• Media type: E-Article
  • Title: CRL4B E3 ligase recruited by PRPF19 inhibits SARS-CoV-2 infection by targeting ORF6 for ubiquitin-dependent degradation
  • Contributor: Zhang, Linran; Hao, Pengfei; Chen, Xiang; Lv, Shuai; Gao, Wenying; Li, Chang; Li, Zhaolong; Zhang, Wenyan
  • imprint: American Society for Microbiology, 2024
  • Published in: mBio
  • Language: English
  • DOI: 10.1128/mbio.03071-23
  • ISSN: 2150-7511
  • Origination:
  • Footnote:
  • Description: <jats:p>The cellular biological function of the ubiquitin-proteasome pathway as an important modulator for the regulation of many fundamental cellular processes has been greatly appreciated. The critical role of the ubiquitin-proteasome pathway in viral pathogenesis has become increasingly apparent. It is a powerful tool that host cells use to defend against viral infection. Some cellular proteins can function as restriction factors to limit viral infection by ubiquitin-dependent degradation. In this research, we identificated of CUL4B-DDB1-PRPF19 E3 Ubiquitin Ligase Complex can mediate proteasomal degradation of ORF6, leading to inhibition of viral replication. Moreover, the CUL4B activator etoposide alleviates disease development in a mouse infection model, suggesting that this agent or its derivatives may be used to treat infections caused by SARS-CoV-2. We believe that these results will be extremely useful for the scientific and clinic communities in their search for cues and preventive measures to combat the COVID-19 pandemic.</jats:p>
  • Access State: Open Access