Genomic analysis of immunity in a Urochordate and the emergence of the vertebrate immune system: "waiting for Godot"

Immunogenetics. 2003 Nov;55(8):570-81. doi: 10.1007/s00251-003-0606-5. Epub 2003 Oct 7.

Abstract

Genome-wide sequence analysis in the invertebrate chordate, Ciona intestinalis, has provided a comprehensive picture of immune-related genes in an organism that occupies a key phylogenetic position in vertebrate evolution. The pivotal genes for adaptive immunity, such as the major histocompatibility complex (MHC) class I and II genes, T-cell receptors, or dimeric immunoglobulin molecules, have not been identified in the Ciona genome. Many genes involved in innate immunity have been identified, including complement components, Toll-like receptors, and the genes involved in intracellular signal transduction of immune responses, and show both expansion and unexpected diversity in comparison with the vertebrates. In addition, a number of genes were identified which predicted integral membrane proteins with extracellular C-type lectin or immunoglobulin domains and intracellular immunoreceptor tyrosine-based inhibitory motifs (ITIMs) and immunoreceptor tyrosine-based activation motifs (ITAMs) (plus their associated signal transduction molecules), suggesting that activating and inhibitory receptors have an MHC-independent function and an early evolutionary origin. A crucial component of vertebrate adaptive immunity is somatic diversification, and the recombination activating genes (RAG) and activation-induced cytidine deaminase (AID) genes responsible for the Generation of diversity are not present in Ciona. However, there are key V regions, the essential feature of an immunoglobulin superfamily VC1-like core, and possible proto-MHC regions scattered throughout the genome waiting for Godot.

MeSH terms

  • Animals
  • Antigen Presentation / genetics
  • Ciona intestinalis / genetics*
  • Ciona intestinalis / immunology*
  • Cytokines / physiology
  • Genes, MHC Class I / physiology
  • Genes, MHC Class II / physiology
  • Genome
  • Immunity, Innate / genetics
  • Membrane Glycoproteins / physiology
  • Phagocytosis
  • Receptors, Cell Surface / physiology
  • Signal Transduction
  • Toll-Like Receptors

Substances

  • Cytokines
  • Membrane Glycoproteins
  • Receptors, Cell Surface
  • Toll-Like Receptors