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静止和血清刺激的成纤维细胞中c-jun启动子处的体内蛋白质-DNA相互作用。

In vivo protein-DNA interactions at the c-jun promoter in quiescent and serum-stimulated fibroblasts.

作者信息

Rozek D, Pfeifer G P

机构信息

Department of Biology, Beckman Research Institute of the City of Hope, Duarte, California 91010, USA.

出版信息

J Cell Biochem. 1995 Mar;57(3):479-87. doi: 10.1002/jcb.240570313.

Abstract

c-Jun is an important component in the regulation of cell proliferation. As a member of the early response gene family, c-jun is induced within minutes in the presence of mitogenic agents such as serum growth factors. Using in vivo footprinting, we have analyzed protein-DNA interactions at the c-jun promoter in human fibroblasts subjected to growth arrest and serum stimulation. We located seven footprints upstream of the transcription initiation site. Protein-DNA interactions were detected at two AP-1-like sequences, A CCAAT box, an SP-1 sequence, an NF-jun sequence, a putative RSRF (related to serum response factor) binding site, and a sequence bound by an unknown factor. All of these binding sites were occupied in serum-starved cells, and no additional protein-DNA interactions were detected upon serum stimulation. Evidence from this study supports a model in which expression of the c-jun gene is mediated by phosphorylation events taking place on the transactivation domains of promoter-bound transcriptional activators.

摘要

c-Jun是细胞增殖调控中的一个重要组成部分。作为早期反应基因家族的一员,在有丝分裂原如血清生长因子存在的情况下,c-jun在数分钟内即可被诱导产生。我们利用体内足迹法,分析了处于生长停滞和血清刺激状态下的人成纤维细胞中c-jun启动子处的蛋白质-DNA相互作用。我们在转录起始位点上游定位到了七个足迹。在两个AP-1样序列、一个CCAAT盒、一个SP-1序列、一个NF-jun序列、一个假定的与血清反应因子相关的RSRF结合位点以及一个被未知因子结合的序列处检测到了蛋白质-DNA相互作用。所有这些结合位点在血清饥饿细胞中均被占据,血清刺激后未检测到额外的蛋白质-DNA相互作用。本研究的证据支持一种模型,即c-jun基因的表达是由启动子结合的转录激活因子的反式激活结构域上发生的磷酸化事件介导的。

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