Computational Identification of Master Regulators Influencing Trypanotolerance in Cattle

Int J Mol Sci. 2021 Jan 8;22(2):562. doi: 10.3390/ijms22020562.

Abstract

African Animal Trypanosomiasis (AAT) is transmitted by the tsetse fly which carries pathogenic trypanosomes in its saliva, thus causing debilitating infection to livestock health. As the disease advances, a multistage progression process is observed based on the progressive clinical signs displayed in the host's body. Investigation of genes expressed with regular monotonic patterns (known as Monotonically Expressed Genes (MEGs)) and of their master regulators can provide important clue for the understanding of the molecular mechanisms underlying the AAT disease. For this purpose, we analysed MEGs for three tissues (liver, spleen and lymph node) of two cattle breeds, namely trypanosusceptible Boran and trypanotolerant N'Dama. Our analysis revealed cattle breed-specific master regulators which are highly related to distinguish the genetic programs in both cattle breeds. Especially the master regulators MYC and DBP found in this study, seem to influence the immune responses strongly, thereby susceptibility and trypanotolerance of Boran and N'Dama respectively. Furthermore, our pathway analysis also bolsters the crucial roles of these master regulators. Taken together, our findings provide novel insights into breed-specific master regulators which orchestrate the regulatory cascades influencing the level of trypanotolerance in cattle breeds and thus could be promising drug targets for future therapeutic interventions.

Keywords: DBP; MYC; animal african trypanosomiasis; master regulators; over-represented pathways.

MeSH terms

  • Animals
  • Cattle
  • Host-Pathogen Interactions / genetics
  • Humans
  • Immunity, Innate / genetics*
  • Immunity, Innate / immunology
  • Liver / metabolism
  • Liver / parasitology
  • Organ Specificity / genetics
  • Proto-Oncogene Proteins c-myc / genetics
  • Spleen / metabolism
  • Spleen / parasitology
  • Trypanosoma / genetics*
  • Trypanosoma / pathogenicity
  • Trypanosomiasis, African / genetics*
  • Trypanosomiasis, African / parasitology
  • Trypanosomiasis, African / transmission
  • Trypanosomiasis, African / veterinary
  • Tsetse Flies / parasitology
  • Tsetse Flies / pathogenicity

Substances

  • Proto-Oncogene Proteins c-myc