This article was originally published here<\/p>\n
Mol Cell. 2021 Jan 1:S1097-2765(20)30962-X. doi: 10.1016\/j.molcel.2020.12.041. Online ahead of print.<\/p>\n
ABSTRACT<\/p>\n
Severe-acute-respiratory-syndrome-related coronavirus 2 (SARS-CoV-2) is the positive-sense RNA virus that causes coronavirus disease 2019 (COVID-19). The genome of SARS-CoV-2 is unique among viral RNAs in its vast potential to form RNA structures, yet as much as 97% of its 30 kilobases have not been structurally explored. Here, we apply a novel long amplicon strategy to determine the secondary structure of the SARS-CoV-2 RNA genome at single-nucleotide resolution in infected cells. Our in-depth structural analysis reveals networks of well-folded RNA structures throughout Orf1ab and reveals aspects of SARS-CoV-2 genome architecture that distinguish it from other RNA viruses. Evolutionary analysis shows that several features of the SARS-CoV-2 genomic structure are conserved across -coronaviruses, and we pinpoint regions of well-folded RNA structure that merit downstream functional analysis. The native, secondary structure of SARS-CoV-2 presented here is a roadmap that will facilitate focused studies on the viral life cycle, facilitate primer design, and guide the identification of RNA drug targets against COVID-19.<\/p>\n
PMID:33444546 | DOI:10.1016\/j.molcel.2020.12.041<\/p>\n
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See the article here: This article was originally published here Mol Cell. 2021 Jan 1:S1097-2765(20)30962-X. doi: 10.1016\/j.molcel.2020.12.041 Continue reading
\nComprehensive in vivo secondary structure of the SARS-CoV-2 genome reveals novel regulatory motifs and mechanisms - DocWire News<\/a><\/p>\n","protected":false},"excerpt":{"rendered":"