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Evidence for host-dependent RNA editing in the transcriptome of SARS-CoV-2

机译:SARS-COV-2转录组中宿主依赖性RNA编辑的证据

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The COVID-19 outbreak has become a global health risk, and understanding the response of the host to the SARS-CoV-2 virus will help to combat the disease. RNA editing by host deaminases is an innate restriction process to counter virus infection, but it is not yet known whether this process operates against coronaviruses. Here, we analyze RNA sequences from bronchoalveolar lavage fluids obtained from coronavirus-infected patients. We identify nucleotide changes that may be signatures of RNA editing: adenosine-to-inosine changes from ADAR deaminases and cytosine-to-uracil changes from APOBEC deaminases. Mutational analysis of genomes from different strains of Coronaviridae from human hosts reveals mutational patterns consistent with those observed in the transcriptomic data. However, the reduced ADAR signature in these data raises the possibility that ADARs might be more effective than APOBECs in restricting viral propagation. Our results thus suggest that both APOBECs and ADARs are involved in coronavirus genome editing, a process that may shape the fate of both virus and patient.
机译:Covid-19爆发已成为全球性健康风险,并了解宿主对SARS-COV-2病毒的反应将有助于打击这种疾病。通过宿主脱胺酶进行RNA编辑是对反病毒感染的先天限制过程,但尚不了解该过程是否对冠状病毒进行操作。在此,我们分析从冠状病毒感染患者获得的支气管肺泡灌洗液中的RNA序列。我们鉴定可能是RNA编辑特征的核苷酸变化:从ADAR脱氨酶和胞嘧啶与尿嘧啶的腺苷与尿嘧啶从Apobec deaminase的变化发生变化。来自人宿主的不同菌株菌株的基因组的突变分析揭示了与在转录组数据中观察到的那些一致的突变模式。然而,这些数据中的减少的ADAR签名提出了在限制病毒传播时,ADARS可能比apobec更有效的可能性。因此,我们的结果表明,Apobecs和Adars都参与了冠状病毒基因组编辑,这是一种可以塑造病毒和患者的命运的过程。

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