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利用选择性诱导系统鉴定Fos靶基因。

Identification of Fos target genes by the use of selective induction systems.

作者信息

Braselmann S, Bergers G, Wrighton C, Graninger P, Superti-Furga G, Busslinger M

机构信息

Institute of Molecular Pathology, Vienna, Austria.

出版信息

J Cell Sci Suppl. 1992;16:97-109. doi: 10.1242/jcs.1992.supplement_16.12.

Abstract

c-Fos is a major component of the transcription factor AP-1 which has been implicated in the control of cell proliferation and differentiation as well as in transformation. In order to identify Fos target genes involved in these processes, we have taken advantage of the regulatory properties of the hormone-binding domain of the human estrogen receptor to develop transcriptional and post-translational induction systems, both of which allow selective elevation of Fos activity within a cell. Using this approach we have searched for Fos-responsive genes in rat fibroblasts and PC12 cells. Here we describe the identification and regulation of five Fos-responsive genes encoding a transcription factor (Fra-1), a secreted protein (Fit-1), a biosynthetic enzyme (ODC) and two membrane-associated proteins (annexin II and V), respectively. The post-translational induction system was also used to study the Fos-mediated block of neuronal differentiation of PC12 cells. These experiments demonstrate that Fos activity is dominant over NGF function and interferes with the expression of late NGF-inducible genes.

摘要

c-Fos是转录因子AP-1的主要组成部分,AP-1与细胞增殖、分化以及转化的调控有关。为了鉴定参与这些过程的Fos靶基因,我们利用人雌激素受体激素结合域的调控特性开发了转录和翻译后诱导系统,这两种系统都能使细胞内Fos活性选择性升高。利用这种方法,我们在大鼠成纤维细胞和PC12细胞中寻找Fos反应性基因。在此,我们描述了分别编码一种转录因子(Fra-1)、一种分泌蛋白(Fit-1)、一种生物合成酶(ODC)和两种膜相关蛋白(膜联蛋白II和V)的五个Fos反应性基因的鉴定和调控。翻译后诱导系统还用于研究Fos介导的PC12细胞神经元分化阻滞。这些实验表明,Fos活性比NGF功能占优势,并干扰晚期NGF诱导基因的表达。

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