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Human pathways in animal models: possibilities and limitations.
Doncheva, Nadezhda T; Palasca, Oana; Yarani, Reza; Litman, Thomas; Anthon, Christian; Groenen, Martien A M; Stadler, Peter F; Pociot, Flemming; Jensen, Lars J; Gorodkin, Jan.
Affiliation
  • Doncheva NT; Center for non-coding RNA in Technology and Health, University of Copenhagen, 1871 Frederiksberg, Denmark.
  • Palasca O; Department of Veterinary and Animal Sciences, University of Copenhagen, 1870 Frederiksberg, Denmark.
  • Yarani R; Novo Nordisk Foundation Center for Protein Research, University of Copenhagen, 2200 Copenhagen, Denmark.
  • Litman T; Center for non-coding RNA in Technology and Health, University of Copenhagen, 1871 Frederiksberg, Denmark.
  • Anthon C; Department of Veterinary and Animal Sciences, University of Copenhagen, 1870 Frederiksberg, Denmark.
  • Groenen MAM; Novo Nordisk Foundation Center for Protein Research, University of Copenhagen, 2200 Copenhagen, Denmark.
  • Stadler PF; Translational Type 1 Diabetes Research, Steno Diabetes Center Copenhagen, 2820 Gentofte, Denmark.
  • Pociot F; Department of Immunology and Microbiology, University of Copenhagen, 2200 Copenhagen, Denmark.
  • Jensen LJ; Exploratory Biology, LEO Pharma A/S, 2750 Ballerup, Denmark.
  • Gorodkin J; Center for non-coding RNA in Technology and Health, University of Copenhagen, 1871 Frederiksberg, Denmark.
Nucleic Acids Res ; 49(4): 1859-1871, 2021 02 26.
Article in En | MEDLINE | ID: mdl-33524155
ABSTRACT
Animal models are crucial for advancing our knowledge about the molecular pathways involved in human diseases. However, it remains unclear to what extent tissue expression of pathways in healthy individuals is conserved between species. In addition, organism-specific information on pathways in animal models is often lacking. Within these limitations, we explore the possibilities that arise from publicly available data for the animal models mouse, rat, and pig. We approximate the animal pathways activity by integrating the human counterparts of curated pathways with tissue expression data from the models. Specifically, we compare whether the animal orthologs of the human genes are expressed in the same tissue. This is complicated by the lower coverage and worse quality of data in rat and pig as compared to mouse. Despite that, from 203 human KEGG pathways and the seven tissues with best experimental coverage, we identify 95 distinct pathways, for which the tissue expression in one animal model agrees better with human than the others. Our systematic pathway-tissue comparison between human and three animal modes points to specific similarities with human and to distinct differences among the animal models, thereby suggesting the most suitable organism for modeling a human pathway or tissue.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Models, Animal Limits: Animals / Humans Language: En Journal: Nucleic Acids Res Year: 2021 Document type: Article Affiliation country: Denmark

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Models, Animal Limits: Animals / Humans Language: En Journal: Nucleic Acids Res Year: 2021 Document type: Article Affiliation country: Denmark