Cargando…
RNA-induced liquid phase separation of SARS-CoV-2 nucleocapsid protein facilitates NF-κB hyper-activation and inflammation
The ongoing 2019 novel coronavirus disease (COVID-19) caused by SARS-CoV-2 has posed a worldwide pandemic and a major global public health threat. The severity and mortality of COVID-19 are associated with virus-induced dysfunctional inflammatory responses and cytokine storms. However, the interplay...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8065320/ https://www.ncbi.nlm.nih.gov/pubmed/33895773 http://dx.doi.org/10.1038/s41392-021-00575-7 |
_version_ | 1783682315255283712 |
---|---|
author | Wu, Yaoxing Ma, Ling Cai, Sihui Zhuang, Zhen Zhao, Zhiyao Jin, Shouheng Xie, Weihong Zhou, Lingli Zhang, Lei Zhao, Jincun Cui, Jun |
author_facet | Wu, Yaoxing Ma, Ling Cai, Sihui Zhuang, Zhen Zhao, Zhiyao Jin, Shouheng Xie, Weihong Zhou, Lingli Zhang, Lei Zhao, Jincun Cui, Jun |
author_sort | Wu, Yaoxing |
collection | PubMed |
description | The ongoing 2019 novel coronavirus disease (COVID-19) caused by SARS-CoV-2 has posed a worldwide pandemic and a major global public health threat. The severity and mortality of COVID-19 are associated with virus-induced dysfunctional inflammatory responses and cytokine storms. However, the interplay between host inflammatory responses and SARS-CoV-2 infection remains largely unknown. Here, we demonstrate that SARS-CoV-2 nucleocapsid (N) protein, the major structural protein of the virion, promotes the virus-triggered activation of NF-κB signaling. After binding to viral RNA, N protein robustly undergoes liquid–liquid phase separation (LLPS), which recruits TAK1 and IKK complex, the key kinases of NF-κB signaling, to enhance NF-κB activation. Moreover, 1,6-hexanediol, the inhibitor of LLPS, can attenuate the phase separation of N protein and restrict its regulatory functions in NF-κB activation. These results suggest that LLPS of N protein provides a platform to induce NF-κB hyper-activation, which could be a potential therapeutic target against COVID-19 severe pneumonia. |
format | Online Article Text |
id | pubmed-8065320 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-80653202021-04-26 RNA-induced liquid phase separation of SARS-CoV-2 nucleocapsid protein facilitates NF-κB hyper-activation and inflammation Wu, Yaoxing Ma, Ling Cai, Sihui Zhuang, Zhen Zhao, Zhiyao Jin, Shouheng Xie, Weihong Zhou, Lingli Zhang, Lei Zhao, Jincun Cui, Jun Signal Transduct Target Ther Article The ongoing 2019 novel coronavirus disease (COVID-19) caused by SARS-CoV-2 has posed a worldwide pandemic and a major global public health threat. The severity and mortality of COVID-19 are associated with virus-induced dysfunctional inflammatory responses and cytokine storms. However, the interplay between host inflammatory responses and SARS-CoV-2 infection remains largely unknown. Here, we demonstrate that SARS-CoV-2 nucleocapsid (N) protein, the major structural protein of the virion, promotes the virus-triggered activation of NF-κB signaling. After binding to viral RNA, N protein robustly undergoes liquid–liquid phase separation (LLPS), which recruits TAK1 and IKK complex, the key kinases of NF-κB signaling, to enhance NF-κB activation. Moreover, 1,6-hexanediol, the inhibitor of LLPS, can attenuate the phase separation of N protein and restrict its regulatory functions in NF-κB activation. These results suggest that LLPS of N protein provides a platform to induce NF-κB hyper-activation, which could be a potential therapeutic target against COVID-19 severe pneumonia. Nature Publishing Group UK 2021-04-24 /pmc/articles/PMC8065320/ /pubmed/33895773 http://dx.doi.org/10.1038/s41392-021-00575-7 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Wu, Yaoxing Ma, Ling Cai, Sihui Zhuang, Zhen Zhao, Zhiyao Jin, Shouheng Xie, Weihong Zhou, Lingli Zhang, Lei Zhao, Jincun Cui, Jun RNA-induced liquid phase separation of SARS-CoV-2 nucleocapsid protein facilitates NF-κB hyper-activation and inflammation |
title | RNA-induced liquid phase separation of SARS-CoV-2 nucleocapsid protein facilitates NF-κB hyper-activation and inflammation |
title_full | RNA-induced liquid phase separation of SARS-CoV-2 nucleocapsid protein facilitates NF-κB hyper-activation and inflammation |
title_fullStr | RNA-induced liquid phase separation of SARS-CoV-2 nucleocapsid protein facilitates NF-κB hyper-activation and inflammation |
title_full_unstemmed | RNA-induced liquid phase separation of SARS-CoV-2 nucleocapsid protein facilitates NF-κB hyper-activation and inflammation |
title_short | RNA-induced liquid phase separation of SARS-CoV-2 nucleocapsid protein facilitates NF-κB hyper-activation and inflammation |
title_sort | rna-induced liquid phase separation of sars-cov-2 nucleocapsid protein facilitates nf-κb hyper-activation and inflammation |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8065320/ https://www.ncbi.nlm.nih.gov/pubmed/33895773 http://dx.doi.org/10.1038/s41392-021-00575-7 |
work_keys_str_mv | AT wuyaoxing rnainducedliquidphaseseparationofsarscov2nucleocapsidproteinfacilitatesnfkbhyperactivationandinflammation AT maling rnainducedliquidphaseseparationofsarscov2nucleocapsidproteinfacilitatesnfkbhyperactivationandinflammation AT caisihui rnainducedliquidphaseseparationofsarscov2nucleocapsidproteinfacilitatesnfkbhyperactivationandinflammation AT zhuangzhen rnainducedliquidphaseseparationofsarscov2nucleocapsidproteinfacilitatesnfkbhyperactivationandinflammation AT zhaozhiyao rnainducedliquidphaseseparationofsarscov2nucleocapsidproteinfacilitatesnfkbhyperactivationandinflammation AT jinshouheng rnainducedliquidphaseseparationofsarscov2nucleocapsidproteinfacilitatesnfkbhyperactivationandinflammation AT xieweihong rnainducedliquidphaseseparationofsarscov2nucleocapsidproteinfacilitatesnfkbhyperactivationandinflammation AT zhoulingli rnainducedliquidphaseseparationofsarscov2nucleocapsidproteinfacilitatesnfkbhyperactivationandinflammation AT zhanglei rnainducedliquidphaseseparationofsarscov2nucleocapsidproteinfacilitatesnfkbhyperactivationandinflammation AT zhaojincun rnainducedliquidphaseseparationofsarscov2nucleocapsidproteinfacilitatesnfkbhyperactivationandinflammation AT cuijun rnainducedliquidphaseseparationofsarscov2nucleocapsidproteinfacilitatesnfkbhyperactivationandinflammation |