de Solis Christopher A, Morales Anna A, Hosek Matthew P, Partin Alex C, Ploski Jonathan E
School of Behavioral and Brain Sciences and the Department of Molecular & Cell Biology, University of Texas at Dallas, Richardson, TX, United States.
UT Southwestern Medical Center, Dallas, TX, United States.
Front Mol Neurosci. 2017 Oct 10;10:314. doi: 10.3389/fnmol.2017.00314. eCollection 2017.
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 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.
已经有多项研究试图确定哪些RNA定位于树突;然而,尚无研究确定在突触活动诱导后哪些RNA定位于树突。我们试图使用Sprague Dawley大鼠,在单侧高频刺激穿通通路(pp-HFS)后,确定定位于齿状回颗粒细胞远端树突的所有RNA转录本。然后,我们利用激光显微切割(LMD)在pp-HFS后2小时和4小时,非常精确地切割出分子层(ML)的远端2/3,该区域包含这些树突,且不受颗粒细胞层的污染。接下来,我们从ML中纯化并扩增RNA,并使用Affymetrix微阵列对27000个RNA转录本进行无偏差筛选。我们确定,活性调节细胞骨架蛋白(Arc/Arg3.1)mRNA在两个时间点(2小时和4小时)的ML中呈现出最大的倍数增加。总共,我们鉴定出31个转录本,它们在两个时间点的pp-HFS后在ML中的水平有所增加。特别有趣的是,这些鉴定出的转录本之一是一个未加工的微小RNA(pri-miR132)。荧光杂交和qRT-PCR被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性基因,因为其活性依赖性转录本定位于树突的程度很高。我们的研究确定,其他活性依赖性转录本在神经活动后可能定位于树突,但与Arc相比,其效率较低。