HSV-1 潜伏期相关转录本 miR-H3 和 miR-H4 的靶标是 STXBP1 和 GABBR2 基因。

IF 2.3 4区 医学 Q3 NEUROSCIENCES Journal of NeuroVirology Pub Date : 2023-12-01 Epub Date: 2023-09-05 DOI:10.1007/s13365-023-01174-8
Karrar Mahmood Shaker Al-Khfaji, Nika Kooshki Zamani, Ehsan Arefian
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引用次数: 0

摘要

在潜伏感染期间,HSV-1 病毒只产生一个转录本 LAT,它编码六种 miRNA。GABA 能通路信号系统是一种重要的细胞信号通路,受多种治疗靶点和一些脑部疾病(如癫痫)的影响。本研究发现,编码 LAT 的 miRNA 可能以 STXBP1 和 GABBR2 基因为靶标,而这两个基因是 GABA 能通路中的重要基因之一。利用 TargetScan 5.2 版和 RNA22 工具进行的生物信息学分析发现,编码 LAT 的 miRNA 可影响 STXBP1 和 GABBR2 转录本。为了评估编码 LAT 的候选 microRNA(即 miR-H3 和 miR-H4)的靶向效应,将 LAT 构建体转染到 HEK 293T 细胞中。通过实时 PCR 检测了编码 LAT 的 microRNA 以及 STXBP1 和 GABBR2 的表达水平。最后,通过荧光素酶实验评估了 LAT 编码的 microRNA 对 STXBP1 和 GABBR2 3'UTR 的靶向潜力。在本研究中,生物信息学工具 TargetScan 显示,miR-H3 有可能靶向 STXBP1 和 GABBR2 基因的转录本,而 miR-H4 只靶向 GABBR2。另一方面,生物信息学工具 RNA22 验证了 miR-H3 和 miR-H4 对 STXBP1 和 GABBR2 的潜在靶向作用。我们的研究结果表明,过表达 miR-H4、miR-H3 或 LAT 会显著降低 STXBP1 基因的表达,平均降幅分别为 0.0593 倍、0.237 倍和 0.84 倍。同样,过表达 miR-H3 或 miR-H4 会使 GABBR2 的表达分别平均减少 0.055 倍或 0.687 倍。值得注意的是,用 LAT 转录本靶向 GABBR2 3'UTR 没有检测到影响。用荧光素酶试验评估了 LAT 编码的 microRNA 靶向 STXBP1 和 GABBR2 3'UTR 的潜力。我们的结果表明,miR-H3 的过量表达会使带有 STXBP1 或 GABBR2 3'UTR 基因的 psiCHECK2 质粒中的 Renilla 表达量分别降低 0.62 倍和 0.55 倍;miR-H4 会降低 GABBR2 3'UTR 质粒调控的 Renilla 基因表达量,但对 STXBP1 3'UTR 调控的 Renilla 基因表达量没有影响。当过量表达 LAT 转录本时,由于 STXBP1 的 3'UTR 的调控,Renilla 基因的表达量减少了 0.44 倍。然而,通过控制 GABBR2 的 3'UTR 没有观察到明显的影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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HSV-1 latency-associated transcript miR-H3 and miR-H4 target STXBP1 and GABBR2 genes.

During latent infection, the HSV-1 virus generates only a single transcript, LAT, which encodes six miRNAs. The GABAergic pathway signaling system is an essential cell signaling pathway influenced by various therapeutic targets and some brain disorders, such as epilepsy. This study found that miRNAs encoding LAT might target the STXBP1 and GABBR2 genes, which are among the significant genes in the GABAergic pathway. Bioinformatic analysis utilizing TargetScan version 5.2 and the RNA22 tools uncovered miRNAs encoding LAT that can influence STXBP1 and GABBR2 transcripts. To evaluate the targeting effect of candidate microRNAs encoding LAT, namely, miR-H3 and miR-H4, LAT constructs were transfected into HEK 293T cells. The expression levels of microRNAs encoding LAT, as well as STXBP1 and GABBR2, were assayed by real-time PCR. Finally, the targeting potential of STXBP1 and GABBR2 3'UTR by LAT-encoded microRNAs was evaluated by the luciferase assay. In the current study, the bioinformatic tool TargetScan demonstrated that miR-H3 has the potential to target the transcripts of the STXBP1 and GABBR2 genes, whereas miR-H4 solely targeted GABBR2. On the other hand, the bioinformatic tool RNA22 validated the potential targeting of STXBP1 and GABBR2 by miR-H3 and miR-H4. Our findings showed that overexpression of miR-H4, miR-H3, or LAT significantly decreased STXBP1 gene expression by an average of 0.0593-fold, 0.237-fold, and 0.84-fold, respectively. Similarly, overexpression of miR-H3 or miR-H4 decreased GABBR2 expression by an average of 0.055- or 0.687-fold, respectively. Notably, targeting the GABBR2 3'UTR with the LAT transcript had no detectable effect. The evaluation of the targeting potential of STXBP1 and GABBR2 3'UTR by microRNAs encoded by LAT was conducted with a luciferase assay. Our results showed that miR-H3 overexpression reduces Renilla expression in psiCHECK2 plasmids with STXBP1 or GABBR2 3'UTR genes by 0.62- and 0.55-fold, respectively. miR-H4 reduced Renilla gene expression regulated by GABBR2's 3'UTR plasmid but had no effect on the Renilla gene expression regulated by STXBP1's 3'UTR. When the LAT transcript was overexpressed, there was a decrease in Renilla expression by 0.44-fold because of the regulation of STXBP1's 3'UTR. However, there was no significant effect observed through the control of GABBR2's 3'UTR.

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来源期刊
Journal of NeuroVirology
Journal of NeuroVirology 医学-病毒学
CiteScore
6.60
自引率
3.10%
发文量
77
审稿时长
6-12 weeks
期刊介绍: The Journal of NeuroVirology (JNV) provides a unique platform for the publication of high-quality basic science and clinical studies on the molecular biology and pathogenesis of viral infections of the nervous system, and for reporting on the development of novel therapeutic strategies using neurotropic viral vectors. The Journal also emphasizes publication of non-viral infections that affect the central nervous system. The Journal publishes original research articles, reviews, case reports, coverage of various scientific meetings, along with supplements and special issues on selected subjects. The Journal is currently accepting submissions of original work from the following basic and clinical research areas: Aging & Neurodegeneration, Apoptosis, CNS Signal Transduction, Emerging CNS Infections, Molecular Virology, Neural-Immune Interaction, Novel Diagnostics, Novel Therapeutics, Stem Cell Biology, Transmissable Encephalopathies/Prion, Vaccine Development, Viral Genomics, Viral Neurooncology, Viral Neurochemistry, Viral Neuroimmunology, Viral Neuropharmacology.
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