| Literature DB >> 35497496 |
Hamid Hamzeiy1, Daniela Ferretti1, Maria S Robles2, Jürgen Cox1,3.
Abstract
We introduce Metis, a new plugin for the Perseus software aimed at analyzing quantitative multi-omics data based on metabolic pathways. Data from different omics types are connected through reactions of a genome-scale metabolic-pathway reconstruction. Metabolite concentrations connect through the reactants, while transcript, protein, and protein post-translational modification (PTM) data are associated through the enzymes catalyzing the reactions. Supported experimental designs include static comparative studies and time-series data. As an example for the latter, we combine circadian mouse liver multi-omics data and study the contribution of cycles of phosphoproteome and metabolome to enzyme activity regulation. Our analysis resulted in 52 pairs of cycling phosphosites and metabolites connected through a reaction. The time lags between phosphorylation and metabolite peak show non-uniform behavior, indicating a major contribution of phosphorylation in the modulation of enzymatic activity.Entities:
Keywords: Metis; Perseus; circadian rhythms; enzyme activity regulation; metabolic networks; metabolomics; multi-omics; phosphoproteomics; proteomics; transcriptomics
Year: 2022 PMID: 35497496 PMCID: PMC9046241 DOI: 10.1016/j.crmeth.2022.100198
Source DB: PubMed Journal: Cell Rep Methods ISSN: 2667-2375