Origins, lineage-specific expansions, and multiple losses of tyrosine kinases in eukaryotes

Mol Biol Evol. 2004 May;21(5):828-40. doi: 10.1093/molbev/msh077. Epub 2004 Feb 12.

Abstract

Tyrosine kinases are important components of metazoan signaling pathways, and their mutant forms are implicated in various malignancies. Searching the sequences from the genomes of 28 eukaryotes and the GenBank, we found tyrosine kinases not only in metazoans but also in the green algae Chlamydomonas reinhardtii, the potato late blight pathogen Phytophthora infestans, and the protozoan pathogen Entamoeba histolytica, contrary to the current view that tyrosine kinases are animal-specific. Based on a phylogenetic analysis, we divided this gene family into 43 subfamilies and found that at least 19 tyrosine kinases were likely present in the common ancestor of chordates, arthropods, and nematodes. Interestingly, most of the subfamilies have conserved domain organizations among subfamily members but have undergone different degrees of expansion during the evolution of metazoans. In particular, a large number of duplications occurred in the lineage leading to the common ancestor of Tagifugu and mammals after its split from the Ciona lineage about 450 to 550 MYA. The timing of expansion coincides with proposed large-scale duplication event in the chordate lineage. Furthermore, gene losses have occurred in most subfamilies. Interestingly, different subfamilies have similar net gain rates in the chordates studied. However, the tyrosine kinases in mouse and human or in fruit fly and mosquito mostly have a one-to-one relationship between species, indicating that static periods of 90 Myr or longer in tyrosine kinase evolution have followed large expansion events.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Cell Lineage
  • Databases as Topic
  • Eukaryota / genetics*
  • Eukaryotic Cells
  • Evolution, Molecular
  • Expressed Sequence Tags
  • Gene Deletion
  • Gene Duplication
  • Genome
  • Humans
  • Mutation
  • Phylogeny
  • Protein Kinases / metabolism
  • Protein-Tyrosine Kinases / genetics*
  • Signal Transduction
  • Species Specificity
  • Time Factors

Substances

  • Protein Kinases
  • Protein-Tyrosine Kinases