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在裂谷热病毒中新型前 microRNA 基因的计算机识别为胚胎-胎儿发育不良的新发病机制提供了线索。

In silico identification of novel pre-microRNA genes in Rift valley fever virus suggest new pathomechanisms for embryo-fetal dysgenesis.

机构信息

Institute of Novel and Emerging Infectious Diseases, Friedrich-Loeffler-Institut, Greifswald-Insel Riems, Germany.

出版信息

Virulence. 2024 Dec;15(1):2329447. doi: 10.1080/21505594.2024.2329447. Epub 2024 Mar 28.

DOI:10.1080/21505594.2024.2329447
PMID:38548679
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10984114/
Abstract

MicroRNAs (miRNAs) are small non-coding RNAs that regulate the post-transcriptional expression of target genes. Virus-encoded miRNAs play an important role in the replication of viruses, modulate gene expression in both the virus and host, and affect their persistence and immune evasion in hosts. This renders viral miRNAs as potential targets for therapeutic applications, especially against pathogenic viruses that infect humans and animals. Rift Valley fever virus (RVFV) is a mosquito-borne zoonotic RNA virus that causes severe disease in both humans and livestock. High mortality among newborn lambs and abortion storms are key characteristics of an RVF outbreak. To date, limited information is available on RVFV-derived miRNAs. In this study, computational methods were used to analyse the RVFV genome for putative pre-miRNA genes, which were then analysed for the presence of mature miRNAs. We detected 19 RVFV-encoded miRNAs and identified their potential mRNAs targets in sheep (, the most susceptible host. The identification of significantly enriched genes in association with RVFV miRNAs will help elucidate the molecular mechanisms underlying RVFV pathogenesis and potentially uncover novel drug targets for RVFV.

摘要

MicroRNAs (miRNAs) 是一类小的非编码 RNA,能够调控靶基因的转录后表达。病毒编码的 miRNAs 在病毒的复制过程中发挥着重要作用,调节病毒和宿主细胞中的基因表达,并影响病毒在宿主中的持续存在和免疫逃逸。这使得病毒 miRNAs 成为治疗应用的潜在靶点,特别是针对感染人类和动物的致病病毒。裂谷热病毒(RVFV)是一种蚊媒传播的人畜共患 RNA 病毒,可导致人和牲畜的严重疾病。新生羔羊的高死亡率和流产风暴是 RVF 爆发的关键特征。迄今为止,关于 RVFV 衍生的 miRNAs 的信息有限。在这项研究中,我们使用计算方法分析了 RVFV 基因组中的潜在 pre-miRNA 基因,然后分析了成熟 miRNAs 的存在情况。我们在绵羊中检测到 19 个 RVFV 编码的 miRNAs,并鉴定了它们在绵羊中的潜在靶基因(宿主)。与 RVFV miRNAs 相关的显著富集基因的鉴定将有助于阐明 RVFV 发病机制的分子机制,并可能为 RVFV 发现新的药物靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc7/10984114/c90004739e5f/KVIR_A_2329447_F0003b_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc7/10984114/7c62e271f72f/KVIR_A_2329447_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc7/10984114/c0a3377eb62d/KVIR_A_2329447_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc7/10984114/80ed6b02c263/KVIR_A_2329447_F0003a_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc7/10984114/c90004739e5f/KVIR_A_2329447_F0003b_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc7/10984114/7c62e271f72f/KVIR_A_2329447_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc7/10984114/c0a3377eb62d/KVIR_A_2329447_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc7/10984114/80ed6b02c263/KVIR_A_2329447_F0003a_B.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cbc7/10984114/c90004739e5f/KVIR_A_2329447_F0003b_B.jpg

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