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Enrichment of Circular RNA Expression Deregulation at the Transition to Recurrent Spontaneous Seizures in Experimental Temporal Lobe Epilepsy

机译:在实验颞叶癫痫中致胆发生自发癫痫发作的循环RNA表达放松症的富集

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Mesial temporal lobe epilepsy (mTLE) is a common form of epilepsy and is characterized by recurrent spontaneous seizures originating from the temporal lobe. The majority of mTLE patients develop pharmacoresistance to available anti-epileptic drugs (AEDs) while exhibiting severe pathological changes that can include hippocampal atrophy, neuronal death, gliosis and chronic seizures. The molecular mechanisms leading to mTLE remain incompletely understood, but are known to include defects in post-transcriptional gene expression regulation, including in non-coding RNAs (ncRNAs). Circular RNAs (circRNAs) are a class of recently rediscovered ncRNAs with high levels of expression in the brain and proposed roles in diverse neuronal processes. To explore a potential role for circRNAs in epilepsy, RNA-sequencing (RNA-seq) was performed on hippocampal tissue from a rat perforant pathway stimulation (PPS) model of TLE at different post-stimulation time points. This analysis revealed 218 differentially expressed (DE) circRNAs. Remarkably, the majority of these circRNAs were changed at the time of the occurrence of the first spontaneous seizure (DOFS). The expression pattern of two circRNAs, circ_Arhgap4 and circ_Nav3, was further validated and linked to miR-6328 and miR-10b-3p target regulation, respectively. This is the first study to examine the regulation of circRNAs during the development of epilepsy. It reveals an intriguing link between circRNA deregulation and the transition of brain networks into the state of spontaneous seizure activity. Together, our results provide a molecular framework for further understanding the role and mechanism-of-action of circRNAs in TLE.
机译:患者颞叶癫痫(咒语)是一种常见的癫痫形式,其特征是源自颞叶的复发性自发癫痫发作。大多数咒语患者发育脓疱病的抗癫痫药物(AED),同时表现出严重的病理变化,可包括海马萎缩,神经元死亡,脊髓源性和慢性癫痫发作。导致咒语的分子机制仍然不完全理解,但是已知包括转录后基因表达调控中的缺陷,包括在非编码RNA(NCRNA)中。圆形RNA(Circrna)是一类最近重新发现的NCRNA,在大脑中具有高水平的表达,并在不同的神经元过程中提出的作用。为了探讨癫痫中的CircRNA的潜在作用,在不同后刺激时间点的大鼠穿孔途径刺激(PPS)模型中对海马组织进行RNA测序(RNA-SEQ)。该分析显示218差异表达(de)Circrnas。值得注意的是,在发生第一次自发癫痫发作(DOF)时,这些Circrnas的大多数都发生了变化。两个CircrNA,Circ_arhgap4和Circ_Nav3的表达模式分别验证并与miR-6328和miR-10b-3p目标调节进行了验证并链接。这是第一次研究癫痫发育过程中核心克拉的调控。它揭示了CircrNA放松抑制与脑网络转变为自发癫痫发作活动状态之间的有趣链接。我们的结果在一起提供了进一步了解Circrnas在TLE中的作用和机制的分子框架。

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