tetano
Editor, Senior Moderator
J Cell Biol
. 2023 Oct 2;222(10):e202303002.
doi: 10.1083/jcb.202303002. Epub 2023 Sep 8. The Orf9b protein of SARS-CoV-2 modulates mitochondrial protein biogenesis
Svenja Lenhard[SUP] #[/SUP][SUP] 1 [/SUP], Sarah Gerlich[SUP] #[/SUP][SUP] 2 3 [/SUP], Azkia Khan[SUP] 1 [/SUP], Saskia Rödl[SUP] 1 [/SUP], Jan-Eric Bökenkamp[SUP] 4 [/SUP], Esra Peker[SUP] 2 3 [/SUP], Christine Zarges[SUP] 2 3 [/SUP], Janina Faust[SUP] 1 [/SUP], Zuzana Storchova[SUP] 4 [/SUP], Markus Räschle[SUP] 4 [/SUP], Jan Riemer[SUP] 2 3 [/SUP], Johannes M Herrmann[SUP] 1 [/SUP]
Affiliations
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) expresses high amounts of the protein Orf9b to target the mitochondrial outer membrane protein Tom70. Tom70 serves as an import receptor for mitochondrial precursors and, independently of this function, is critical for the cellular antiviral response. Previous studies suggested that Orf9b interferes with Tom70-mediated antiviral signaling, but its implication for mitochondrial biogenesis is unknown. In this study, we expressed Orf9b in human HEK293 cells and observed an Orf9b-mediated depletion of mitochondrial proteins, particularly in respiring cells. To exclude that the observed depletion was caused by the antiviral response, we generated a yeast system in which the function of human Tom70 could be recapitulated. Upon expression of Orf9b in these cells, we again observed a specific decline of a subset of mitochondrial proteins and a general reduction of mitochondrial volume. Thus, the SARS-CoV-2 virus is able to modulate the mitochondrial proteome by a direct effect of Orf9b on mitochondrial Tom70-dependent protein import.
. 2023 Oct 2;222(10):e202303002.
doi: 10.1083/jcb.202303002. Epub 2023 Sep 8. The Orf9b protein of SARS-CoV-2 modulates mitochondrial protein biogenesis
Svenja Lenhard[SUP] #[/SUP][SUP] 1 [/SUP], Sarah Gerlich[SUP] #[/SUP][SUP] 2 3 [/SUP], Azkia Khan[SUP] 1 [/SUP], Saskia Rödl[SUP] 1 [/SUP], Jan-Eric Bökenkamp[SUP] 4 [/SUP], Esra Peker[SUP] 2 3 [/SUP], Christine Zarges[SUP] 2 3 [/SUP], Janina Faust[SUP] 1 [/SUP], Zuzana Storchova[SUP] 4 [/SUP], Markus Räschle[SUP] 4 [/SUP], Jan Riemer[SUP] 2 3 [/SUP], Johannes M Herrmann[SUP] 1 [/SUP]
Affiliations
- PMID: 37682539
- DOI: 10.1083/jcb.202303002
The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) expresses high amounts of the protein Orf9b to target the mitochondrial outer membrane protein Tom70. Tom70 serves as an import receptor for mitochondrial precursors and, independently of this function, is critical for the cellular antiviral response. Previous studies suggested that Orf9b interferes with Tom70-mediated antiviral signaling, but its implication for mitochondrial biogenesis is unknown. In this study, we expressed Orf9b in human HEK293 cells and observed an Orf9b-mediated depletion of mitochondrial proteins, particularly in respiring cells. To exclude that the observed depletion was caused by the antiviral response, we generated a yeast system in which the function of human Tom70 could be recapitulated. Upon expression of Orf9b in these cells, we again observed a specific decline of a subset of mitochondrial proteins and a general reduction of mitochondrial volume. Thus, the SARS-CoV-2 virus is able to modulate the mitochondrial proteome by a direct effect of Orf9b on mitochondrial Tom70-dependent protein import.