ArticleBioinformatics (Oxford, England)2016
Predicting G protein-coupled receptor downstream signaling by tissue expression.
Article in Bioinformatics (Oxford, England), 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 17 citations in OpenAlex.
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- A deep proteome and transcriptome abundance atlas of 29 healthy human tissues.Molecular systems biology · 2019Article
- Informatics and Computational Methods in Natural Product Drug Discovery: A Review and Perspectives.Frontiers in genetics · 2019Review
- Tissue-Specific Analysis of Pharmacological Pathways.CPT: pharmacometrics & systems pharmacology · 2018Article
- Conformational Profiling of the AT1 Angiotensin II Receptor Reflects Biased Agonism, G Protein Coupling, and Cellular Context.The Journal of biological chemistry · 2017Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors at 1 institution in 1 country.
Funding
Abstract
motivationG protein-coupled receptors (GPCRs) are central to how cells respond to their environment and a major class of pharmacological targets. However, comprehensive knowledge of which pathways are activated and deactivated by these essential sensors is largely unknown. To better understand the mechanism of GPCR signaling system, we integrated five independent genome-wide expression datasets, representing 275 human tissues and cell lines, with protein-protein interactions and functional pathway data.
resultsWe found that tissue-specificity plays a crucial part in the function of GPCR signaling system. Only a few GPCRs are expressed in each tissue, which are coupled by different combinations of G-proteins or β-arrestins to trigger specific downstream pathways. Based on this finding, we predicted the downstream pathways of GPCR in human tissues and validated our results with L1000 knockdown data. In total, we identified 154,988 connections between 294 GPCRs and 690 pathways in 240 tissues and cell types. AVAILABILITY AND IMPLEMENTATION: The source code and results supporting the conclusions of this article are available at http://tatonettilab.org/resources/GOTE/source_code/ CONTACT: nick.tatonetti@columbia.eduSupplementary information: Supplementary data are available at Bioinformatics online.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.