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Mutation in position of 32 (G>U) of S2M differentiate human SARS-CoV2 from Bat Coronavirus

Majid Vahed, Mohammad Vahed, Aaron Sweeney, Farshad H Shirazi, View ORCID ProfileMehdi Mirsaeidi
doi: https://doi.org/10.1101/2020.09.02.280529
Majid Vahed
1Pharmaceutical Sciences Research Center, Shahid Beheshti University of Medical Sciences, Niayesh Highway, Valiasr Ave, Tehran, Iran
2Department of Toxicology/Pharmacology, School of Pharmacy, Shahid Beheshti, University of Medical Sciences, Niayesh Highway, Valiasr Ave, Tehran, Iran
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Mohammad Vahed
3Department of Computational Medicine and Bioinformatics, University of Michigan, Ann Arbor, MI, 48105, USA
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Aaron Sweeney
4Department of Medicine, School of Medicine, McGill University, Montreal, Quebec, Canada
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Farshad H Shirazi
1Pharmaceutical Sciences Research Center, Shahid Beheshti University of Medical Sciences, Niayesh Highway, Valiasr Ave, Tehran, Iran
2Department of Toxicology/Pharmacology, School of Pharmacy, Shahid Beheshti, University of Medical Sciences, Niayesh Highway, Valiasr Ave, Tehran, Iran
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Mehdi Mirsaeidi
5Division of Pulmonary, Critical Care, Sleep and Allergy, Department of Medicine, Miller School of Medicine, University of Miami, Miami, FL, United States
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  • ORCID record for Mehdi Mirsaeidi
  • For correspondence: msm249@med.miami.edu
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ABSTRACT

The new Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is a zoonotic pathogen that has rapidly mutated and become transmissible to humans. There is little existing data on the mutations in SARS-CoV-2 and the impact of these polymorphisms on its transmission and viral load. In this study, the SARS-CoV-2 genomic sequence was analyzed to identify variants within the 3’UTR region of its cis-regulatory RNA elements. A 43-nucleotide genetic element with a highly conserved stem-loop II-like motif (S2M), was discovered. The research revealed 32 G>U and 16 G>U/A mutations located within the S2M sequence in human SARS-CoV-2 models. These polymorphisms appear to make the S2M secondary and tertiary structures in human SARS-CoV-2 models less stable when compared to the S2M structures of bat/pangolin models. This grants the RNA structures more flexibility, which could be one of its escape mechanisms from host defenses or facilitate its entry into host proteins and enzymes. While this S2M sequence may not be omnipresent across all human SARS-CoV-2 models, when present, its sequence is always highly conserved. It may be used as a potential target for the development of vaccines and therapeutic agents.

Copyright 
The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. This article is a US Government work. It is not subject to copyright under 17 USC 105 and is also made available for use under a CC0 license.
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Posted September 03, 2020.
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Mutation in position of 32 (G>U) of S2M differentiate human SARS-CoV2 from Bat Coronavirus
Majid Vahed, Mohammad Vahed, Aaron Sweeney, Farshad H Shirazi, Mehdi Mirsaeidi
bioRxiv 2020.09.02.280529; doi: https://doi.org/10.1101/2020.09.02.280529
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Mutation in position of 32 (G>U) of S2M differentiate human SARS-CoV2 from Bat Coronavirus
Majid Vahed, Mohammad Vahed, Aaron Sweeney, Farshad H Shirazi, Mehdi Mirsaeidi
bioRxiv 2020.09.02.280529; doi: https://doi.org/10.1101/2020.09.02.280529

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