Accepted_test
Synthetic biology, a rapidly advancing field, involves constructing new organisms with specific traits through genome synthesis or deep reorganization using genetic engineering, bioengineering, systems biology and bioinformatics. Systems biology, integrating omics data and metabolic modeling, offers a promising strategy for enhancing biotechnological properties. Genome-scale metabolic models (GEMs) are invaluable for understanding organism metabolism, while context-specific models enable studying metabolism under specific conditions. Despite advancements, the molecular basis of growth differences among chicken breeds remains poorly understood. The main goal of the study is to explore metabolic differences between fast- and slow-growing chicken breeds using context-specific genome-scale models (csGEMs). Our pan-genomic GRCg6a assembly was used as a basis for transcriptomics profiling. We improved the model's quality, rendering it more conducive to biological interpretation, according to Memote test-suite. By integrating transcriptomic data into iES1300 model, we obtaining csGEMs, from which we identified key metabolic reactions and genes linked to growth. Context-specific models of fast-growing muscle tissues exhibited notable disparities from predictions for slow-growing tissues regarding growth rates predicted by the flux balance analysis. Our study elucidated the critical metabolic pathways and regulatory nodes influencing the varying growth rates observed in fast- and slow-growing chicken breeds.