Molecular Virology Lab, Department of Microbiology, School of Biology, College of Sciences, University of Tehran, P.O. Box 14155-6455, Tehran, 1417614411, Iran.
Department of Biotechnology, College of Sciences, University of Tehran, Tehran, Iran.
J Neurovirol. 2023 Dec;29(6):669-677. doi: 10.1007/s13365-023-01174-8. Epub 2023 Sep 5.
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.
在潜伏感染期间,HSV-1 病毒仅生成一个单转录本 LAT,其编码六个 miRNA。γ-氨基丁酸能途径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 可能靶向 STXBP1 和 GABBR2 基因,这些基因是 GABA 能途径中的重要基因。利用 TargetScan 版本 5.2 和 RNA22 工具进行的生物信息学分析发现,编码 LAT 的 miRNA 可以影响 STXBP1 和 GABBR2 的转录本。为了评估编码 LAT 的候选 microRNA(即 miR-H3 和 miR-H4)的靶向作用,将 LAT 构建体转染到 HEK 293T 细胞中。通过实时 PCR 测定编码 LAT 的 microRNA 以及 STXBP1 和 GABBR2 的表达水平。最后,通过荧光素酶测定评估 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 表明 miR-H3 有可能靶向 STXBP1 和 GABBR2 基因的转录本,而 miR-H4 仅靶向 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,miR-H4、miR-H3 或 LAT 的过表达分别使 STXBP1 基因的表达平均降低了 0.0593 倍、0.237 倍和 0.84 倍。同样,miR-H3 或 miR-H4 的过表达使 GABBR2 的表达分别平均降低了 0.055 倍或 0.687 倍。值得注意的是,LAT 转录本对 GABBR2 3'UTR 的靶向作用没有检测到。通过荧光素酶测定评估了 LAT 编码的 microRNA 对 STXBP1 和 GABBR2 3'UTR 的靶向潜力。我们的结果表明,miR-H3 的过表达使 psiCHECK2 质粒中含有 STXBP1 或 GABBR2 3'UTR 基因的 Renilla 表达分别降低了 0.62 倍和 0.55 倍。miR-H4 降低了由 GABBR2 的 3'UTR 质粒调节的 Renilla 基因表达,但对由 STXBP1 的 3'UTR 质粒调节的 Renilla 基因表达没有影响。当 LAT 转录本过表达时,由于 STXBP1 的 3'UTR 的调节,Renilla 表达下降了 0.44 倍。然而,通过 GABBR2 的 3'UTR 的控制没有观察到显著的效果。