首页> 美国卫生研究院文献>Data in Brief >Data on characterizing the gene expression patterns of neuronal ceroid lipofuscinosis genes: CLN1 CLN2 CLN3 CLN5 and their association to interneuron and neurotransmission markers: Parvalbumin and Somatostatin
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Data on characterizing the gene expression patterns of neuronal ceroid lipofuscinosis genes: CLN1 CLN2 CLN3 CLN5 and their association to interneuron and neurotransmission markers: Parvalbumin and Somatostatin

机译:表征神经元类脂褐质沉着病基因:CLN1CLN2CLN3CLN5的基因表达模式及其与中神经元和神经传递标记物:小白蛋白和生长抑素的关系的数据

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摘要

The article contains raw and analyzed data related to the research article “Neuronal ceroid lipofuscinosis genes, CLN2, CLN3, CLN5 are spatially and temporally co-expressed in a developing mouse brain” (Fabritius et al., 2014) [1]. The processed data gives an understanding of the development of the cell types that are mostly affected by defective function of CLN proteins, timing of expression of CLN1, CLN2, CLN3 and CLN5 genes in a murine model. The data shows relationship between the expression pattern of these genes during neural development. Immunohistochemistry was used to identify known interneuronal markers for neurotransmission and cell proliferation: parvalbumin, somatostatin subpopulations of interneurons. Non-radioactive in-situ hybridization detected CLN5 mRNA in the hippocampus. Throughout the development strong expression of CLN genes were identified in the germinal epithelium and in ventricle regions, cortex, hippocampus, and cerebellum. This provides supportive evidence that CLN1, CLN2, CLN3 and CLN5 genes may be involved in synaptic pruning.
机译:该文章包含与研究文章“在发育中的小鼠大脑中时空共表达神经元类固醇脂褐藻病基因,CLN2,CLN3,CLN5”有关的原始和分析数据(Fabritius等,2014)[1]。处理后的数据可以了解大多数受CLN蛋白功能缺陷影响的细胞类型的发育,鼠模型中CLN1,CLN2,CLN3和CLN5基因表达的时机。数据显示了神经发育过程中这些基因表达模式之间的关系。免疫组织化学被用来识别神经传递和细胞增殖的已知神经内标记物:小白蛋白,生长素抑制素亚群。非放射性原位杂交检测海马中的CLN5 mRNA。在整个发育过程中,在新生上皮以及脑室区域,皮质,海马和小脑中均发现了CLN基因的强表达。这提供了支持性证据,表明CLN1,CLN2,CLN3和CLN5基因可能与突触修剪有关。

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