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在人类Aγ-珠蛋白基因5'-非翻译区内鉴定出两个新型调控元件。

Identification of two novel regulatory elements within the 5'-untranslated region of the human A gamma-globin gene.

作者信息

Amrolia P J, Cunningham J M, Ney P, Nienhuis A W, Jane S M

机构信息

Division of Experimental Hematology, St. Jude Children's Research Hospital, Memphis, Tennessee 38101, USA.

出版信息

J Biol Chem. 1995 May 26;270(21):12892-8. doi: 10.1074/jbc.270.21.12892.

Abstract

Interaction between the stage selector element (SSE) in the proximal gamma-globin promoter and hypersensitivity site 2 in the locus control region partly mediates the competitive silencing of the beta-globin promoter in the fetal developmental stage. We have now demonstrated that a second SSE-like element in the 5'-untranslated region of the gamma-gene also contributes to this competitive silencing of the beta-gene. Utilizing transient transfection assays in the fetal erythroid cell line, K562, we have shown that the core enhancer of hypersensitivity site 2 can preferentially interact with the proximal gamma-promoter in the absence of the SSE, completely silencing a linked beta-promoter. Mutation of a 20-base pair sequence of the gamma-gene 5'-untranslated region (UTR) led to derepression of beta-promoter activity. A marked activation of gamma-promoter activity was also observed with this mutation, suggesting the presence of a repressor. Fine mutagenesis dissected these activities to different regions of the 5'-UTR. The stage selector activity was localized to a region centered on nucleotides +13 to +15. Electromobility shift assays utilizing this sequence demonstrated binding of a fetal and erythroid-specific protein. The repressor activity of the 5'-UTR was localized to tandem GATA-like sites, which appear to bind a complex of two proteins, one of which is the erythroid transcription factor GATA-1. These results indicate that the 5'-UTR of the gamma-gene contains sequences that may be important for its transcriptional and developmental regulation.

摘要

近端γ-珠蛋白启动子中的阶段选择元件(SSE)与基因座控制区的超敏位点2之间的相互作用,部分介导了胎儿发育阶段β-珠蛋白启动子的竞争性沉默。我们现已证明,γ基因5'非翻译区中的第二个SSE样元件也促成了β基因的这种竞争性沉默。利用胎儿红系细胞系K562中的瞬时转染试验,我们发现,在没有SSE的情况下,超敏位点2的核心增强子可优先与近端γ启动子相互作用,从而完全沉默与之相连的β启动子。γ基因5'非翻译区(UTR)的一个20碱基对序列发生突变,导致β启动子活性去抑制。该突变还观察到γ启动子活性的显著激活,提示存在一种阻遏物。精细诱变将这些活性解析到5'-UTR的不同区域。阶段选择活性定位于以核苷酸+13至+15为中心的区域。利用该序列进行的电泳迁移率变动分析证明,存在一种胎儿和红系特异性蛋白与之结合。5'-UTR的阻遏活性定位于串联的GATA样位点,这些位点似乎结合了两种蛋白的复合物,其中一种是红系转录因子GATA-1。这些结果表明,γ基因的5'-UTR包含对其转录和发育调控可能很重要的序列。

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