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Schian, L.

Publications and source records attributed to Schian, L..

2 recordsLinked to original sources

CENTRA: Knowledge-Based Gene Contexuality Graphs Reveal Functional Master Regulators by Centrality and Fractality

Deciphering gene function via context-aware approaches is limited by various means. Especially static gene sets used in enrichment analyses and the lack of single-gene resolution in such analyses restrains the flexible association of genes with specific context. Here, we introduce CENTRA (Centrality-based Exploration of Network Topologies from Regulatory Assemblies), a framework that models gene contextuality through topic-specific gene co-occurrence networks derived from curated gene sets and associated literature. Using Latent Dirichlet Allocation on 12,045 abstracts linked to MSigDB C2 gene sets, we uncovered 27 biological topics and constructed corresponding topic-specific networks that reflect distinct biological states, perturbation conditions, and disease-related regulatory programs. Graph-topological metrics, including centrality, local fractality, and perturbation sensitivity, were computed for each gene to capture structural relevance within these topic-specific contexts. We demonstrate that topological profiles distinguish well-characterized regulators, identify emerging functional candidates, and reveal context-specific roles. Thereby, our framework enables the prioritization of understudied genes by assessing the robustness of their topological signatures across topic-specific networks. To support exploration of these results, we developed a publicly accessible interactive browser application, CENTRA, which enables dynamic navigation of networks and their functional annotations. CENTRA provides an interpretable, scalable framework for investigating context-dependent gene function and hypothesis generation, offering a novel entry point beyond traditional enrichment approaches. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=81 SRC="FIGDIR/small/662180v1_ufig1.gif" ALT="Figure 1"> View larger version (24K): org.highwire.dtl.DTLVardef@10e4eeorg.highwire.dtl.DTLVardef@125d5b4org.highwire.dtl.DTLVardef@f137aeorg.highwire.dtl.DTLVardef@7ea4e5_HPS_FORMAT_FIGEXP M_FIG C_FIG

bioinformatics↗

RAVER1 interconnects lethal EMT and miR/RISC activity by the control of alternative splicing

The RAVER1 protein was proposed to serve as a co-factor in guiding the PTBP-dependent control of alternative splicing (AS). Whether RAVER1 solely acts in concert with PTBPs and how it affects cancer cell fate remained elusive. Here we provide the first comprehensive investigation of RAVER1-controlled AS in cancer cell models and reveal a pro-oncogenic role of RAVER1 in tumor growth. This unravels that RAVER1 guides AS in synergy with PTBPs but more prominently serves PTBP1-independent roles in splicing. In cancer cells, one major function of RAVER1 is the control of proliferation and apoptosis, which involves the modulation of AS events within the miR/RISC pathway. Associated with this regulatory role, RAVER1 antagonizes lethal, TGFB-driven epithelial-mesenchymal-transition (EMT) by limiting TGFB signaling. RAVER1-modulated splicing events affect the insertion of protein interaction modules in factors guiding miR/RISC-dependent gene silencing. Most prominently, in all three human TNRC6 proteins, RAVER1 controls AS of GW-enriched motifs, which are essential for AGO2-binding. Disturbance of RAVER1-guided AS events in TNRC6 proteins and other facilitators of miR/RISC activity compromise miR/RISC activity which is essential to restrict TGFB signaling and lethal EMT.

molecular biology↗