首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >An astrocyte-specific enhancer of the aquaporin-4 gene functions through a consensus sequence of POU transcription factors in concert with multiple upstream elements.
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An astrocyte-specific enhancer of the aquaporin-4 gene functions through a consensus sequence of POU transcription factors in concert with multiple upstream elements.

机译:Aquaporin-4基因的星形细胞特异性增强剂通过与多个上游元件的音乐会的POU转录因子共有序列函数。

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摘要

Aquaporin-4, a predominant water channel in the brain, is specifically expressed in astrocyte endfeet and plays a central role in water homeostasis, neuronal activity, and cell migration in the brain. It has two dominant isoforms called M1 and M23, whose mRNA is driven by distinct promoters located upstream of exons 0 and 1 of the aquaporin-4 gene, respectively. To identify cis-acting elements responsible for the astrocyte-specific transcription of M1 mRNA, the promoter activity of the 5'-flanking region upstream of exon 0 in primary cultured mouse astrocytes was examined by luciferase assay, and sequences, where nuclear factors bind, were identified by electrophoretic mobility shift assay. An astrocyte-specific activity enhancing transcription from the M1 promoter was observed within ~2 kb from the transcriptional start sites of M1 mRNA. At least five elements clustered within the 286-bp region were found to function as a novel astrocyte-specific enhancer. Among the five elements, a consensus sequence of Pit-1/Oct/Unc-86 (POU) transcription factors was indispensable to the astrocyte-specific enhancer since disruption of the POU motif completely abolished the enhancer activity in astrocytes. However, the POU motif alone had little activity, indicating the requirement for cooperation with other upstream elements to exert full enhancer activity.
机译:Aquaporin-4,大脑中的主要水通道,在星形胶质细胞终止中特异性地表达,在脑稳态,神经元活动和大脑中的细胞迁移中起着核心作用。它具有两个称为M1和M23的显性异构型,其MRNA分别由位于外显子-4基因的上游的不同启动子驱动。为了鉴定负责M1 mRNA的星形胶质细胞特异性转录的顺式作用元件,通过荧光素酶测定检测在初级培养的小鼠星形胶质细胞上游的5'-侧翼区域的启动子活性,以及​​核因子结合的序列,通过电泳迁移率移位测定鉴定。从M1 mRNA的转录开始位点在〜2kb内观察到从M1启动子的转录转录的星形胶质细胞特异性活性。发现在286-BP区域内聚集的至少五种元素用作新的星形胶质细胞特异性增强剂。在五个要素中,坑-1 / OCT / UNC-86(POU)转录因子的共有序列对于星形胶质细胞特异性增强剂是必不可少的,因为POU主题的破坏完全废除了星形胶质细胞的增强剂活性。然而,单独的POU主题有很少的活动,表明要求与其他上游元素合作施加全增强者活动。

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