tetano
Editor, Senior Moderator
J Biol Chem
. 2022 Jan 12;101584.
doi: 10.1016/j.jbc.2022.101584. Online ahead of print.
Host E3 ligase HUWE1 attenuates the pro-apoptotic activity of the MERS-CoV accessory protein ORF3 by promoting its ubiquitin-dependent degradation
Yuzheng Zhou[SUP] 1 [/SUP], Rong Zheng[SUP] 1 [/SUP], Sixu Liu[SUP] 1 [/SUP], Cyrollah Disoma[SUP] 1 [/SUP], Ashuai Du[SUP] 1 [/SUP], Shiqin Li[SUP] 1 [/SUP], Zongpeng Chen[SUP] 1 [/SUP], Zijun Dong[SUP] 2 [/SUP], Yongxing Zhang[SUP] 1 [/SUP], Sijia Li[SUP] 1 [/SUP], Pinjia Liu[SUP] 1 [/SUP], Aroona Razzaq[SUP] 1 [/SUP], Xuan Chen[SUP] 1 [/SUP], Yujie Liao[SUP] 1 [/SUP], Siyi Tao[SUP] 1 [/SUP], Yuxin Liu[SUP] 1 [/SUP], Lunan Xu[SUP] 1 [/SUP], Qianjun Zhang[SUP] 3 [/SUP], Jian Peng[SUP] 4 [/SUP], Xu Deng[SUP] 5 [/SUP], Shanni Li[SUP] 1 [/SUP], Taijiao Jiang[SUP] 6 [/SUP], Zanxian Xia[SUP] 7 [/SUP]
Affiliations
Abstract
With the outbreak of SARS-CoV-2, coronaviruses have begun to attract great attention across the world. Of the known human coronaviruses, however, MERS-CoV is the most lethal. Coronavirus proteins can be divided into three groups: nonstructural proteins, structural proteins, and accessory proteins. While the number of each of these proteins varies greatly among different coronaviruses, accessory proteins are most closely related to the pathogenicity of the virus. We found for the first time that the ORF3 accessory protein of MERS-CoV, which closely resembles the ORF3a proteins of SARS-CoV and SARS-CoV-2, has the ability to induce apoptosis in cells in a dose-dependent manner. Although the functions of these three proteins are similar, the amino acid sequences and structures differ. Through bioinformatics analysis and validation, we revealed that ORF3 is an unstable protein, and has a shorter half-life in cells compared to that of SARS-CoV and SARS-CoV-2 ORF3a proteins. After screening, we identified a host E3 ligase, HUWE1, that specifically induces MERS-CoV ORF3 protein ubiquitination and degradation through the ubiquitin proteasome system. This results in the diminished ability of ORF3 to induce apoptosis, which might partially explain the lower spread of MERS-CoV compared to other coronaviruses. In summary, this study reveals a pathological function of MERS-CoV ORF3 protein and identifies a potential host antiviral protein, HUWE1, with an ability to antagonize MERS-CoV pathogenesis by inducing ORF3 degradation, thus enriching our knowledge of the pathogenesis of MERS-CoV and suggesting new targets and strategies for clinical development of drugs for MERS-CoV treatment.
Keywords: HUWE1; MERS-CoV; ORF3; apoptosis; degradation; ubiquitination.
. 2022 Jan 12;101584.
doi: 10.1016/j.jbc.2022.101584. Online ahead of print.
Host E3 ligase HUWE1 attenuates the pro-apoptotic activity of the MERS-CoV accessory protein ORF3 by promoting its ubiquitin-dependent degradation
Yuzheng Zhou[SUP] 1 [/SUP], Rong Zheng[SUP] 1 [/SUP], Sixu Liu[SUP] 1 [/SUP], Cyrollah Disoma[SUP] 1 [/SUP], Ashuai Du[SUP] 1 [/SUP], Shiqin Li[SUP] 1 [/SUP], Zongpeng Chen[SUP] 1 [/SUP], Zijun Dong[SUP] 2 [/SUP], Yongxing Zhang[SUP] 1 [/SUP], Sijia Li[SUP] 1 [/SUP], Pinjia Liu[SUP] 1 [/SUP], Aroona Razzaq[SUP] 1 [/SUP], Xuan Chen[SUP] 1 [/SUP], Yujie Liao[SUP] 1 [/SUP], Siyi Tao[SUP] 1 [/SUP], Yuxin Liu[SUP] 1 [/SUP], Lunan Xu[SUP] 1 [/SUP], Qianjun Zhang[SUP] 3 [/SUP], Jian Peng[SUP] 4 [/SUP], Xu Deng[SUP] 5 [/SUP], Shanni Li[SUP] 1 [/SUP], Taijiao Jiang[SUP] 6 [/SUP], Zanxian Xia[SUP] 7 [/SUP]
Affiliations
- PMID: 35032548
- PMCID: PMC8755419
- DOI: 10.1016/j.jbc.2022.101584
Abstract
With the outbreak of SARS-CoV-2, coronaviruses have begun to attract great attention across the world. Of the known human coronaviruses, however, MERS-CoV is the most lethal. Coronavirus proteins can be divided into three groups: nonstructural proteins, structural proteins, and accessory proteins. While the number of each of these proteins varies greatly among different coronaviruses, accessory proteins are most closely related to the pathogenicity of the virus. We found for the first time that the ORF3 accessory protein of MERS-CoV, which closely resembles the ORF3a proteins of SARS-CoV and SARS-CoV-2, has the ability to induce apoptosis in cells in a dose-dependent manner. Although the functions of these three proteins are similar, the amino acid sequences and structures differ. Through bioinformatics analysis and validation, we revealed that ORF3 is an unstable protein, and has a shorter half-life in cells compared to that of SARS-CoV and SARS-CoV-2 ORF3a proteins. After screening, we identified a host E3 ligase, HUWE1, that specifically induces MERS-CoV ORF3 protein ubiquitination and degradation through the ubiquitin proteasome system. This results in the diminished ability of ORF3 to induce apoptosis, which might partially explain the lower spread of MERS-CoV compared to other coronaviruses. In summary, this study reveals a pathological function of MERS-CoV ORF3 protein and identifies a potential host antiviral protein, HUWE1, with an ability to antagonize MERS-CoV pathogenesis by inducing ORF3 degradation, thus enriching our knowledge of the pathogenesis of MERS-CoV and suggesting new targets and strategies for clinical development of drugs for MERS-CoV treatment.
Keywords: HUWE1; MERS-CoV; ORF3; apoptosis; degradation; ubiquitination.