过氧化物酶体增殖物激活受体γ转染细胞的抗性几乎是对照转染细胞的两倍。这些数据表明,PPARγ可介导bcl-2的转录,导致Bcl-2蛋白增加并保护细胞免受凋亡。我们讨论了这些发现对结肠癌发生的潜在影响。

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