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YB-1、Puralpha和AP-1转录因子对人fas启动子的调控

Regulation of the human fas promoter by YB-1, Puralpha and AP-1 transcription factors.

作者信息

Lasham A, Lindridge E, Rudert F, Onrust R, Watson J

机构信息

Genesis Research and Development Corporation Limited, Auckland, New Zealand.

出版信息

Gene. 2000 Jul 11;252(1-2):1-13. doi: 10.1016/s0378-1119(00)00220-1.

DOI:10.1016/s0378-1119(00)00220-1
PMID:10903433
Abstract

Fas (CD95/Apo-1) gene expression is dysregulated in a number of diseased states. Towards understanding the regulation of fas gene expression, we previously identified activator and repressor elements within the human fas promoter. Using a combination of expression screening and reporter gene assays, we have identified transcription factors which bind to these elements and thereby regulate transcription of the fas promoter. These are three single-stranded DNA binding proteins, YB-1, Puralpha and Purbeta and two components of the AP-1 complex, c-Fos and c-Jun. c-Jun is a potent transcriptional activator of fas and stimulated expression levels up to 184-fold in reporter gene assays. Co-expression with c-Fos abrogated c-Jun-mediated activation. YB-1 and Puralpha are transcriptional repressors of fas and decreased basal transcription by 60-fold in reporter gene assays. Purbeta was predominantly an antagonist of YB-1/Puralpha-mediated repression. Overexpression of YB-1 and Puralpha in Jurkat cells was shown to reduce the level of cell surface Fas staining, providing further evidence that these proteins regulate the fas promoter. It has been suggested that YB-1 plays a role in cell proliferation as an activator of growth-associated gene expression. We have shown that YB-1 is a repressor of a cell death-associated gene fas. These results suggest that YB-1 may play an important role in controlling cell survival by co-ordinately regulating the expression of cell growth-associated and death-associated genes.

摘要

Fas(CD95/Apo-1)基因表达在多种疾病状态下失调。为了理解fas基因表达的调控机制,我们之前在人类fas启动子中鉴定出了激活子和抑制子元件。通过结合表达筛选和报告基因检测,我们鉴定出了与这些元件结合从而调控fas启动子转录的转录因子。它们是三种单链DNA结合蛋白YB-1、Puralpha和Purbeta以及AP-1复合物的两个组分c-Fos和c-Jun。c-Jun是fas的一种强效转录激活因子,在报告基因检测中可将表达水平提高至184倍。与c-Fos共表达可消除c-Jun介导的激活作用。YB-1和Puralpha是fas的转录抑制因子,在报告基因检测中可将基础转录水平降低60倍。Purbeta主要是YB-1/Puralpha介导的抑制作用的拮抗剂。在Jurkat细胞中过表达YB-1和Puralpha可降低细胞表面Fas染色水平,这进一步证明了这些蛋白对fas启动子的调控作用。有人提出YB-1作为生长相关基因表达的激活因子在细胞增殖中发挥作用。我们已经表明YB-1是细胞死亡相关基因fas的抑制因子。这些结果表明YB-1可能通过协调调控细胞生长相关基因和死亡相关基因的表达在控制细胞存活中发挥重要作用。

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