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NeuroD1 and Mash1 temporally regulate GnRH receptor gene expression in immortalized mouse gonadotrope cells

机译:NeuroD1和Mash1暂时调节永生化小鼠性腺生殖细胞中的GnRH受体基因表达

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摘要

Accurate spatial and temporal expression of gonadotrope-specific genes, such as the gonadotropin-releasing hormone receptor (GnRHR) gene, is critical for gonadotrope maturation. Herein, we show that a specific E-box in the mouse GnRHR promoter binds two group A basic-helix-loop-helix (bHLH) transcription factors. Mutation of this E-box decreases expression in mouse gonadotrope-derived αT3-1 and LβT2 cell lines. Microarray and western blots show that the bHLH transcription factor NeuroD1 is strongly expressed in the gonadotrope progenitor, αT3-1, whereas Mash1 is strongly expressed in the more mature gonadotrope, LβT2. Overexpression of NeuroD1 or Mash1 increases expression of the GnRHR gene or a multimer of the E-box and this increase is lost upon mutation of the E-box. Electrophoretic mobility shift assays reveal that the GnRHR E-box binds NeuroD1 from αT3-1 cells, but binds Mash1 from LβT2 cells. The sequential binding of different members of the group A bHLH transcription factor family to mouse GnRHR E-box 3 as the gonadotrope differentiates may represent a mechanism necessary for proper spatial and temporal expression of the GnRHR during gonadotrope development.
机译:促性腺激素特异性基因(例如促性腺激素释放激素受体(GnRHR)基因)的准确时空表达对于促性腺激素的成熟至关重要。本文中,我们显示了小鼠GnRHR启动子中的特定E-box结合了两个A组碱性螺旋-环-螺旋(bHLH)转录因子。此E-box的突变会降低小鼠促性腺激素衍生的αT3-1和LβT2细胞系中的表达。基因芯片和western印迹显示,bHLH转录因子NeuroD1在促性腺激素祖细胞αT3-1中强烈表达,而Mash1在更成熟的促性腺激素LβT2中强烈表达。 NeuroD1或Mash1的过表达增加了GnRHR基因或E-box的多聚体的表达,而这种增加在E-box突变后就消失了。电泳迁移率变动分析表明,GnRHR E-box结合来自αT3-1细胞的NeuroD1,但结合来自LβT2细胞的Mash1。随着促性腺激素的分化,A组bHLH转录因子家族的不同成员与小鼠GnRHR E-box 3的顺序结合可能代表了促性腺激素在发育过程中GnRHR的正确时空表达所必需的机制。

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