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哺乳动物髓磷脂基因Opalin系统发育保守内含子区域中的少突胶质细胞增强子。

An oligodendrocyte enhancer in a phylogenetically conserved intron region of the mammalian myelin gene Opalin.

作者信息

Aruga Jun, Yoshikawa Fumio, Nozaki Yayoi, Sakaki Yoshiyuki, Toyoda Atsushi, Furuichi Teiichi

机构信息

Laboratory for Comparative Neurogenesis, RIKEN Brain Science Institute, Wako-shi, Saitama, JapanLaboratory for Molecular Neurogenesis, RIKEN Brain Science Institute, Wako-shi, Saitama, JapanSequence Technology Team, RIKEN Genomic Science Center, Yokohama, Japan.

出版信息

J Neurochem. 2007 Sep;102(5):1533-1547. doi: 10.1111/j.1471-4159.2007.04583.x. Epub 2007 Apr 17.

Abstract

Opalin is a transmembrane protein detected specifically in mammalian oligodendrocytes. Opalin homologs are found only in mammals and not in the genome sequences of other animal classes. We first determined the nucleotide sequences of Opalin orthologs and their flanking regions derived from four prosimians, a group of primitive primates. A global comparison revealed that an evolutionarily conserved region exists in the first intron of Opalin. When the conserved domain was assayed for its enhancer activity in transgenic mice, oligodendrocyte-directed expression was observed. In an oligodendroglial cell line, Oli-neu, the conserved domain showed oligodendrocyte-directed expression. The conserved domain is composed of eight subdomains, some of which contain binding sites for Myt1 and cAMP-response element binding protein (CREB). Deletion analysis and cotransfection experiments revealed that the subdomains have critical roles in Opalin gene expression. Over-expression of Myt1, treatment of the cell with leukemia inhibitory factor (LIF), and cAMP analog (CREB activator) enhanced the expression of endogenous Opalin in Oli-neu cells and activated the oligodendrocyte enhancer. These results suggest that LIF, cAMP signaling cascades and Myt1 play significant roles in the differentiation of oligodendrocytes through their action on the Opalin oligodendrocyte enhancer.

摘要

奥帕林蛋白是一种跨膜蛋白,专门在哺乳动物的少突胶质细胞中被检测到。奥帕林蛋白的同源物仅在哺乳动物中发现,而在其他动物类别的基因组序列中未发现。我们首先确定了来自四种原猴(一类原始灵长类动物)的奥帕林直系同源物及其侧翼区域的核苷酸序列。全局比较显示,奥帕林蛋白的第一个内含子中存在一个进化上保守的区域。当在转基因小鼠中检测该保守结构域的增强子活性时,观察到了少突胶质细胞定向表达。在少突胶质细胞系Oli-neu中,该保守结构域也显示出少突胶质细胞定向表达。该保守结构域由八个亚结构域组成,其中一些包含与Myt1和环磷酸腺苷反应元件结合蛋白(CREB)的结合位点。缺失分析和共转染实验表明,这些亚结构域在奥帕林蛋白基因表达中起关键作用。Myt1的过表达、用白血病抑制因子(LIF)处理细胞以及环磷酸腺苷类似物(CREB激活剂)增强了Oli-neu细胞中内源性奥帕林蛋白的表达,并激活了少突胶质细胞增强子。这些结果表明,LIF、环磷酸腺苷信号级联反应和Myt1通过作用于奥帕林蛋白少突胶质细胞增强子,在少突胶质细胞的分化中发挥重要作用。

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