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.

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.