miRNA binding pressure channels evolution of SARS-CoV-2 genomes
A. Zhiyanov, M. Shkurnikov, A. Nersisyan, H. Cai, A. Baranova, A. Tonevitsky
Abstract
In somatic cells, microRNAs (miRNAs) bind to the genomes of RNA viruses and influence their translation and replication. Here we demonstrate that a significant number of miRNA binding sites locate in the NSP4 region of the SARS-CoV-2 genome, and the intestinal human miRNAs exert evolutionary pressure on this region. Notably, in infected cells, NSP4 promotes the formation of double-membrane vesicles, which serve as the scaffolds for replication-transcriptional complexes and protect viral RNA from intracellular destruction. In three years of selection, the loss of many miRNA binding sites, in particular, those within the NSP4, has shaped the SARS-CoV-2 genomes to promote the descendants of the BA.2 variants as the dominant strains and define current momentum of the pandemics.
02 /Specification & Classification
Click any tag to browse matching papers- Organism
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Implications of SARS-CoV-2 mutations for genomic RNA structure and host microRNA targeting
Seyed Mohammad Ali Hosseini Rad, Alexander Donald McLellan·International Journal of Molecular SciencesPeer-reviewed·Jul 7, 2020
- SARS-CoV-2 mutations altering regulatory properties: deciphering host's and virus's perspectives
Abul Bashar Mir Md. Khademul Islam, Md. Abdullah‐Al‐Kamran Khan·Gene ReportsPeer-reviewed·Jun 11, 2021
- Antiviral effects of miRNAs in extracellular vesicles against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and mutations in SARS-CoV-2 RNA virus
Jae Hyeon Park, Yuri Choi, … Jisook Moon·bioRxiv·Jul 27, 2020
- In-silico analysis of SARS-CoV-2 genomes: Insights from SARS encoded non-coding RNAs
N. Periwal, S. Sarma, … V. Sood·bioRxiv·Mar 31, 2020
- Conserved Genomic Terminals of SARS-CoV-2 as Co-evolving Functional Elements and Potential Therapeutic Targets
Agnes Pui-Yee Chan, Yongwook Choi, Nicholas J. Schork·mSpherePeer-reviewed·Dec 1, 2020
- Host microRNA interactions with the SARS-CoV-2 viral genome 3'-untranslated region
C. J. Frye, C. L. Cunningham, M. R. Mihailescu·bioRxiv·May 18, 2023