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SARS-Cov-2 ORF3a: Mutability and function
In this study, analysis of changes of SARS-CoV-2 ORF3a protein during pandemic is reported. ORF3a, a conserved coronavirus protein, is involved in virus replication and release. A set of 70,752 high-quality SARS-CoV-2 genomes available in GISAID databank at the end of August 2020 have been scanned....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier B.V.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7836370/ https://www.ncbi.nlm.nih.gov/pubmed/33359807 http://dx.doi.org/10.1016/j.ijbiomac.2020.12.142 |
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author | Bianchi, Martina Borsetti, Alessandra Ciccozzi, Massimo Pascarella, Stefano |
author_facet | Bianchi, Martina Borsetti, Alessandra Ciccozzi, Massimo Pascarella, Stefano |
author_sort | Bianchi, Martina |
collection | PubMed |
description | In this study, analysis of changes of SARS-CoV-2 ORF3a protein during pandemic is reported. ORF3a, a conserved coronavirus protein, is involved in virus replication and release. A set of 70,752 high-quality SARS-CoV-2 genomes available in GISAID databank at the end of August 2020 have been scanned. All ORF3a mutations in the virus genomes were grouped according to the collection date interval and over the entire data set. The considered intervals were: start of collection-February, March, April, May, June, July and August 2020. The top five most frequent variants were examined within each collection interval. Overall, seventeen variants have been isolated. Ten of the seventeen mutant sites occur within the transmembrane (TM) domain of ORF3a and are in contact with the central pore or side tunnels. The other variant sites are in different places of the ORF3a structure. Within the entire sample, the five most frequent mutations are V13L, Q57H, Q57H + A99V, G196V and G252V. The same analysis identified 28 sites identically conserved in all the genome isolates. These sites are possibly involved in stabilization of monomer, dimer, tetramerization and interaction with other cellular components. The results here reported can be helpful to understand virus biology and to design new therapeutic strategies. |
format | Online Article Text |
id | pubmed-7836370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Elsevier B.V. |
record_format | MEDLINE/PubMed |
spelling | pubmed-78363702021-01-26 SARS-Cov-2 ORF3a: Mutability and function Bianchi, Martina Borsetti, Alessandra Ciccozzi, Massimo Pascarella, Stefano Int J Biol Macromol Article In this study, analysis of changes of SARS-CoV-2 ORF3a protein during pandemic is reported. ORF3a, a conserved coronavirus protein, is involved in virus replication and release. A set of 70,752 high-quality SARS-CoV-2 genomes available in GISAID databank at the end of August 2020 have been scanned. All ORF3a mutations in the virus genomes were grouped according to the collection date interval and over the entire data set. The considered intervals were: start of collection-February, March, April, May, June, July and August 2020. The top five most frequent variants were examined within each collection interval. Overall, seventeen variants have been isolated. Ten of the seventeen mutant sites occur within the transmembrane (TM) domain of ORF3a and are in contact with the central pore or side tunnels. The other variant sites are in different places of the ORF3a structure. Within the entire sample, the five most frequent mutations are V13L, Q57H, Q57H + A99V, G196V and G252V. The same analysis identified 28 sites identically conserved in all the genome isolates. These sites are possibly involved in stabilization of monomer, dimer, tetramerization and interaction with other cellular components. The results here reported can be helpful to understand virus biology and to design new therapeutic strategies. Elsevier B.V. 2021-02-15 2021-01-08 /pmc/articles/PMC7836370/ /pubmed/33359807 http://dx.doi.org/10.1016/j.ijbiomac.2020.12.142 Text en © 2020 Elsevier B.V. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Bianchi, Martina Borsetti, Alessandra Ciccozzi, Massimo Pascarella, Stefano SARS-Cov-2 ORF3a: Mutability and function |
title | SARS-Cov-2 ORF3a: Mutability and function |
title_full | SARS-Cov-2 ORF3a: Mutability and function |
title_fullStr | SARS-Cov-2 ORF3a: Mutability and function |
title_full_unstemmed | SARS-Cov-2 ORF3a: Mutability and function |
title_short | SARS-Cov-2 ORF3a: Mutability and function |
title_sort | sars-cov-2 orf3a: mutability and function |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7836370/ https://www.ncbi.nlm.nih.gov/pubmed/33359807 http://dx.doi.org/10.1016/j.ijbiomac.2020.12.142 |
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