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SARS-CoV-2 亚基因组景观及其新型调控特征。

The SARS-CoV-2 subgenome landscape and its novel regulatory features.

机构信息

State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University, Wuhan, China; Frontier Science Center for Immunology and Metabolism, Wuhan University, Wuhan, China.

State Key Laboratory of Virology, Modern Virology Research Center, College of Life Sciences, Wuhan University, Wuhan, China.

出版信息

Mol Cell. 2021 May 20;81(10):2135-2147.e5. doi: 10.1016/j.molcel.2021.02.036. Epub 2021 Mar 3.

DOI:10.1016/j.molcel.2021.02.036
PMID:33713597
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7927579/
Abstract

Coronavirus disease 2019 (COVID-19), caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), is currently a global pandemic. CoVs are known to generate negative subgenomes (subgenomic RNAs [sgRNAs]) through transcription-regulating sequence (TRS)-dependent template switching, but the global dynamic landscapes of coronaviral subgenomes and regulatory rules remain unclear. Here, using next-generation sequencing (NGS) short-read and Nanopore long-read poly(A) RNA sequencing in two cell types at multiple time points after infection with SARS-CoV-2, we identified hundreds of template switches and constructed the dynamic landscapes of SARS-CoV-2 subgenomes. Interestingly, template switching could occur in a bidirectional manner, with diverse SARS-CoV-2 subgenomes generated from successive template-switching events. The majority of template switches result from RNA-RNA interactions, including seed and compensatory modes, with terminal pairing status as a key determinant. Two TRS-independent template switch modes are also responsible for subgenome biogenesis. Our findings reveal the subgenome landscape of SARS-CoV-2 and its regulatory features, providing a molecular basis for understanding subgenome biogenesis and developing novel anti-viral strategies.

摘要

新型冠状病毒病 2019(COVID-19)由严重急性呼吸综合征冠状病毒 2(SARS-CoV-2)引起,目前已在全球范围内流行。已知冠状病毒通过转录调节序列(TRS)依赖性模板转换产生负亚基因组(亚基因组 RNA[sgRNA]),但冠状病毒亚基因组的全球动态景观和调控规则仍不清楚。在这里,我们使用下一代测序(NGS)短读长和纳米孔长读长 poly(A) RNA 测序,在感染 SARS-CoV-2 后两种细胞类型的多个时间点,鉴定了数百个模板转换,并构建了 SARS-CoV-2 亚基因组的动态景观。有趣的是,模板转换可以双向发生,从连续的模板转换事件中产生了多种 SARS-CoV-2 亚基因组。大多数模板转换是由 RNA-RNA 相互作用引起的,包括种子和补偿模式,末端配对状态是一个关键决定因素。两种 TRS 独立的模板转换模式也负责亚基因组的生物发生。我们的研究结果揭示了 SARS-CoV-2 的亚基因组景观及其调控特征,为理解亚基因组生物发生和开发新型抗病毒策略提供了分子基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4e2/7927579/36044ad1c77a/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4e2/7927579/51ee5102631e/fx1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4e2/7927579/455338768412/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4e2/7927579/a779f4b7ae8e/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4e2/7927579/abe738cc935d/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4e2/7927579/fe61fcd2730a/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4e2/7927579/36044ad1c77a/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4e2/7927579/51ee5102631e/fx1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4e2/7927579/455338768412/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4e2/7927579/a779f4b7ae8e/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4e2/7927579/abe738cc935d/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4e2/7927579/fe61fcd2730a/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e4e2/7927579/36044ad1c77a/gr5_lrg.jpg

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