mGem: Noncanonical nucleic acid structures—powerful but neglected antiviral targets

This perspective highlights the emerging significance of noncanonical nucleic acid structures-such as G-quadruplexes, Z-DNA/Z-RNA, and cruciforms-in viral genomes. Once considered structural oddities, these motifs are now recognized as critical regulators of viral replication, transcription, genome stability, and host-pathogen interactions. Despite mounting evidence of their functional relevance and therapeutic potential, these structures remain largely overlooked in virology and antiviral drug development. Their unique conformations offer highly specific molecular targets, with several small molecules already demonstrating the ability to modulate viral gene expression by stabilizing or destabilizing these motifs. The persistent underestimation of non-B DNA/RNA structures represents a missed opportunity in the fight against viral diseases. By synthesizing recent discoveries and emphasizing their biological and pharmacological promise, we aim to elevate awareness and catalyze interdisciplinary research. Harnessing the structural diversity of viral genomes could unlock novel antiviral strategies with high specificity and minimal off-target effects.

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Publication Details

Journal
mBio
Published
2025-09-29
DOI
https://doi.org/10.1128/mbio.02730-25
Citations
1
Primary Topic
RNA and protein synthesis mechanisms
Type
article
Field-Weighted Citation Impact
0.81
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article

mGem: Noncanonical nucleic acid structures—powerful but neglected antiviral targets

Martin Bartas, Petr Pečínka, Václav Brázda, Richard P. Bowater
1 citations
mBio
RNA and protein synthesis mechanisms
0.81
article

mGem: Noncanonical nucleic acid structures—powerful but neglected antiviral targets

Martin Bartas, Petr Pečínka, Václav Brázda, Richard P. Bowater
article en
1 citations

Abstract

This perspective highlights the emerging significance of noncanonical nucleic acid structures-such as G-quadruplexes, Z-DNA/Z-RNA, and cruciforms-in viral genomes. Once considered structural oddities, these motifs are now recognized as critical regulators of viral replication, transcription, genome stability, and host-pathogen interactions. Despite mounting evidence of their functional relevance and therapeutic potential, these structures remain largely overlooked in virology and antiviral drug development. Their unique conformations offer highly specific molecular targets, with several small molecules already demonstrating the ability to modulate viral gene expression by stabilizing or destabilizing these motifs. The persistent underestimation of non-B DNA/RNA structures represents a missed opportunity in the fight against viral diseases. By synthesizing recent discoveries and emphasizing their biological and pharmacological promise, we aim to elevate awareness and catalyze interdisciplinary research. Harnessing the structural diversity of viral genomes could unlock novel antiviral strategies with high specificity and minimal off-target effects.

mBioVol. 16(11)
University of East Anglia (GB), University of Ostrava (CZ), Czech Academy of Sciences, Institute of Biophysics (CZ)
Openalex Percentile: Top 23%
RNA and protein synthesis mechanisms
0.81
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