首页> 美国卫生研究院文献>Frontiers in Molecular Neuroscience >Is Arc mRNA Unique: A Search for mRNAs That Localize to the Distal Dendrites of Dentate Gyrus Granule Cells Following Neural Activity
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Is Arc mRNA Unique: A Search for mRNAs That Localize to the Distal Dendrites of Dentate Gyrus Granule Cells Following Neural Activity

机译:是弧mRNA是独特的:搜索神经活动后本地化到齿状回颗粒细胞远端树突的mRNA的搜索。

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摘要

There have been several attempts to identify which RNAs are localized to dendrites; however, no study has determined which RNAs localize to the dendrites following the induction of synaptic activity. We sought to identify all RNA transcripts that localize to the distal dendrites of dentate gyrus granule cells following unilateral high frequency stimulation of the perforant pathway (pp-HFS) using Sprague Dawley rats. We then utilized laser microdissection (LMD) to very accurately dissect out the distal 2/3rds of the molecular layer (ML), which contains these dendrites, without contamination from the granule cell layer, 2 and 4 h post pp-HFS. Next, we purified and amplified RNA from the ML and performed an unbiased screen for 27,000 RNA transcripts using Affymetrix microarrays. We determined that Activity Regulated Cytoskeletal Protein (Arc/Arg3.1) mRNA, exhibited the greatest fold increase in the ML at both timepoints (2 and 4 h). In total, we identified 31 transcripts that increased their levels within the ML following pp-HFS across the two timepoints. Of particular interest is that one of these identified transcripts was an unprocessed micro-RNA (pri-miR132). Fluorescent in situ hybridization and qRT-PCR were used to confirm some of these candidate transcripts. Our data indicate Arc is a unique activity dependent gene, due to the magnitude that its activity dependent transcript localizes to the dendrites. Our study determined other activity dependent transcripts likely localize to the dendrites following neural activity, but do so with lower efficiency compared to Arc.
机译:已经进行了多种尝试来鉴定哪些RNA定位于树突中。但是,尚无研究确定在诱导突触活性后哪些RNA定位于树突。我们试图确定单侧高频刺激穿孔路径(pp-HFS)后使用Sprague Dawley大鼠定位于齿状回颗粒细胞远端树突的所有RNA转录物。然后,我们在pp-HFS后2和4小时内利用激光显微切割(LMD)非常精确地解剖了分子层(ML)的远端2 / 3rd,其中包含这些树突,而不受颗粒细胞层的污染。接下来,我们从ML中纯化和扩增了RNA,并使用Affymetrix微阵列对27,000个RNA转录本进行了无偏筛选。我们确定活动调节细胞骨架蛋白(Arc / Arg3.1)mRNA,在两个时间点(2和4 h)表现出最大的ML倍数增加。总共,我们确定了在两个时间点的pp-HFS之后增加ML中其水平的31个转录物。特别令人感兴趣的是,这些鉴定出的转录本之一是未加工的微RNA(pri-miR132)。荧光原位杂交和qRT-PCR用于确认其中一些候选转录本。我们的数据表明Arc是一个独特的活性依赖基因,这是由于Arc的活性依赖转录本位于树突中的程度。我们的研究确定了其他依赖神经活动的转录本可能在神经活动后定位在树突上,但与Arc相比效率较低。

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