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PAX6基因由碱性螺旋-环-螺旋转录因子NeuroD/BETA2激活。

The PAX6 gene is activated by the basic helix-loop-helix transcription factor NeuroD/BETA2.

作者信息

Marsich Eleonora, Vetere Amedeo, Di Piazza Matteo, Tell Gianluca, Paoletti Sergio

机构信息

Department of Biochemistry, Biophysics and Macromolecular Chemistry, University of Trieste, Italy.

出版信息

Biochem J. 2003 Dec 15;376(Pt 3):707-15. doi: 10.1042/BJ20031021.

Abstract

PAX6 is a transcription factor that plays an important role during pancreatic morphogenesis. The aim of the present study is to identify the upstream activator(s) of the PAX6 gene possibly involved in the early stages of pancreatic differentiation. Recently, individual elements regulating PAX6 gene activity in the pancreas have been identified in a 1100 bp Spe / Hin cII fragment 4.6 kb upstream of exon 0. Preliminary sequence analysis of this region revealed some potential DNA-binding sites (E boxes) specific for the binding of basic helix-loop-helix transcription factors. By using electrophoretic mobility shift assays, we demonstrated that both nuclear protein extracts from insulin-secreting RINm5F cells and in vitro -translated NeuroD/BETA2 can bind specifically to these E boxes. Furthermore, by transient transfection experiments we demonstrated that the expression of basic helix-loop-helix transcription factor NeuroD/BETA2 can induce activation of the PAX6 promoter in the NIH-3T3 cell line. Thus we show that NeuroD/BETA2 is involved in the activation of the expression of PAX6 through E boxes in the PAX6 promoter localized in a 1.1 kb sequence within the 4.6 kb untranslated region upstream of exon 0.

摘要

PAX6是一种转录因子,在胰腺形态发生过程中发挥重要作用。本研究的目的是鉴定可能参与胰腺分化早期阶段的PAX6基因的上游激活因子。最近,在第0外显子上游4.6 kb处的一个1100 bp的Spe/Hin cII片段中,已鉴定出调节胰腺中PAX6基因活性的单个元件。对该区域的初步序列分析揭示了一些潜在的DNA结合位点(E盒),这些位点是碱性螺旋-环-螺旋转录因子特异性结合的位点。通过电泳迁移率变动分析,我们证明了来自胰岛素分泌型RINm5F细胞的核蛋白提取物和体外翻译的NeuroD/BETA2都能特异性地结合这些E盒。此外,通过瞬时转染实验,我们证明了碱性螺旋-环-螺旋转录因子NeuroD/BETA2的表达可以诱导PAX6启动子在NIH-3T3细胞系中的激活。因此,我们表明NeuroD/BETA2通过位于第0外显子上游4.6 kb非翻译区内1.1 kb序列中的PAX6启动子中的E盒参与PAX6表达的激活。

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