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GC usage of SARS-CoV-2 genes might adapt to the environment of human lung expressed genes

Understanding how SARS-CoV-2 (Severe Acute Respiratory Syndrome Coronavirus 2) efficiently reproduces itself by taking resources from the human host could facilitate the development of drugs against the virus. SARS-CoV-2 translates its own proteins by using the host tRNAs, so that its GC or codon us...

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Autores principales: Li, Yue, Yang, Xinai, Wang, Na, Wang, Haiyan, Yin, Bin, Yang, Xiaoping, Jiang, Wenqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7473593/
https://www.ncbi.nlm.nih.gov/pubmed/32888056
http://dx.doi.org/10.1007/s00438-020-01719-0
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author Li, Yue
Yang, Xinai
Wang, Na
Wang, Haiyan
Yin, Bin
Yang, Xiaoping
Jiang, Wenqing
author_facet Li, Yue
Yang, Xinai
Wang, Na
Wang, Haiyan
Yin, Bin
Yang, Xiaoping
Jiang, Wenqing
author_sort Li, Yue
collection PubMed
description Understanding how SARS-CoV-2 (Severe Acute Respiratory Syndrome Coronavirus 2) efficiently reproduces itself by taking resources from the human host could facilitate the development of drugs against the virus. SARS-CoV-2 translates its own proteins by using the host tRNAs, so that its GC or codon usage should fit that of the host cells. It is necessary to study both the virus and human genomes in the light of evolution and adaptation. The SARS-CoV-2 virus has significantly lower GC content and GC3 as compared to human. However, when we selected a set of human genes that have similar GC properties to SARS-CoV-2, we found that these genes were enriched in particular pathways. Moreover, these human genes have the codon composition perfectly correlated with the SARS-CoV-2, and were extraordinarily highly expressed in human lung tissues, demonstrating that the SARS-CoV-2 genes have similar GC usage as compared to the lung expressed human genes. RSCU (relative synonymous codon usage) and CAI (codon adaptation index) profiles further support the matching between SARS-CoV-2 and lungs. Our study indicates that SARS-CoV-2 might have adapted to the human lung environment by observing the high correlation between GC usage of SARS-CoV-2 and human lung genes, which suggests the GC content of SARS-CoV-2 is optimized to take advantage of human lung tissues.
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spelling pubmed-74735932020-09-08 GC usage of SARS-CoV-2 genes might adapt to the environment of human lung expressed genes Li, Yue Yang, Xinai Wang, Na Wang, Haiyan Yin, Bin Yang, Xiaoping Jiang, Wenqing Mol Genet Genomics Original Article Understanding how SARS-CoV-2 (Severe Acute Respiratory Syndrome Coronavirus 2) efficiently reproduces itself by taking resources from the human host could facilitate the development of drugs against the virus. SARS-CoV-2 translates its own proteins by using the host tRNAs, so that its GC or codon usage should fit that of the host cells. It is necessary to study both the virus and human genomes in the light of evolution and adaptation. The SARS-CoV-2 virus has significantly lower GC content and GC3 as compared to human. However, when we selected a set of human genes that have similar GC properties to SARS-CoV-2, we found that these genes were enriched in particular pathways. Moreover, these human genes have the codon composition perfectly correlated with the SARS-CoV-2, and were extraordinarily highly expressed in human lung tissues, demonstrating that the SARS-CoV-2 genes have similar GC usage as compared to the lung expressed human genes. RSCU (relative synonymous codon usage) and CAI (codon adaptation index) profiles further support the matching between SARS-CoV-2 and lungs. Our study indicates that SARS-CoV-2 might have adapted to the human lung environment by observing the high correlation between GC usage of SARS-CoV-2 and human lung genes, which suggests the GC content of SARS-CoV-2 is optimized to take advantage of human lung tissues. Springer Berlin Heidelberg 2020-09-04 2020 /pmc/articles/PMC7473593/ /pubmed/32888056 http://dx.doi.org/10.1007/s00438-020-01719-0 Text en © Springer-Verlag GmbH Germany, part of Springer Nature 2020 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Article
Li, Yue
Yang, Xinai
Wang, Na
Wang, Haiyan
Yin, Bin
Yang, Xiaoping
Jiang, Wenqing
GC usage of SARS-CoV-2 genes might adapt to the environment of human lung expressed genes
title GC usage of SARS-CoV-2 genes might adapt to the environment of human lung expressed genes
title_full GC usage of SARS-CoV-2 genes might adapt to the environment of human lung expressed genes
title_fullStr GC usage of SARS-CoV-2 genes might adapt to the environment of human lung expressed genes
title_full_unstemmed GC usage of SARS-CoV-2 genes might adapt to the environment of human lung expressed genes
title_short GC usage of SARS-CoV-2 genes might adapt to the environment of human lung expressed genes
title_sort gc usage of sars-cov-2 genes might adapt to the environment of human lung expressed genes
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7473593/
https://www.ncbi.nlm.nih.gov/pubmed/32888056
http://dx.doi.org/10.1007/s00438-020-01719-0
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