Suppr超能文献

首次从严重急性呼吸综合征冠状病毒中发现的互补回文小RNA。

Complemented Palindromic Small RNAs First Discovered from SARS Coronavirus.

作者信息

Liu Chang, Chen Ze, Hu Yue, Ji Haishuo, Yu Deshui, Shen Wenyuan, Li Siyu, Ruan Jishou, Bu Wenjun, Gao Shan

机构信息

Laboratory of Medical Molecular Virology, School of Medicine, Nankai University, Tianjin 300071, China.

State Key Laboratory of Veterinary Etiological Biology and Key Laboratory of Veterinary Parasitology of Gansu Province, Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Science, Lanzhou 730046, China.

出版信息

Genes (Basel). 2018 Sep 5;9(9):442. doi: 10.3390/genes9090442.

Abstract

In this study, we report for the first time the existence of complemented palindromic small RNAs (cpsRNAs) and propose that cpsRNAs and palindromic small RNAs (psRNAs) constitute a novel class of small RNAs. The first discovered 19-nt cpsRNA UUAACAAGCUUGUUAAAGA, named SARS-CoV-cpsR-19, was detected from a 22-bp DNA complemented palindrome TCTTTAACAAGCTTGTTAAAGA in the severe acute respiratory syndrome coronavirus (SARS-CoV) genome. The phylogenetic analysis supported that this DNA complemented palindrome originated from bat betacoronavirus. The results of RNA interference (RNAi) experiments showed that one 19-nt segment corresponding to SARS-CoV-cpsR-19 significantly induced cell apoptosis. Using this joint analysis of the molecular function and phylogeny, our results suggested that SARS-CoV-cpsR-19 could play a role in SARS-CoV infection or pathogenesis. The discovery of cpsRNAs has paved a way to find novel markers for pathogen detection and to reveal the mechanisms underlying infection or pathogenesis from a different point of view. Researchers can use cpsRNAs to study the infection or pathogenesis of pathogenic viruses when these viruses are not available. The discovery of psRNAs and cpsRNAs, as a novel class of small RNAs, also inspire researchers to investigate DNA palindromes and DNA complemented palindromes with lengths of psRNAs and cpsRNAs in viral genomes.

摘要

在本研究中,我们首次报道了互补回文小RNA(cpsRNAs)的存在,并提出cpsRNAs和回文小RNA(psRNAs)构成了一类新型小RNA。首次发现的19个核苷酸的cpsRNA UUAACAAGCUUGUUAAAGA,命名为SARS-CoV-cpsR-19,是从严重急性呼吸综合征冠状病毒(SARS-CoV)基因组中一个22个碱基对的DNA互补回文序列TCTTTAACAAGCTTGTTAAAGA中检测到的。系统发育分析支持该DNA互补回文序列起源于蝙蝠β冠状病毒。RNA干扰(RNAi)实验结果表明,与SARS-CoV-cpsR-19对应的一个19个核苷酸片段显著诱导细胞凋亡。通过这种分子功能和系统发育的联合分析,我们的结果表明SARS-CoV-cpsR-19可能在SARS-CoV感染或发病机制中发挥作用。cpsRNAs的发现为寻找病原体检测的新标志物以及从不同角度揭示感染或发病机制奠定了基础。当无法获得致病病毒时,研究人员可以利用cpsRNAs研究致病病毒的感染或发病机制。psRNAs和cpsRNAs作为一类新型小RNA的发现,也激励研究人员研究病毒基因组中长度为psRNAs和cpsRNAs的DNA回文序列和DNA互补回文序列。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验