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

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...

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Detalles Bibliográficos
Autores principales: Wang, Dehe, Jiang, Ao, Feng, Jiangpeng, Li, Guangnan, Guo, Dong, Sajid, Muhammad, Wu, Kai, Zhang, Qiuhan, Ponty, Yann, Will, Sebastian, Liu, Feiyan, Yu, Xinghai, Li, Shaopeng, Liu, Qianyun, Yang, Xing-Lou, Guo, Ming, Li, Xingqiao, Chen, Mingzhou, Shi, Zheng-Li, Lan, Ke, Chen, Yu, Zhou, Yu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7927579/
https://www.ncbi.nlm.nih.gov/pubmed/33713597
http://dx.doi.org/10.1016/j.molcel.2021.02.036
Descripción
Sumario: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.