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大鼠肝脏核蛋白与大鼠触珠蛋白基因细胞因子反应元件结合的急性期依赖性变化。

Acute phase-dependent changes in the binding of rat liver nucleoproteins to the cytokine response element of the rat haptoglobin gene.

作者信息

Sevaljević L J, Marinković-Pajović S, Grigorov I, Bogojević D, Ivanović-Matić S, Petrović M

机构信息

Institute for Biological Research, Belgrade, Yugoslavia.

出版信息

Int J Biochem Cell Biol. 1995 Feb;27(2):185-94. doi: 10.1016/1357-2725(94)00073-k.

Abstract

Hormones released during the acute phase reaction promote the transcriptional activation of the haptoglobin (Hp) gene and a consequent increase of Hp protein synthesis in the liver. The mechanisms underlying the alterations of basal transcription rates of eukaryotic genes are assumed to result from modulations of the binding affinities between nucleoproteins and specific DNA sequences in the enhancer and promoter elements. In order to characterize the changes in the interaction of nucleoproteins with the promoter that accompany the induction of the Hp gene, nuclear extracts from normal and inflamed livers were probed with hormone responsive element (HRE) of the rat Hp gene by gel mobility shift and Southwestern assays. Each of the three cis-acting sequences of the HRE, elements A, B, and C, recognized a distinct set of proteins. Together they conferred an additional level of specificity to the protein binding sites of the entire ABC-element. These sites were recognized by proteins in liver nuclear extracts isolated from both control and treated rats. The differences in the gel shift and Southwestern patterns of the corresponding DNA-protein complexes suggested that transcriptional activation of the Hp gene relied on changes in the concentrations and/or functional modifications of preexisting proteins rather than on the induction of new trans-acting factors.

摘要

急性期反应期间释放的激素促进触珠蛋白(Hp)基因的转录激活,并随之增加肝脏中Hp蛋白的合成。真核基因基础转录速率改变的潜在机制被认为是由于核蛋白与增强子和启动子元件中特定DNA序列之间结合亲和力的调节所致。为了表征伴随Hp基因诱导的核蛋白与启动子相互作用的变化,通过凝胶迁移率变动分析和蛋白质印迹法,用大鼠Hp基因的激素反应元件(HRE)对正常肝脏和炎症肝脏的核提取物进行检测。HRE的三个顺式作用序列(元件A、B和C)中的每一个都识别一组不同的蛋白质。它们共同为整个ABC元件的蛋白质结合位点赋予了额外的特异性水平。这些位点可被从对照大鼠和处理大鼠分离的肝脏核提取物中的蛋白质识别。相应DNA-蛋白质复合物的凝胶迁移率变动分析和蛋白质印迹模式的差异表明,Hp基因的转录激活依赖于现有蛋白质浓度的变化和/或功能修饰,而不是新的反式作用因子的诱导。

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