Suppr超能文献

调控脂肪细胞分化中基因表达的核蛋白复合物:c-fos的直接参与。

Nucleoprotein complexes that regulate gene expression in adipocyte differentiation: direct participation of c-fos.

作者信息

Distel R J, Ro H S, Rosen B S, Groves D L, Spiegelman B M

出版信息

Cell. 1987 Jun 19;49(6):835-44. doi: 10.1016/0092-8674(87)90621-0.

Abstract

Adipocyte differentiation is accompanied by the transcriptional activation of many new genes, including a putative lipid-binding protein termed adipocyte P2 (aP2). The aP2 gene contains a regulatory element (FSE2) 124 bases 5' to its start of transcription. This element binds nuclear factors in sequence-specific and differentiation-dependent fashion as determined by altered mobility in gel retardation assays. Deletion analysis of promoter-linked transfection assays and competition of these constructions in cells with a synthetic FSE2 element suggest that trans-acting factors bind to this region and act as negative regulators of aP2 gene activity in preadipocytes. c-fos appears to participate directly in this nucleoprotein complex, as demonstrated by the ability of antibodies to c-fos to disrupt specific binding of factors to the FSE2 sequence but not to factor-binding sequences from several other genes. Antibodies to c-fos specifically immunoprecipitate protein complexes covalently bound to FSE2 DNA via UV cross-linking.

摘要

脂肪细胞分化伴随着许多新基因的转录激活,包括一种被称为脂肪细胞P2(aP2)的假定脂质结合蛋白。aP2基因在其转录起始点上游124个碱基处含有一个调控元件(FSE2)。通过凝胶阻滞试验中迁移率的改变确定,该元件以序列特异性和分化依赖性方式结合核因子。启动子连接的转染试验的缺失分析以及这些构建体在细胞中与合成FSE2元件的竞争表明,反式作用因子结合到该区域并作为前脂肪细胞中aP2基因活性的负调节因子。c-fos似乎直接参与了这种核蛋白复合物,这是通过抗c-fos抗体破坏因子与FSE2序列的特异性结合但不破坏来自其他几个基因的因子结合序列的能力来证明的。抗c-fos抗体通过紫外线交联特异性免疫沉淀与FSE2 DNA共价结合的蛋白复合物。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验