tetano
Editor, Senior Moderator
J Med Virol
. 2024 Jan;96(1):e29396.
doi: 10.1002/jmv.29396. SARS-CoV-2 NSP12 utilizes various host splicing factors for replication and splicing regulation
Li Yang[SUP] 1 [/SUP], Xiao-Tao Zeng[SUP] 1 [/SUP], Rong-Hua Luo[SUP] 2 [/SUP], Si-Xue Ren[SUP] 1 [/SUP], Lin-Lin Liang[SUP] 1 [/SUP], Qiu-Xia Huang[SUP] 1 [/SUP], Ying Tang[SUP] 1 [/SUP], Hong Fan[SUP] 1 [/SUP], Hai-Yan Ren[SUP] 1 [/SUP], Wan-Jiang Zhang[SUP] 3 [/SUP], Yong-Tang Zheng[SUP] 2 [/SUP], Wei Cheng[SUP] 1 [/SUP]
Affiliations
The RNA-dependent RNA polymerase (RdRp) is a crucial element in the replication and transcription of RNA viruses. Although the RdRps of lethal human coronaviruses severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), SARS-CoV, and Middle East respiratory syndrome coronavirus (MERS-CoV) have been extensively studied, the molecular mechanism of the catalytic subunit NSP12, which is involved in pathogenesis, remains unclear. In this study, the biochemical and cell biological results demonstrate the interactions between SARS-CoV-2 NSP12 and seven host proteins, including three splicing factors (SLU7, PPIL3, and AKAP8). The entry efficacy of SARS-CoV-2 considerably decreased when SLU7 or PPIL3 was knocked out, indicating that abnormal splicing of the host genome was responsible for this occurrence. Furthermore, the polymerase activity and stability of SARS-CoV-2 RdRp were affected by the three splicing factors to varying degrees. In addition, NSP12 and its homologues from SARS-CoV and MERS-CoV suppressed the alternative splicing of cellular genes, which were influenced by the three splicing factors. Overall, our research illustrates that SARS-CoV-2 NSP12 can engage with various splicing factors, thereby impacting virus entry, replication, and gene splicing. This not only improves our understanding of how viruses cause diseases but also lays the foundation for the development of antiviral therapies.
Keywords: RNA-dependent RNA polymerase; human coronaviruses; splicing regulation; virus replication; virus-host interaction.
. 2024 Jan;96(1):e29396.
doi: 10.1002/jmv.29396. SARS-CoV-2 NSP12 utilizes various host splicing factors for replication and splicing regulation
Li Yang[SUP] 1 [/SUP], Xiao-Tao Zeng[SUP] 1 [/SUP], Rong-Hua Luo[SUP] 2 [/SUP], Si-Xue Ren[SUP] 1 [/SUP], Lin-Lin Liang[SUP] 1 [/SUP], Qiu-Xia Huang[SUP] 1 [/SUP], Ying Tang[SUP] 1 [/SUP], Hong Fan[SUP] 1 [/SUP], Hai-Yan Ren[SUP] 1 [/SUP], Wan-Jiang Zhang[SUP] 3 [/SUP], Yong-Tang Zheng[SUP] 2 [/SUP], Wei Cheng[SUP] 1 [/SUP]
Affiliations
- PMID: 38235848
- DOI: 10.1002/jmv.29396
The RNA-dependent RNA polymerase (RdRp) is a crucial element in the replication and transcription of RNA viruses. Although the RdRps of lethal human coronaviruses severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), SARS-CoV, and Middle East respiratory syndrome coronavirus (MERS-CoV) have been extensively studied, the molecular mechanism of the catalytic subunit NSP12, which is involved in pathogenesis, remains unclear. In this study, the biochemical and cell biological results demonstrate the interactions between SARS-CoV-2 NSP12 and seven host proteins, including three splicing factors (SLU7, PPIL3, and AKAP8). The entry efficacy of SARS-CoV-2 considerably decreased when SLU7 or PPIL3 was knocked out, indicating that abnormal splicing of the host genome was responsible for this occurrence. Furthermore, the polymerase activity and stability of SARS-CoV-2 RdRp were affected by the three splicing factors to varying degrees. In addition, NSP12 and its homologues from SARS-CoV and MERS-CoV suppressed the alternative splicing of cellular genes, which were influenced by the three splicing factors. Overall, our research illustrates that SARS-CoV-2 NSP12 can engage with various splicing factors, thereby impacting virus entry, replication, and gene splicing. This not only improves our understanding of how viruses cause diseases but also lays the foundation for the development of antiviral therapies.
Keywords: RNA-dependent RNA polymerase; human coronaviruses; splicing regulation; virus replication; virus-host interaction.