Abstract
We describe a function-driven approach to the analysis of metabolism which takes into account the phylogenetic origin of biochemical reactions to reveal subtle lineage-specific metabolic innovations, undetectable by more traditional methods based on sequence comparison. The origins of reactions and thus entire pathways are inferred using a simple taxonomic classification scheme that describes the evolutionary course of events towards the lineage of interest. We investigate the evolutionary history of the human metabolic network extracted from a metabolic database, construct a network of interconnected pathways and classify this network according to the taxonomic categories representing eukaryotes, metazoa and vertebrates. It is demonstrated that lineage-specific innovations correspond to reactions and pathways associated with key phenotypic changes during evolution, such as the emergence of cellular organelles in eukaryotes, cell adhesion cascades in metazoa and the biosynthesis of complex cell-specific biomolecules in vertebrates. This phylogenetic view of metabolic networks puts gene innovations within an evolutionary context, demonstrating how the emergence of a phenotype in a lineage provides a platform for the development of specialized traits.
MeSH Terms
Cholesterol/metabolism
Computational Biology/methods
Databases, Genetic
Evolution, Molecular
Glycosphingolipids/metabolism
Glycosylation
Humans
Metabolic Networks and Pathways
Models, Genetic
Phylogeny
Chemicals
Glycosphingolipids
Cholesterol
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Freilich Shiri
The European Bioinformatics Institute, EMBL Cambridge Outstation, Wellcome Trust Genome Campus, Cambridge CB10 1SD, UK.
[email protected]
Goldovsky Leon
Ouzounis Christos A
Thornton Janet M
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