Dynamic changes in gene-to-gene regulatory networks in response to SARS-CoV-2 infection
Abstract The current pandemic of SARS-CoV-2 has caused extensive damage to society. The characterization of SARS-CoV-2 profiles has been addressed by researchers globally with the aim of resolving this disruptive crisis. This investigation process is indispensable to understand how SARS-CoV-2 behave...
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2021-05-01
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Online Access: | https://doi.org/10.1038/s41598-021-90556-1 |
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doaj-5fe2c81e065e4d34a240b474c1d2a8fb2021-05-30T11:35:15ZengNature Publishing GroupScientific Reports2045-23222021-05-0111111310.1038/s41598-021-90556-1Dynamic changes in gene-to-gene regulatory networks in response to SARS-CoV-2 infectionYoshihisa Tanaka0Kako Higashihara1Mai Adachi Nakazawa2Fumiyoshi Yamashita3Yoshinori Tamada4Yasushi Okuno5Graduate School of Pharmaceutical Sciences, Kyoto UniversityGraduate School of Medicine, Kyoto UniversityGraduate School of Medicine, Kyoto UniversityGraduate School of Pharmaceutical Sciences, Kyoto UniversityGraduate School of Medicine, Kyoto UniversityBiomedical Computational Intelligence Unit, HPC- and AI-driven Drug Development Platform Division, RIKEN Center for Computational ScienceAbstract The current pandemic of SARS-CoV-2 has caused extensive damage to society. The characterization of SARS-CoV-2 profiles has been addressed by researchers globally with the aim of resolving this disruptive crisis. This investigation process is indispensable to understand how SARS-CoV-2 behaves in human host cells. However, little is known about the systematic molecular mechanisms involved in the effects of SARS-CoV-2 infection on human host cells. Here, we present gene-to-gene regulatory networks in response to SARS-CoV-2 using a Bayesian network. We examined the dynamic changes in the SARS-CoV-2-purturbated networks established by our proposed framework for gene network analysis, thus revealing that interferon signaling gradually switched to the subsequent inflammatory cytokine signaling cascades. Furthermore, we succeeded in capturing a COVID-19 patient-specific network in which transduction of these signals was concurrently induced. This enabled us to explore the local regulatory systems influenced by SARS-CoV-2 in host cells more precisely at an individual level. Our panel of network analyses has provided new insights into SARS-CoV-2 research from the perspective of cellular systems.https://doi.org/10.1038/s41598-021-90556-1 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yoshihisa Tanaka Kako Higashihara Mai Adachi Nakazawa Fumiyoshi Yamashita Yoshinori Tamada Yasushi Okuno |
spellingShingle |
Yoshihisa Tanaka Kako Higashihara Mai Adachi Nakazawa Fumiyoshi Yamashita Yoshinori Tamada Yasushi Okuno Dynamic changes in gene-to-gene regulatory networks in response to SARS-CoV-2 infection Scientific Reports |
author_facet |
Yoshihisa Tanaka Kako Higashihara Mai Adachi Nakazawa Fumiyoshi Yamashita Yoshinori Tamada Yasushi Okuno |
author_sort |
Yoshihisa Tanaka |
title |
Dynamic changes in gene-to-gene regulatory networks in response to SARS-CoV-2 infection |
title_short |
Dynamic changes in gene-to-gene regulatory networks in response to SARS-CoV-2 infection |
title_full |
Dynamic changes in gene-to-gene regulatory networks in response to SARS-CoV-2 infection |
title_fullStr |
Dynamic changes in gene-to-gene regulatory networks in response to SARS-CoV-2 infection |
title_full_unstemmed |
Dynamic changes in gene-to-gene regulatory networks in response to SARS-CoV-2 infection |
title_sort |
dynamic changes in gene-to-gene regulatory networks in response to sars-cov-2 infection |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2021-05-01 |
description |
Abstract The current pandemic of SARS-CoV-2 has caused extensive damage to society. The characterization of SARS-CoV-2 profiles has been addressed by researchers globally with the aim of resolving this disruptive crisis. This investigation process is indispensable to understand how SARS-CoV-2 behaves in human host cells. However, little is known about the systematic molecular mechanisms involved in the effects of SARS-CoV-2 infection on human host cells. Here, we present gene-to-gene regulatory networks in response to SARS-CoV-2 using a Bayesian network. We examined the dynamic changes in the SARS-CoV-2-purturbated networks established by our proposed framework for gene network analysis, thus revealing that interferon signaling gradually switched to the subsequent inflammatory cytokine signaling cascades. Furthermore, we succeeded in capturing a COVID-19 patient-specific network in which transduction of these signals was concurrently induced. This enabled us to explore the local regulatory systems influenced by SARS-CoV-2 in host cells more precisely at an individual level. Our panel of network analyses has provided new insights into SARS-CoV-2 research from the perspective of cellular systems. |
url |
https://doi.org/10.1038/s41598-021-90556-1 |
work_keys_str_mv |
AT yoshihisatanaka dynamicchangesingenetogeneregulatorynetworksinresponsetosarscov2infection AT kakohigashihara dynamicchangesingenetogeneregulatorynetworksinresponsetosarscov2infection AT maiadachinakazawa dynamicchangesingenetogeneregulatorynetworksinresponsetosarscov2infection AT fumiyoshiyamashita dynamicchangesingenetogeneregulatorynetworksinresponsetosarscov2infection AT yoshinoritamada dynamicchangesingenetogeneregulatorynetworksinresponsetosarscov2infection AT yasushiokuno dynamicchangesingenetogeneregulatorynetworksinresponsetosarscov2infection |
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