首页> 美国卫生研究院文献>The Journal of Neuroscience >Identification of a Smad4/YY1-Recognizedand BMP2-Responsive Transcriptional RegulatoryModule in the Promoter of Mouse GABA Transporter Subtype I (Gat1) Gene
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Identification of a Smad4/YY1-Recognizedand BMP2-Responsive Transcriptional RegulatoryModule in the Promoter of Mouse GABA Transporter Subtype I (Gat1) Gene

机译:小鼠GABA转运蛋白亚型I(Gat1)基因启动子中的Smad4 / YY1公认和BMP2响应转录调控模块的鉴定。

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摘要

GABAergic dysfunction is implicated in a variety of neurodevelopmental and psychiatric disorders. The mechanisms underlying GABAergic differentiation, however, are not well understood. GABA transporter 1 (Gat1; Slc6a1) is an essential component of the GABAergic system, and its ectopic mRNA expression may be responsible for GABAergic malfunction under different pathological conditions. Thus, monitoring the transcriptional regulation of gat1 may help to elucidate the mechanisms that govern the differentiation of GABAergic neurons. In this study, we identified a promoter region that is sufficient to recapitulate endogenous gat1 expression in transgenic mice. A 46 bp cis-regulator in the promoter sequence was responsible for the stimulation of bone morphogenetic protein-2 (BMP2) on gat1 expression in cortical cortex. Furthermore, our study demonstrated that Smad4 and YY1 are physically bound to the element and mediate both the negative and positive regulatory effects in which BMP2 can affect the balance. In summary, we have identified a Smad4/YY1-based bidirectional regulation model for GABAergic gene transcription and demonstrated a molecular cue important for the differentiation of GABAergic neurons.
机译:GABA能功能障碍与多种神经发育和精神疾病有关。然而,对GABA能分化的机制尚不十分了解。 GABA转运蛋白1(Gat1; Slc6a1)是GABA能系统的重要组成部分,其异位mRNA表达可能在不同病理条件下引起GABA能功能异常。因此,监测gat1的转录调控可能有助于阐明控制GABA能神经元分化的机制。在这项研究中,我们确定了一个足以重现转基因小鼠中内源性gat1表达的启动子区域。启动子序列中一个46 bp的顺式调节子负责刺激皮质Gat1表达上的骨形态发生蛋白2(BMP2)。此外,我们的研究表明Smad4和YY1在物理上与该元素结合,并介导BMP2可以影响平衡的负面和正面调节作用。总之,我们已经确定了基于Smad4 / YY1的GABA能基因转录的双向调控模型,并证明了对GABA能神经元分化重要的分子提示。

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