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首页> 外文期刊>Journal of Molecular Biology >Expression of Connexin47 in oligodendrocytes is regulated by the Sox10 transcription factor.
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Expression of Connexin47 in oligodendrocytes is regulated by the Sox10 transcription factor.

机译:连接蛋白47在少突胶质细胞中的表达受Sox10转录因子的调节。

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In the central nervous system, Connexin32 and Connexin47 are confined to oligodendrocytes where they contribute to myelin formation and maintenance, and are essential for establishing a functional glial syncytium that ensures ionic homeostasis. Despite their importance, not much is known about the regulation of connexin gene expression in oligodendrocytes. Here, we identify group E Sox proteins, in particular Sox10, as essential transcriptional regulators of both connexins. Not only was expression of Connexin32 and Connexin47 severely compromised in spinal cords of mouse mutants with reduced amounts of group E Sox proteins. Sox10 also stimulated in transient transfections the Connexin32 promoter as well as Connexin47 promoter 1b which is the main Connexin47 promoter active in the postnatal spinal cord. Detailed characterization of Connexin47 promoter 1b identified a single monomer binding site that mediated Sox10-dependent promoter activation. The region containing this binding site was also occupied by endogenous Sox10 in 33B oligodendroglioma cells. These results add Connexin47 and Connexin32 to the list of Sox10 target genes and argue that Sox10 may influence transcription of many terminal differentiation and myelination genes in oligodendrocytes as an essential regulatory component of the myelination program.
机译:在中枢神经系统中,Connexin32和Connexin47被限制在少突胶质细胞中,在那里它们有助于髓磷脂的形成和维持,并且对于建立能确保离子稳态的功能性胶质合胞体至关重要。尽管它们很重要,但对少突胶质细胞中连接蛋白基因表达的调控知之甚少。在这里,我们确定E组Sox蛋白,特别是Sox10,是这两种连接蛋白的必需转录调节因子。具有降低的E组Sox蛋白量的小鼠突变体的脊髓中不仅严重破坏了Connexin32和Connexin47的表达。 Sox10还可以在瞬时转染中刺激Connexin32启动子以及Connexin47启动子1b,后者是在出生后脊髓中活跃的主要Connexin47启动子。 Connexin47启动子1b的详细表征,确定了一个介导Sox10依赖的启动子激活的单体结合位点。含有该结合位点的区域在33B少突胶质细胞瘤细胞中也被内源性Sox10占据。这些结果将Connexin47和Connexin32添加到Sox10目标基因列表中,并认为Sox10可能影响少突胶质细胞中许多末端分化和髓鞘形成基因的转录,这是髓鞘形成程序的重要调控成分。

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