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通过基因芯片微阵列分析对与突触后致密组分相关的mRNA种类进行表征。

Characterization of mRNA species that are associated with postsynaptic density fraction by gene chip microarray analysis.

作者信息

Suzuki Tatsuo, Tian Qing Bao, Kuromitsu Junro, Kawai Takatoshi, Endo Shogo

机构信息

Department of Neuroplasticity, Institute on Aging and Adaptation, Shinshu University Graduate School of Medicine, 3-1-1 Asahi, Matsumoto 390-8621, Japan.

出版信息

Neurosci Res. 2007 Jan;57(1):61-85. doi: 10.1016/j.neures.2006.09.009. Epub 2006 Oct 17.

DOI:10.1016/j.neures.2006.09.009
PMID:17049655
Abstract

We previously reported the partial identification by random sequencing of mRNA species that are associated with the postsynaptic density (PSD) fraction prepared from the rat forebrain [Tian et al., 1999. Mol. Brain Res. 72, 147-157]. We report here further characterization by gene chip analysis of the PSD fraction-associated mRNAs, which were prepared in the presence of RNase inhibitor. We found that mRNAs encoding various postsynaptic proteins, such as channels, receptors for neurotransmitters and neuromodulators, proteins involved in signaling, scaffold and adaptor proteins and cytoskeletal proteins, were highly concentrated in the PSD fraction, whereas those encoding housekeeping proteins, such as enzymes in the glycolytic pathway, were not. We extracted approximately 1900 mRNA species that were highly concentrated in the PSD fraction. mRNAs related to certain neuronal diseases were also enriched in the PSD fraction. We also constructed a cDNA library using the PSD fraction-associated mRNAs as templates, and identified 1152 randomly selected clones by sequencing. Our data suggested that the PSD fraction-associated mRNAs are a very useful resource, in which a number of as yet uncharacterized mRNAs are concentrated. Identification and functional characterization of them are essential for complete understanding of synaptic function.

摘要

我们之前报道了通过对从大鼠前脑制备的突触后致密物(PSD)组分进行随机测序来部分鉴定与之相关的mRNA种类[田等人,1999年。《分子脑研究》72卷,第147 - 157页]。我们在此报告在存在RNase抑制剂的情况下制备的PSD组分相关mRNA的基因芯片分析的进一步特征。我们发现编码各种突触后蛋白的mRNA,如通道、神经递质和神经调质的受体、参与信号传导的蛋白、支架和衔接蛋白以及细胞骨架蛋白,在PSD组分中高度富集,而编码管家蛋白的mRNA,如糖酵解途径中的酶,则不然。我们提取了约1900种在PSD组分中高度富集的mRNA种类。与某些神经元疾病相关的mRNA在PSD组分中也有富集。我们还以PSD组分相关mRNA为模板构建了一个cDNA文库,并通过测序鉴定了随机选择的1152个克隆。我们的数据表明,PSD组分相关mRNA是一种非常有用的资源,其中集中了许多尚未表征的mRNA。对它们进行鉴定和功能表征对于全面理解突触功能至关重要。

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