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Published on: May 12, 2023
CNBP Binds and Unfolds In Vitro G-Quadruplexes Formed in the SARS-CoV-2 Positive and Negative Genome Strands
Georgina Bezzi1, Ernesto J Piga1, Andrés Binolfi1,2
1Instituto de Biología Molecular y Celular de Rosario (IBR), Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET), Universidad Nacional de Rosario (UNR), Ocampo y Esmeralda, Rosario S200EZP, Santa Fe, Argentina.
Abstract:
The Coronavirus Disease 2019 (COVID-19) pandemic has become a global health emergency with no effective medical treatment and with incipient vaccines. It is caused by a new positive-sense RNA virus called severe acute respiratory syndrome-related coronavirus 2 (SARS-CoV-2). G-quadruplexes (G4s) are nucleic acid secondary structures involved in the control of a variety of biological processes including viral replication. Using several G4 prediction tools, we identified highly putative G4 sequences (PQSs) within the positive-sense (+gRNA) and negative-sense (-gRNA) RNA strands of SARS-CoV-2 conserved in related betacoronaviruses. By using multiple biophysical techniques, we confirmed the formation of two G4s in the +gRNA and provide the first evidence of G4 formation by two PQSs in the -gRNA of SARS-CoV-2. Finally, biophysical and molecular approaches were used to demonstrate for the first time that CNBP, the main human cellular protein bound to SARS-CoV-2 RNA genome, binds and promotes the unfolding of G4s formed by both strands of SARS-CoV-2 RNA genome. Our results suggest that G4s found in SARS-CoV-2 RNA genome and its negative-sense replicative intermediates, as well as the cellular proteins that interact with them, are relevant factors for viral genes expression and replication cycle, and may constitute interesting targets for antiviral drugs development.
Insights
G-quadruplexes (G4s) in SARS-CoV-2 RNA are confirmed, influencing viral replication. Human protein CNBP binds and unfolds these G4 structures, suggesting new antiviral targets.
Area of Science:
- Virology
- Molecular Biology
- Structural Biology
Background:
- Coronavirus Disease 2019 (COVID-19) is a global health emergency caused by SARS-CoV-2.
- G-quadruplexes (G4s) are nucleic acid structures regulating biological processes, including viral replication.
Purpose of the Study:
- To identify and characterize G-quadruplexes (G4s) in the SARS-CoV-2 genome.
- To investigate the interaction between SARS-CoV-2 G4s and human cellular proteins.
Main Methods:
- Bioinformatic G4 prediction tools.
- Multiple biophysical techniques (e.g., spectroscopy, FRET).
- Molecular approaches to study protein-RNA interactions.
Main Results:
- Identified putative G4 sequences in both positive-sense and negative-sense RNA strands of SARS-CoV-2.
- Confirmed G4 formation in two regions of the positive-sense RNA and two regions of the negative-sense RNA.
- Demonstrated that human protein CNBP binds to and unfolds SARS-CoV-2 RNA G4s.
Conclusions:
- G4 structures in SARS-CoV-2 RNA and their interactions with cellular proteins are crucial for viral gene expression and replication.
- These G4s and interacting proteins represent potential targets for novel antiviral drug development.
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