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从小RNA测序数据中对病毒小RNA进行系统鉴定和表征。

Systematic identification and characterization of viral small RNAs from small RNA-Seq data.

作者信息

Cai Zena, Fu Ping, Xu Lihua, Deng Li, Peng Yousong

机构信息

Hunan Provincial Key Laboratory of Medical Virology, Bioinformatics Center, College of Biology, Hunan University, Changsha, China.

Internal Medicine-Neurology, The Third Hospital of Changsha, Changsha, China.

出版信息

J Med Virol. 2023 Mar;95(3):e28617. doi: 10.1002/jmv.28617.

Abstract

Virus-encoded small RNAs (vsRNAs) have been reported to play an important role in viral infections. Unfortunately, there is still a lack of a systematic characterization and resource of vsRNAs. Herein, we identified a total of 19 734 high-confidence vsRNAs including 2746 microRNAs (miRNAs) in 64 viral species from more than 800 samples of public small RNA-Seq data. The number of vsRNAs identified in viruses varied from 1 to 2489 with a median of 170. The length distribution of vsRNAs peaked at 21 and 22 nt. Plant viruses were found to express larger number and higher levels of vsRNAs than those of animal viruses. Besides, the number of vsRNAs identified increased as the viral infection persisted. Interestingly, the vsRNA showed strong expression specificity as little overlap was observed among vsRNAs identified in different strains of a virus, or in different hosts, cells, or tissues infected by the same virus. Little conservation was observed among vsRNAs of different viruses. The viral miRNAs were found to interact with host genes involved in multiple biological processes related to organization, development, action potential, polarity establishment, methylation, immune response, gene regulation, localization, and so on. To facilitate the usage of vsRNAs, a database named vsRNAdb was built for organizing and storing vsRNAs which is available at http://www.computationalbiology.cn/vsRNAdb/#/vsRNAdb/#/. Overall, the study deepens our understanding about the diversity and complexity of vsRNAs and provides a rich resource for further studies of vsRNAs.

摘要

病毒编码的小RNA(vsRNAs)已被报道在病毒感染中发挥重要作用。遗憾的是,目前仍缺乏对vsRNAs的系统表征和资源。在此,我们从800多个公开的小RNA测序数据样本中,在64种病毒中总共鉴定出19734个高可信度的vsRNAs,其中包括2746个 microRNA(miRNA)。在病毒中鉴定出的vsRNAs数量从1到2489不等,中位数为170。vsRNAs的长度分布在21和22nt处达到峰值。发现植物病毒比动物病毒表达的vsRNAs数量更多、水平更高。此外,随着病毒感染持续,鉴定出的vsRNAs数量增加。有趣的是,vsRNA表现出很强的表达特异性,在同一病毒的不同毒株中,或在同一病毒感染的不同宿主、细胞或组织中鉴定出的vsRNAs之间几乎没有重叠。不同病毒的vsRNAs之间几乎没有保守性。发现病毒miRNA与参与多个生物学过程的宿主基因相互作用,这些生物学过程包括组织、发育、动作电位、极性建立、甲基化、免疫反应、基因调控、定位等。为了便于vsRNAs的使用,构建了一个名为vsRNAdb的数据库来组织和存储vsRNAs,可在http://www.computationalbiology.cn/vsRNAdb/#/vsRNAdb/#/获取。总体而言,该研究加深了我们对vsRNAs多样性和复杂性的理解,并为进一步研究vsRNAs提供了丰富的资源。

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