Molecular evolution and structural features of IRAK family members

PLoS One. 2012;7(11):e49771. doi: 10.1371/journal.pone.0049771. Epub 2012 Nov 14.

Abstract

The interleukin-1 receptor-associated kinase (IRAK) family comprises critical signaling mediators of the TLR/IL-1R signaling pathways. IRAKs are Ser/Thr kinases. There are 4 members in the vertebrate genome (IRAK1, IRAK2, IRAKM, and IRAK4) and an IRAK homolog, Pelle, in insects. IRAK family members are highly conserved in vertebrates, but the evolutionary relationship between IRAKs in vertebrates and insects is not clear. To investigate the evolutionary history and functional divergence of IRAK members, we performed extensive bioinformatics analysis. The phylogenetic relationship between IRAK sequences suggests that gene duplication events occurred in the evolutionary lineage, leading to early vertebrates. A comparative phylogenetic analysis with insect homologs of IRAKs suggests that the Tube protein is a homolog of IRAK4, unlike the anticipated protein, Pelle. Furthermore, the analysis supports that an IRAK4-like kinase is an ancestral protein in the metazoan lineage of the IRAK family. Through functional analysis, several potentially diverged sites were identified in the common death domain and kinase domain. These sites have been constrained during evolution by strong purifying selection, suggesting their functional importance within IRAKs. In summary, our study highlighted the molecular evolution of the IRAK family, predicted the amino acids that contributed to functional divergence, and identified structural variations among the IRAK paralogs that may provide a starting point for further experimental investigations.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Drosophila melanogaster / genetics
  • Evolution, Molecular*
  • Humans
  • Interleukin-1 Receptor-Associated Kinases / chemistry
  • Interleukin-1 Receptor-Associated Kinases / classification
  • Interleukin-1 Receptor-Associated Kinases / genetics*
  • Models, Molecular
  • Molecular Sequence Data
  • Multigene Family*
  • Phylogeny
  • Protein Conformation
  • Protein Interaction Domains and Motifs
  • Selection, Genetic
  • Sequence Alignment
  • Vertebrates / genetics

Substances

  • Interleukin-1 Receptor-Associated Kinases

Grants and funding

This work was supported by the National Research Foundation of Korea funded by the Ministry of Education, Science, and Technology (2012016803). This work was also partly supported by the Korea Food & Drug Administration (10182KFDA992-2302) and the Priority Research Centers Program (NRF 2010-0028294). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.