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Tytuł:
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IL6-mediated HCoV-host interactome regulatory network and GO/Pathway enrichment analysis.
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Autorzy:
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Politano G; Computer Science and Automation Department, Politecnico di Torino, Italy.
Benso A; Computer Science and Automation Department, Politecnico di Torino, Italy.
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Źródło:
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PLoS computational biology [PLoS Comput Biol] 2020 Sep 30; Vol. 16 (9), pp. e1008238. Date of Electronic Publication: 2020 Sep 30 (Print Publication: 2020).
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Typ publikacji:
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Journal Article
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Język:
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English
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Imprint Name(s):
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Original Publication: San Francisco, CA : Public Library of Science, [2005]-
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MeSH Terms:
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Gene Ontology*
Host-Pathogen Interactions*
Betacoronavirus/*physiology
Coronavirus Infections/*virology
Interleukin-6/*physiology
Pneumonia, Viral/*virology
Betacoronavirus/genetics ; COVID-19 ; Genes, Viral ; Humans ; Pandemics ; SARS-CoV-2 ; Viral Proteins/genetics ; Viral Proteins/physiology
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Substance Nomenclature:
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0 (IL6 protein, human)
0 (Interleukin-6)
0 (Viral Proteins)
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Entry Date(s):
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Date Created: 20200930 Date Completed: 20201027 Latest Revision: 20231104
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Update Code:
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20240105
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PubMed Central ID:
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PMC7561109
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DOI:
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10.1371/journal.pcbi.1008238
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PMID:
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32997660
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During these days of global emergency for the COVID-19 disease outbreak, there is an urgency to share reliable information able to help worldwide life scientists to get better insights and make sense of the large amount of data currently available. In this study we used the results presented in [1] to perform two different Systems Biology analyses on the HCoV-host interactome. In the first one, we reconstructed the interactome of the HCoV-host proteins, integrating it with highly reliable miRNA and drug interactions information. We then added the IL-6 gene, identified in recent publications [2] as heavily involved in the COVID-19 progression and, interestingly, we identified several interactions with the reconstructed interactome. In the second analysis, we performed a Gene Ontology and a Pathways enrichment analysis on the full set of the HCoV-host interactome proteins and on the ones belonging to a significantly dense cluster of interacting proteins identified in the first analysis. Results of the two analyses provide a compact but comprehensive glance on some of the current state-of-the-art regulations, GO, and pathways involved in the HCoV-host interactome, and that could support all scientists currently focusing on SARS-CoV-2 research.
Competing Interests: The authors have declared that no competing interests exist.
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