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海马体中与可塑性相关的基因调控和 SRF 依赖性转录的早期阶段。

Early phase of plasticity-related gene regulation and SRF dependent transcription in the hippocampus.

机构信息

Department of Functional Analysis, International School for Advanced Studies, Trieste, Italy.

出版信息

PLoS One. 2013 Jul 23;8(7):e68078. doi: 10.1371/journal.pone.0068078. Print 2013.

Abstract

Hippocampal organotypic cultures are a highly reliable in vitro model for studying neuroplasticity: in this paper, we analyze the early phase of the transcriptional response induced by a 20 µM gabazine treatment (GabT), a GABA-Ar antagonist, by using Affymetrix oligonucleotide microarray, RT-PCR based time-course and chromatin-immuno-precipitation. The transcriptome profiling revealed that the pool of genes up-regulated by GabT, besides being strongly related to the regulation of growth and synaptic transmission, is also endowed with neuro-protective and pro-survival properties. By using RT-PCR, we quantified a time-course of the transient expression for 33 of the highest up-regulated genes, with an average sampling rate of 10 minutes and covering the time interval [10∶90] minutes. The cluster analysis of the time-course disclosed the existence of three different dynamical patterns, one of which proved, in a statistical analysis based on results from previous works, to be significantly related with SRF-dependent regulation (p-value<0.05). The chromatin immunoprecipitation (chip) assay confirmed the rich presence of working CArG boxes in the genes belonging to the latter dynamical pattern and therefore validated the statistical analysis. Furthermore, an in silico analysis of the promoters revealed the presence of additional conserved CArG boxes upstream of the genes Nr4a1 and Rgs2. The chip assay confirmed a significant SRF signal in the Nr4a1 CArG box but not in the Rgs2 CArG box.

摘要

海马器官型培养物是研究神经可塑性的高度可靠的体外模型

在本文中,我们通过使用 Affymetrix 寡核苷酸微阵列、基于 RT-PCR 的时程分析和染色质免疫沉淀分析,分析了 20µM 加巴喷丁(GabT)处理(GabT),一种 GABA-A 受体拮抗剂,诱导的早期转录反应。基因表达谱分析表明, GabT 上调的基因库除了与生长和突触传递的调节密切相关外,还具有神经保护和生存促进特性。通过 RT-PCR,我们对 33 个上调最明显基因的瞬时表达进行了时间过程的定量,平均采样率为 10 分钟,涵盖了 [10∶90]分钟的时间间隔。时间过程的聚类分析揭示了三种不同动力学模式的存在,其中一种在基于先前工作结果的统计分析中被证明与 SRF 依赖性调节显著相关(p 值<0.05)。染色质免疫沉淀(chip)检测证实了属于后一种动力学模式的基因中富含工作 CArG 盒,因此验证了统计分析。此外,对启动子的计算机分析显示,在 Nr4a1 和 Rgs2 基因的上游存在其他保守的 CArG 盒。chip 检测证实了 Nr4a1 CArG 盒中存在显著的 SRF 信号,但 Rgs2 CArG 盒中没有。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c3e7/3720722/8caf5ecea5de/pone.0068078.g001.jpg

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