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Msx1 Homeodomain Protein Represses the αGSU and GnRH Receptor Genes During Gonadotrope Development

机译:Msx1 Homeodomain蛋白抑制性腺发育过程中的αGSU和GnRH受体基因。

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摘要

Multiple homeodomain transcription factors are crucial for pituitary organogenesis and cellular differentiation. A homeodomain repressor, Msx1, is expressed from the ventral aspect of the developing anterior pituitary and implicated in gonadotrope differentiation. Here, we find that Msx1 represses transcription of lineage-specific pituitary genes such as the common α-glycoprotein subunit (αGSU) and GnRH receptor (GnRHR) promoters in the mouse gonadotrope-derived cell lines, αT3-1 and LβT2. Repression of the mouse GnRHR promoter by Msx1 is mediated through a consensus-binding motif in the downstream activin regulatory element (DARE). Truncation and mutation analyses of the human αGSU promoter map Msx1 repression to a site at −114, located at the junctional regulatory element (JRE). Dlx activators are closely related to the Msx repressors, acting through the same elements, and Dlx3 and Dlx2 act as transcriptional activators for GnRHR and αGSU, respectively. Small interfering RNA knockdown of Msx1 in αT3-1 cells increases endogenous αGSU and GnRHR mRNA expression. Msx1 gene expression reaches its maximal expression at the rostral edge at e13.5. The subsequent decline in Msx1 expression specifically coincides with the onset of expression of both αGSU and GnRHR. The expression levels of both αGSU and GnRHR in Msx1-null mice at e18.5 are higher compared with wild type, further confirming a role for Msx1 in the repression of αGSU and GnRHR. In summary, Msx1 functions as a negative regulator early in pituitary development by repressing the gonadotrope-specific αGSU and GnRHR genes, but a temporal decline in Msx1 expression alleviates this repression allowing induction of GnRHR and αGSU, thus serving to time the onset of gonadotrope-specific gene program.
机译:多个同源域转录因子对于垂体器官发生和细胞分化至关重要。同源域阻遏物,Msx1,从发育中的垂体前叶的腹侧表达,并牵涉到性腺生殖分化。在这里,我们发现Msx1抑制小鼠性腺生长激素衍生的细胞系αT3-1和LβT2中特定于世系的垂体基因的转录,例如常见的α-糖蛋白亚基(αGSU)和GnRH受体(GnRHR)启动子。 Msx1抑制小鼠GnRHR启动子是通过下游激活素调节元件(DARE)中的共有结合基序介导的。人αGSU启动子的截断和突变分析将Msx1抑制定位到位于连接调节元件(JRE)的-114位。 Dlx激活剂与Msx阻遏物密切相关,通过相同的元件起作用,而Dlx3和Dlx2分别充当GnRHR和αGSU的转录激活剂。 αT3-1细胞中Msx1的小干扰RNA敲低会增加内源性αGSU和GnRHR mRNA表达。 Msx1基因表达在e13.5的延髓边缘达到最大表达。 Msx1表达的随后下降特别与αGSU和GnRHR的表达开始相吻合。与野生型相比,在e18.5时Msx1无表达的小鼠中αGSU和GnRHR的表达水平都较高,进一步证实了Msx1在抑制αGSU和GnRHR中的作用。总之,Msx1通过抑制促性腺激素特异的αGSU和GnRHR基因而在垂体早期发育中起负调节作用,但是Msx1表达的暂时下降减轻了这种抑制作用,从而诱导了GnRHR和αGSU,从而为促性腺激素-特定基因程序。

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