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Effect of LINC01315 depletion and overexpression on proliferation of OMM2.3 uveal melanoma cells

GSE272013 Homo sapiens Expression profiling by high throughput sequencing 6 samples Submitted 2024/07/16 Platform GPL16791
Summary
Cell proliferation disorders contribute to several diseases including cardiac developmental defects and tumours,and identifying pivotal factors that modulate the cell proliferation process is important. In this study, we identified a short peptide, YAPer-ORF, encoded by the long-stranded non-coding RNA gene LINC01315. we clarified the biological function of YAPer-ORF in promoting cell proliferation using gene manipulation and examined various cell lines including OMM2.3. In terms of the molecular mechanism, we found that YAPer-ORF regulates YAP intranuclear kinase PRP4K, while coercing GNAQ/11 mutants to undergo nuclear translocation and inhibit transcription of critical factors in the Hippo signalling pathway to synergistically activate YAP activity.We finally validated our findings in transgenic mice with cardiac-specific expression and nude mouse models of tumour formation. Together, the present study elucidates a novel regulatory mechanism of the Hippo signalling pathway and provides a new intervention target for disorders arising from dysregulation of the Hippo signalling pathway.
Published in
The LINC01315-encoded small protein YAPer-ORF competes with PRP4k to hijack YAP signaling to aberrantly promote cell growth
Xie Z, Li C, Huang R et al. · Cell death and differentiation 2025 · PMID 39962243 · doi:10.1038/s41418-025-01449-z
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Direct links to NCBI, no account and no request form: the whole study as GSE272013_RAW.tar, processed values as the series matrix, the supplementary file directory, and per-sample supplementary files for any of the 6 samples. Raw sequencing reads are also available from ENA.

Also filed as BioProject PRJNA1134629 and SRA study SRP519296. Searching any of these in the dataset finder brings you back here.

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