SnoBIRD: a tool to identify C/D box snoRNAs and refine their annotation across all eukaryotes

Small nucleolar RNAs (snoRNAs), a group of noncoding RNAs present amongst all eukaryotes, are most extensively characterized for their regulation of ribosome biogenesis and splicing. Despite their central roles, current snoRNA annotations remain incomplete. Several eukaryote genome annotations contain few or no snoRNAs, and none distinguish expressed snoRNAs from their pseudogenes-a recently characterized snoRNA subclass with distinct features and expression levels. To address this, we developed SnoBIRD, a BERT-based C/D box snoRNA predictor trained on snoRNAs spanning all eukaryote kingdoms. We show that SnoBIRD outperforms existing tools and is the only predictor capable of identifying snoRNA pseudogenes using biologically relevant signal. Applied on the fission yeast and human genomes, we demonstrate that only SnoBIRD scales well with genome size in terms of runtime, and we identify and experimentally validate several new SnoBIRD-predicted C/D box snoRNAs. By running SnoBIRD on multiple eukaryote genomes, we identify hundreds of novel snoRNA candidates and highlight SnoBIRD's usefulness to determine the evolutionary paths of snoRNAs distributed across different species. Overall, SnoBIRD represents a user-friendly and efficient tool for reliably predicting C/D box snoRNAs and their pseudogenes across any eukaryote genome.

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Publication Details

Journal
Nucleic Acids Research
Published
2025-07-14
DOI
https://doi.org/10.1093/nar/gkaf708
Citations
1
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
0.81

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article

SnoBIRD: a tool to identify C/D box snoRNAs and refine their annotation across all eukaryotes

Sébastien Durand, Pierre‐Étienne Jacques, Étienne Fafard-Couture, Mark A. Bayfield et al.
1 citations
Nucleic Acids Research
RNA modifications and cancer
0.81
article

SnoBIRD: a tool to identify C/D box snoRNAs and refine their annotation across all eukaryotes

Sébastien Durand, Pierre‐Étienne Jacques, Étienne Fafard-Couture, Mark A. Bayfield, Laurence Faucher‐Giguère, François Bachand, Virginie Marcel, Sherif Abou Elela, Michelle S. Scott, Mélodie Berthoumieux, Jordan Hedjam, Cédric Boulanger, Vanessa Sinagoga
article en
1 citations

Abstract

Small nucleolar RNAs (snoRNAs), a group of noncoding RNAs present amongst all eukaryotes, are most extensively characterized for their regulation of ribosome biogenesis and splicing. Despite their central roles, current snoRNA annotations remain incomplete. Several eukaryote genome annotations contain few or no snoRNAs, and none distinguish expressed snoRNAs from their pseudogenes-a recently characterized snoRNA subclass with distinct features and expression levels. To address this, we developed SnoBIRD, a BERT-based C/D box snoRNA predictor trained on snoRNAs spanning all eukaryote kingdoms. We show that SnoBIRD outperforms existing tools and is the only predictor capable of identifying snoRNA pseudogenes using biologically relevant signal. Applied on the fission yeast and human genomes, we demonstrate that only SnoBIRD scales well with genome size in terms of runtime, and we identify and experimentally validate several new SnoBIRD-predicted C/D box snoRNAs. By running SnoBIRD on multiple eukaryote genomes, we identify hundreds of novel snoRNA candidates and highlight SnoBIRD's usefulness to determine the evolutionary paths of snoRNAs distributed across different species. Overall, SnoBIRD represents a user-friendly and efficient tool for reliably predicting C/D box snoRNAs and their pseudogenes across any eukaryote genome.

Nucleic Acids ResearchVol. 53(14)
Université Claude Bernard Lyon 1 (FR), Centre National de la Recherche Scientifique (FR), Université de Sherbrooke (CA), Inserm (FR), York University (CA), Centre Hospitalier Universitaire de Sherbrooke (CA), Centre de Recherche en Cancérologie de Lyon (FR)
Natural Sciences and Engineering Research Council of Canada, Fonds de Recherche du Québec - Santé
Life in Land
Openalex Percentile: Top 25%
RNA modifications and cancer
0.81
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