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一种针对不同亚型甲型流感病毒感染的细胞 RNA 编辑活性的综合研究。

A comprehensive study on cellular RNA editing activity in response to infections with different subtypes of influenza a viruses.

机构信息

Key Laboratory of Molecular Virology and Immunology, Institute Pasteur of Shanghai, Chinese Academy of Sciences, Shanghai, 20031, China.

National Engineering Research Center For the Emergence Drugs, Beijing Institute of Pharmacology and Toxicology, Beijing, 100850, China.

出版信息

BMC Genomics. 2018 Jan 19;19(Suppl 1):925. doi: 10.1186/s12864-017-4330-1.

Abstract

BACKGROUND

RNA editing is an important mechanism that expands the diversity and complexity of genetic codes. The conversions of adenosine (A) to inosine (I) and cytosine (C) to uridine (U) are two prominent types of RNA editing in animals. The roles of RNA editing events have been implicated in important biological pathways. Cellular RNA editing activity in response to influenza A virus infection has not been fully characterized in human and avian hosts. This study was designed as a big data analysis to investigate the role and response of RNA editing in epithelial cells during the course of infection with various subtypes of influenza A viruses.

RESULTS

Using a bioinformatics pipeline modified from our previous study, we characterized the profiles of A-to-I and C-to-U RNA editing events in human epithelial cells during the course of influenza A virus infection. Our results revealed a striking diversity of A-to-I RNA editing activities in human epithelial cells in responses to different subtypes of influenza A viruses. The infection of H1N1 and H3N2 significantly up-regulated normalized A-to-I RNA editing levels in human epithelial cells, whereas that of H5N1 did not change it and H7N9 infection significantly down-regulated normalized A-to-I editing level in A549 cells. Next, the expression levels of ADAR and APOBEC enzymes responsible for A-to-I and C-to-U RNA editing during the course of virus infection were examined. The increase of A-to-I RNA editing activities in infections with some influenza A viruses (H1N1 and H3N2) is linked to the up-regulation of ADAR1 but not ADAR2. Further, the pattern recognition receptors of human epithelial cells infected with H1N1, H3N2, H5N1 and H7N9 were examined. Variable responsive changes in gene expression were observed with RIG-I like receptors and Toll like receptors. Finally, the effect of influenza A virus infection on cellular RNA editing activity was also analyzed in avian hosts.

CONCLUSION

This work represents the first comprehensive study of cellular RNA editing activity in response to different influenza A virus infections in human and avian hosts, highlighting the critical role of RNA editing in innate immune response and the pathogenicity of different subtypes of influenza A viruses.

摘要

背景

RNA 编辑是一种重要的机制,可扩大遗传密码的多样性和复杂性。在动物中,两种突出的 RNA 编辑类型是腺苷(A)向肌苷(I)和胞嘧啶(C)向尿嘧啶(U)的转换。RNA 编辑事件的作用已被牵连到重要的生物途径中。在人类和禽类宿主中,尚未充分描述细胞 RNA 编辑活性对甲型流感病毒感染的反应。本研究旨在通过大数据分析,研究各种亚型甲型流感病毒感染过程中上皮细胞中 RNA 编辑的作用和反应。

结果

使用我们之前研究中修改的生物信息学管道,我们描述了甲型流感病毒感染过程中人类上皮细胞中 A 到 I 和 C 到 U 的 RNA 编辑事件的特征。我们的结果显示,不同亚型的甲型流感病毒感染可引起人类上皮细胞中 A 到 I RNA 编辑活性的惊人多样性。H1N1 和 H3N2 的感染显着上调了人类上皮细胞中 A 到 I RNA 编辑的归一化水平,而 H5N1 的感染则没有改变,H7N9 的感染则显着下调了 A549 细胞中 A 到 I 编辑的归一化水平。接下来,检查了在病毒感染过程中负责 A 到 I 和 C 到 U RNA 编辑的 ADAR 和 APOBEC 酶的表达水平。一些甲型流感病毒(H1N1 和 H3N2)感染中 A 到 I RNA 编辑活性的增加与 ADAR1 的上调有关,但与 ADAR2 无关。此外,还检查了感染 H1N1、H3N2、H5N1 和 H7N9 的人类上皮细胞的模式识别受体。RIG-I 样受体和 Toll 样受体的基因表达观察到可变的响应变化。最后,还分析了甲型流感病毒感染对禽类宿主中细胞 RNA 编辑活性的影响。

结论

这项工作代表了对人类和禽类宿主中不同甲型流感病毒感染的细胞 RNA 编辑活性的首次全面研究,突出了 RNA 编辑在固有免疫反应和不同亚型甲型流感病毒的致病性中的关键作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aede/5780764/fd50deaabe76/12864_2017_4330_Fig1_HTML.jpg

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