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一种新型碱性螺旋-环-螺旋转录因子对胰岛素基因的组织特异性调控。

Tissue-specific regulation of the insulin gene by a novel basic helix-loop-helix transcription factor.

作者信息

Naya F J, Stellrecht C M, Tsai M J

机构信息

Department of Cell Biology, Baylor College of Medicine, Houston, Texas 77030, USA.

出版信息

Genes Dev. 1995 Apr 15;9(8):1009-19. doi: 10.1101/gad.9.8.1009.

Abstract

The insulin gene is one of the best paradigms of tissue-specific gene expression. It is developmentally regulated and is expressed exclusively in the pancreatic beta-cell. This restricted expression is directed by a tissue-specific enhancer, within the promoter, which contains an E-box sequence. The insulin E-box binds an islet-specific protein complex, termed 3a1. E-boxes bind proteins belonging to the basic helix-loop-helix (bHLH) family of transcription factors. The bHLH proteins function as potent transcriptional activators of tissue-specific genes by forming heterodimers between ubiquitous and cell-restricted family members. In addition, the cell-restricted bHLH members play an important role in specifying cell fate. To isolate the tissue-specific bHLH factor controlling insulin gene expression and study its role in islet cell differentiation, a modified yeast two-hybrid system was utilized to clone a novel bHLH factor, BETA2 (beta-cell E-box trans-activator 2), from a hamster insulin tumor (HIT) cell cDNA library. Northern analysis demonstrates that high-level expression of the BETA2 gene is restricted to pancreatic alpha- and beta-cell lines. As expected of tissue-specific bHLH members, BETA2 binds to the insulin E-box sequence with high affinity as a heterodimer with the ubiquitous bHLH factor E47. More importantly, antibody supershift experiments clearly show that BETA2 is a component of the native insulin E-box-binding complex. Transient transfection assays demonstrate that the BETA2/E47 heterodimer synergistically interacts with a neighboring beta-cell-specific complex to activate an insulin enhancer. In contrast, other bHLH factors such as MyoD and E47, which can bind to the insulin E-box with high affinity, fail to do so. Thus, a unique, cooperative interaction is the basis by which the insulin E-box enhancer discriminates between various bHLH factors to achieve tissue-specific activation of the insulin gene.

摘要

胰岛素基因是组织特异性基因表达的最佳范例之一。它受发育调控,仅在胰腺β细胞中表达。这种受限的表达由启动子内的组织特异性增强子指导,该增强子包含一个E盒序列。胰岛素E盒结合一种胰岛特异性蛋白复合物,称为3a1。E盒结合属于转录因子基本螺旋-环-螺旋(bHLH)家族的蛋白质。bHLH蛋白通过在普遍存在的和细胞限制性家族成员之间形成异二聚体,作为组织特异性基因的强效转录激活因子发挥作用。此外,细胞限制性bHLH成员在确定细胞命运中起重要作用。为了分离控制胰岛素基因表达的组织特异性bHLH因子并研究其在胰岛细胞分化中的作用,利用改良的酵母双杂交系统从仓鼠胰岛素瘤(HIT)细胞cDNA文库中克隆了一种新型bHLH因子BETA2(β细胞E盒反式激活因子2)。Northern分析表明,BETA2基因的高水平表达仅限于胰腺α细胞和β细胞系。正如对组织特异性bHLH成员所预期的那样,BETA2作为与普遍存在的bHLH因子E47的异二聚体,以高亲和力结合胰岛素E盒序列。更重要的是,抗体超迁移实验清楚地表明,BETA2是天然胰岛素E盒结合复合物的一个组成部分。瞬时转染实验表明,BETA2/E47异二聚体与相邻的β细胞特异性复合物协同相互作用,以激活胰岛素增强子。相比之下,其他能以高亲和力结合胰岛素E盒的bHLH因子,如MyoD和E47,则无法做到这一点。因此,一种独特的协同相互作用是胰岛素E盒增强子区分各种bHLH因子以实现胰岛素基因组织特异性激活的基础。

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