TY - JOUR
T1 - GEMCAT - a new algorithm for gene expression-based prediction of metabolic alterations
AU - Sharma, Suraj
AU - Sauter, Roland
AU - Hotze, Madlen
AU - Prowatke, Aaron Marcellus Paul
AU - Niere, Marc
AU - Kipura, Tobias
AU - Egger, Anna Sophia
AU - Thedieck, Kathrin
AU - Kwiatkowski, Marcel
AU - Ziegler, Mathias
AU - Heiland, Ines
N1 - Publisher Copyright:
© 2025 The Author(s).
PY - 2025/3/1
Y1 - 2025/3/1
N2 - The interpretation of multi-omics datasets obtained from high-throughput approaches is important to understand disease-related physiological changes and to predict biomarkers in body fluids. We present a new metabolite-centred genome-scale metabolic modelling algorithm, the Gene Expression-based Metabolite Centrality Analysis Tool (GEMCAT). GEMCAT enables integration of transcriptomics or proteomics data to predict changes in metabolite concentrations, which can be verified by targeted metabolomics. In addition, GEMCAT allows to trace measured and predicted metabolic changes back to the underlying alterations in gene expression or proteomics and thus enables functional interpretation and integration of multi-omics data. We demonstrate the predictive capacity of GEMCAT on three datasets and genome-scale metabolic networks from two different organisms: (i) we integrated transcriptomics and metabolomics data from an engineered human cell line with a functional deletion of the mitochondrial NAD transporter; (ii) we used a large multi-tissue multi-omics dataset from rats for transcriptome- and proteome-based prediction and verification of training-induced metabolic changes and achieved an average prediction accuracy of 70%; and (iii) we used proteomics measurements from patients with inflammatory bowel disease and verified the predicted changes using metabolomics data from the same patients. For this dataset, the prediction accuracy achieved by GEMCAT was 79%.
AB - The interpretation of multi-omics datasets obtained from high-throughput approaches is important to understand disease-related physiological changes and to predict biomarkers in body fluids. We present a new metabolite-centred genome-scale metabolic modelling algorithm, the Gene Expression-based Metabolite Centrality Analysis Tool (GEMCAT). GEMCAT enables integration of transcriptomics or proteomics data to predict changes in metabolite concentrations, which can be verified by targeted metabolomics. In addition, GEMCAT allows to trace measured and predicted metabolic changes back to the underlying alterations in gene expression or proteomics and thus enables functional interpretation and integration of multi-omics data. We demonstrate the predictive capacity of GEMCAT on three datasets and genome-scale metabolic networks from two different organisms: (i) we integrated transcriptomics and metabolomics data from an engineered human cell line with a functional deletion of the mitochondrial NAD transporter; (ii) we used a large multi-tissue multi-omics dataset from rats for transcriptome- and proteome-based prediction and verification of training-induced metabolic changes and achieved an average prediction accuracy of 70%; and (iii) we used proteomics measurements from patients with inflammatory bowel disease and verified the predicted changes using metabolomics data from the same patients. For this dataset, the prediction accuracy achieved by GEMCAT was 79%.
UR - http://www.scopus.com/inward/record.url?scp=85216960678&partnerID=8YFLogxK
U2 - 10.1093/nargab/lqaf003
DO - 10.1093/nargab/lqaf003
M3 - Article
AN - SCOPUS:85216960678
SN - 2631-9268
VL - 7
JO - NAR genomics and bioinformatics
JF - NAR genomics and bioinformatics
IS - 1
M1 - lqaf003
ER -