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首页> 外文期刊>Journal of Neurochemistry: Offical Journal of the International Society for Neurochemistry >A novel seven transmembrane receptor induced during the early steps of astrocyte differentiation identified by differential expression.
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A novel seven transmembrane receptor induced during the early steps of astrocyte differentiation identified by differential expression.

机译:星形胶质细胞分化的早期步骤中诱导的新型七跨膜受体通过差异表达确定。

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The rat glial progenitor cell line CG-4 can be induced to differentiate into either oligodendrocytes or type-2 astrocytes. In order to identify genes whose expression varies coincident with such phenotypic differentiation, we employed representational difference analysis (RDA) of mRNA. Here, we report 38 cDNAs induced in type-2 astrocytes, oligodendrocytes, or both differentiated states. Among these were known transcription factors, membrane receptors, extracellular matrix proteins, secreted signaling modulators, chromatin regulators and myelin sheath components. In addition several novel genes were identified; among these was a gene induced during the very early stages of astrocyte differentiation that we have named Ieda (induced early in differentiating astrocytes). Several Ieda transcripts were detected by RT-PCR, and appeared to be produced by alternative splicing and promoter usage. The protein deduced from the longest Ieda mRNA exhibited sequence features characteristic of G-protein coupled receptors, including seven putative transmembrane domains, while the shorter Ieda transcripts encoded proteins that lacked several transmembrane segments. In the adult rat, Ieda transcripts were found exclusively in brain and testis. In the developing rat brain, Ieda expression was first detected at embryonic day 16, that is two days before the first appearance of mature astrocytes. Thus, this approach has yielded a potential source of markers for differentiation states of these two cellular types as well as genes predicted to be functionally involved in the differentiation process itself.
机译:可以诱导大鼠神经胶质祖细胞系CG-4分化为少突胶质细胞或2型星形胶质细胞。为了鉴定其表达随这种表型分化而变化的基因,我们采用了mRNA的代表性差异分析(RDA)。在这里,我们报告在2型星形胶质细胞,少突胶质细胞或两种分化状态下诱导的38个cDNA。其中已知的转录因子,膜受体,细胞外基质蛋白,分泌的信号传导调节剂,染色质调节剂和髓鞘鞘成分。此外,还鉴定了几种新基因。其中一个是在星形胶质细胞分化的早期阶段诱导的基因,我们将其命名为Ieda(在分化星形胶质细胞的早期诱导)。通过RT-PCR检测到多个Ieda转录本,似乎是通过选择性剪接和启动子产生的。从最长的Ieda mRNA推导的蛋白质表现出具有G蛋白偶联受体特征的序列特征,包括七个假定的跨膜结构域,而较短的Ieda转录本编码的蛋白质缺乏几个跨膜片段。在成年大鼠中,仅在大脑和睾丸中发现了Ieda转录本。在发育中的大鼠大脑中,首先在胚胎第16天即成熟的星形胶质细胞首次出现前两天检测到Ieda表达。因此,该方法已经产生了用于这两种细胞类型的分化状态的标记物的潜在来源,以及被预测在功能上参与分化过程本身的基因。

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