Frontiers in Cellular and Infection Microbiology (Aug 2021)

SARS-CoV-2 Membrane Glycoprotein M Triggers Apoptosis With the Assistance of Nucleocapsid Protein N in Cells

  • Yujie Ren,
  • Yujie Ren,
  • An Wang,
  • An Wang,
  • An Wang,
  • Yuan Fang,
  • Ting Shu,
  • Ting Shu,
  • Di Wu,
  • Di Wu,
  • Chong Wang,
  • Chong Wang,
  • Muhan Huang,
  • Muhan Huang,
  • Juan Min,
  • Liang Jin,
  • Wei Zhou,
  • Yang Qiu,
  • Yang Qiu,
  • Yang Qiu,
  • Xi Zhou,
  • Xi Zhou,
  • Xi Zhou,
  • Xi Zhou

DOI
https://doi.org/10.3389/fcimb.2021.706252
Journal volume & issue
Vol. 11

Abstract

Read online

The pandemic of COVID-19 by SARS-CoV-2 has become a global disaster. However, we still don’t know how specific SARS-CoV-2-encoded proteins contribute to viral pathogenicity. We found that SARS-CoV-2-encoded membrane glycoprotein M could induce caspase-dependent apoptosis via interacting with PDK1 and inhibiting the activation of PDK1-PKB/Akt signaling. Our investigation further revealed that SARS-CoV-2-encoded nucleocapsid protein N could specifically enhance the M-induced apoptosis via interacting with both M and PDK1, therefore strengthening M-mediated attenuation of PDK1-PKB/Akt interaction. Furthermore, when the M-N interaction was disrupted via certain rationally designed peptides, the PDK1-PKB/Akt signaling was restored, and the boosting activity of N on the M-triggered apoptosis was abolished. Overall, our findings uncovered a novel mechanism by which SARS-CoV-2-encoded M triggers apoptosis with the assistance of N, which expands our understanding of the two key proteins of SARS-CoV-2 and sheds light on the pathogenicity of this life-threatening virus.

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