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Alternative splicing of OAS1 alters the risk for severe COVID-19
A locus containing OAS1/2/3 has been identified as a risk locus for severe COVID-19 among Europeans ancestry individuals, with a protective haplotype of ~75 kilobases derived from Neanderthals. Here, we show that among several potentially causal variants at this locus, a splice variant of OAS1 occur...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8010745/ https://www.ncbi.nlm.nih.gov/pubmed/33791713 http://dx.doi.org/10.1101/2021.03.20.21254005 |
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author | Huffman, Jennifer Butler-Laporte, Guillaume Khan, Atlas Drivas, Theodore G. Peloso, Gina M. Nakanishi, Tomoko Verma, Anurag Kiryluk, Krzysztof Richards, J. Brent Zeberg, Hugo |
author_facet | Huffman, Jennifer Butler-Laporte, Guillaume Khan, Atlas Drivas, Theodore G. Peloso, Gina M. Nakanishi, Tomoko Verma, Anurag Kiryluk, Krzysztof Richards, J. Brent Zeberg, Hugo |
author_sort | Huffman, Jennifer |
collection | PubMed |
description | A locus containing OAS1/2/3 has been identified as a risk locus for severe COVID-19 among Europeans ancestry individuals, with a protective haplotype of ~75 kilobases derived from Neanderthals. Here, we show that among several potentially causal variants at this locus, a splice variant of OAS1 occurs in people of African ancestry independently of the Neanderthal haplotype and confers protection against COVID-19 of a magnitude similar to that seen in individuals without African ancestry. |
format | Online Article Text |
id | pubmed-8010745 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-80107452021-04-01 Alternative splicing of OAS1 alters the risk for severe COVID-19 Huffman, Jennifer Butler-Laporte, Guillaume Khan, Atlas Drivas, Theodore G. Peloso, Gina M. Nakanishi, Tomoko Verma, Anurag Kiryluk, Krzysztof Richards, J. Brent Zeberg, Hugo medRxiv Article A locus containing OAS1/2/3 has been identified as a risk locus for severe COVID-19 among Europeans ancestry individuals, with a protective haplotype of ~75 kilobases derived from Neanderthals. Here, we show that among several potentially causal variants at this locus, a splice variant of OAS1 occurs in people of African ancestry independently of the Neanderthal haplotype and confers protection against COVID-19 of a magnitude similar to that seen in individuals without African ancestry. Cold Spring Harbor Laboratory 2021-03-25 /pmc/articles/PMC8010745/ /pubmed/33791713 http://dx.doi.org/10.1101/2021.03.20.21254005 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Huffman, Jennifer Butler-Laporte, Guillaume Khan, Atlas Drivas, Theodore G. Peloso, Gina M. Nakanishi, Tomoko Verma, Anurag Kiryluk, Krzysztof Richards, J. Brent Zeberg, Hugo Alternative splicing of OAS1 alters the risk for severe COVID-19 |
title | Alternative splicing of OAS1 alters the risk for severe COVID-19 |
title_full | Alternative splicing of OAS1 alters the risk for severe COVID-19 |
title_fullStr | Alternative splicing of OAS1 alters the risk for severe COVID-19 |
title_full_unstemmed | Alternative splicing of OAS1 alters the risk for severe COVID-19 |
title_short | Alternative splicing of OAS1 alters the risk for severe COVID-19 |
title_sort | alternative splicing of oas1 alters the risk for severe covid-19 |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8010745/ https://www.ncbi.nlm.nih.gov/pubmed/33791713 http://dx.doi.org/10.1101/2021.03.20.21254005 |
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