Show Notes
Zhou S et al., Nat Commun - This episode examines how the cancer-associated Pol III transcript snaR-A binds core splicing factors, localizes near nuclear speckles, perturbs U2-dependent splicing to increase intron retention, and promotes cell proliferation linked to poorer patient outcomes. Key terms: snaR-A, splicing, SF3B2, intron retention, nuclear speckles.
Study Highlights:
Proteomic pull-downs and CLIP analyses reveal snaR-A interactions with RNA chaperones (La, ILF3) and multiple splicing factors, with PAR-CLIP and CLIP-qPCR supporting a direct interaction with the U2 snRNP subunit SF3B2. HCR-RNA-FISH and SON TSA-seq place snaR-A in subnuclear foci adjacent to nuclear speckles and show snaR-A gene clusters are speckle-proximal. Functional genomics show snaR-A overexpression increases intron retention while snaR-A depletion reduces intron retention and enhances splicing of transcripts marked by high U2 occupancy and speckle proximity, and snaR-A overexpression selectively reduces SF3B2 protein levels. Phenotypically, snaR-A depletion lowers proliferation in HEK293T cells, snaR-A gene activity correlates with proliferation markers across primary tumors and predicts worse survival, and rescued splicing increases protein abundance for tumor-suppressive targets such as OGFR.
Conclusion:
snaR-A acts as a nuclear antagonist of U2-dependent splicing near speckles, promoting cell proliferation and providing a non-mutational route to splicing dysregulation in cancer
Music:
Enjoy the music based on this article at the end of the episode.
First author:
Zhou S
Journal:
Nature Communications
DOI:
10.1038/s41467-025-65448-x
Reference:
Zhou S, Lizarazo S, Chorghade S, Mouli L, Cheng R, KC R, Kalsotra A, Van Bortle K. Cancer-associated snaR-A noncoding RNA interacts with core splicing machinery and disrupts processing of mRNA subpopulations. Nat Commun. 2025;16:10460. https://doi.org/10.1038/s41467-025-65448-x
License:
This episode is based on an open-access article published under the Creative Commons Attribution 4.0 International License (CC BY 4.0) – https://creativecommons.org/licenses/by/4.0/
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Episode link: https://basebybase.com/episodes/snar-a-splicing-disruption
️ Episode:
222: snaR-A hijacks splicing to drive proliferation
️ Season:
1
Article title:
Cancer-associated snaR-A noncoding RNA interacts with core splicing machinery and disrupts processing of mRNA subpopulations
QC:
This episode was checked against the original article PDF and publication metadata for the episode release published on 2025-12-08.
QC Scope:
- article metadata and core scientific claims from the narration
- excludes analogies, intro/outro, and music
- transcript coverage: Audited the transcript's core mechanistic and phenotypic claims described in the Nature Communications article: snaR-A interactions with SF3B2 and splicing machinery, subnuclear speckle localization, intron retention changes with overexpression/depletion, effects on proliferation and OGFR, and clinical correlations.
- transcript topics: Pol III overactivity and snaR-A origin in cancer; snaR-A interactions with splicing factors (SF3B2, U2 snRNP); subnuclear localization near nuclear speckles; intron retention and splicing efficiency changes; effects of snaR-A depletion/overexpression on proliferation and OGFR; clinical associations: snaR-A activity and patient survival
QC Summary:
- factual score: 10/10
- metadata score: 10/10
- supported core claims: 8
- claims flagged for review: 0
- metadata checks passed: 4
- metadata issues found: 0
Metadata Audited:
- article_doi
- article_title
- article_journal
- license
Factual Items Audited:
- snaR-A interacts with core mRNA splicing machinery including SF3B2
- snaR-A localizes near nuclear speckles and associates with splicing factors
- overexpression of snaR-A increases intron retention, especially for U2-bound, speckle-proximal transcripts
- depletion of snaR-A reduces intron retention and improves splicing of U2-resident, speckle-proximal transcripts
- splicing improvements after snaR-A depletion correlate with increased OGFR protein levels (tumor suppressor)
- snaR-A depletion reduces cell proliferation in HEK293T cells
QC result: Pass.
