Illuminating Dark Proteins using Reactome Pathways
Brunson, T.; Sanati, N.; Matthews, L.; Haw, R.; Beavers, D.; Shorser, S.; Sevilla, C.; Viteri, G.; Conley, P.; Rothfels, K.; Hermjakob, H.; Stein, L.; D'Eustachio, P.; Wu, G.
Show abstract
Limited knowledge about a substantial portion of protein coding genes, known as "dark" proteins, hinders our understanding of their functions and potential therapeutic applications. To address this, we leveraged Reactome, the most comprehensive, open source, open-access pathway knowledgebase, to contextualize dark proteins within biological pathways. By integrating multiple resources and employing a random forest classifier trained on 106 protein/gene pairwise features, we predicted functional interactions between dark proteins and Reactome-annotated proteins. We then developed three scores to measure the interactions between dark proteins and Reactome pathways, utilizing enrichment analysis and fuzzy logic simulations. Correlation analysis of these scores with an independent single-cell RNA sequencing dataset provided supporting evidence for this approach. Furthermore, systematic natural language processing (NLP) analysis of over 22 million PubMed abstracts and manual checking of the literature associated with 20 randomly selected dark proteins reinforced the predicted interactions between proteins and pathways. To enhance the visualization and exploration of dark proteins within Reactome pathways, we developed the Reactome IDG portal, deployed at https://idg.reactome.org, a web application featuring tissue-specific protein and gene expression overlay, as well as drug interactions. Our integrated computational approach, together with the user-friendly web platform, offers a valuable resource for uncovering potential biological functions and therapeutic implications of dark proteins.
Matching journals
The top 6 journals account for 50% of the predicted probability mass.
Similar papers in this journal
- HELP: A computational framework for labelling and predicting human common and context-specific essential genes 95%
- Network models of protein phosphorylation, acetylation, and ubiquitination connect metabolic and cell signaling pathways in lung cancer 95%
- Multi-omics subtyping of hepatocellular carcinoma patients using a Bayesian network mixture model 95%
Similar papers in this journal
- Predicting Gene Disease Associations With Knowledge Graph Embeddings For Diseases With Curtailed Information 94%
- Decoding proteome functional information in model organisms using protein language models. 94%
- Comprehensive benchmark of differential transcript usage analysis for static and dynamic conditions 94%
Similar papers in this journal
- SUBATOMIC: a SUbgraph BAsed mulTi-OMIcs Clustering framework to analyze integrated multi-edge networks 96%
- scTensor detects many-to-many cell-cell interactions from single cell RNA-sequencing data 95%
- DeltaNeTS+: Elucidating the mechanism of drugs and diseases using gene expression and transcriptional regulatory networks 95%
Similar papers in this journal
"Similar papers" are the closest papers from that journal in the model's embedding space. They show what the match is built on, but the ranking comes mostly from a classifier over the whole training set, not from these examples alone.