ReCodLiver0.9: Overcoming Challenges in Genome-Scale Metabolic Reconstruction of a Non-model Species

The availability of genome sequences, annotations, and knowledge of the biochemistry underlying metabolic transformations has led to the generation of metabolic network reconstructions for a wide range of organisms in bacteria, archaea, and eukaryotes. When modeled using mathematical representations...

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Bibliographic Details
Published in:Frontiers in Molecular Biosciences
Main Authors: Hanna, Eileen Marie, Zhang, Xiaokang, Eide, Marta, Fallahi, Shirin, Furmanek, Tomasz, Yadetie, Fekadu, Zielinski, Daniel Craig, Goksøyr, Anders, Jonassen, Inge
Format: Text
Language:English
Published: Frontiers Media S.A. 2020
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Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7726423/
http://www.ncbi.nlm.nih.gov/pubmed/33324679
https://doi.org/10.3389/fmolb.2020.591406
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Summary:The availability of genome sequences, annotations, and knowledge of the biochemistry underlying metabolic transformations has led to the generation of metabolic network reconstructions for a wide range of organisms in bacteria, archaea, and eukaryotes. When modeled using mathematical representations, a reconstruction can simulate underlying genotype-phenotype relationships. Accordingly, genome-scale metabolic models (GEMs) can be used to predict the response of organisms to genetic and environmental variations. A bottom-up reconstruction procedure typically starts by generating a draft model from existing annotation data on a target organism. For model species, this part of the process can be straightforward, due to the abundant organism-specific biochemical data. However, the process becomes complicated for non-model less-annotated species. In this paper, we present a draft liver reconstruction, ReCodLiver0.9, of Atlantic cod (Gadus morhua), a non-model teleost fish, as a practicable guide for cases with comparably few resources. Although the reconstruction is considered a draft version, we show that it already has utility in elucidating metabolic response mechanisms to environmental toxicants by mapping gene expression data of exposure experiments to the resulting model.