Identification of immune-relevant genes in histoincompatible rejecting colonies of the tunicate Botryllus schlosseri

Dev Comp Immunol. 2007;31(9):889-902. doi: 10.1016/j.dci.2006.12.009. Epub 2007 Jan 24.

Abstract

The colonial ascidian Botryllus schlosseri manifests a unique allorecognition system that is controlled by a single histocompatibility haplotype, the Fu/HC locus. When two allogeneic incompatible colonies come into direct contact, they develop inflammatory-like rejection lesions, called points of rejection (POR). While screening for differentially expressed genes during POR formation, we developed and analyzed a cDNA library of expressed sequence tags (ESTs) with 1693 unique ESTs that were clustered and assembled into 217 contigs and 1476 singlets. About 51% of these ESTs showed high similarity (E-value 0.005) to known database sequences, of which 123 matches were identified as immune-relevant genes encoding for stress proteins, pattern recognition receptors and complement proteins, proteases and protease inhibitors, cell adhesion and coagulation proteins, cytokine-related proteins, programmed cell death and proteasome-associated proteins. This first EST wide-screening analysis of the Botryllus allorecognition effector arm reveals a complex innate immune system, hallmarked by a whole genome response to allorecognition challenge.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Apoptosis / genetics
  • Base Sequence
  • Blood Coagulation / genetics
  • Cell Adhesion
  • Cytokines / genetics
  • DNA, Complementary / genetics
  • Databases, Nucleic Acid
  • Expressed Sequence Tags
  • Gene Expression Regulation / genetics*
  • Heat-Shock Proteins / genetics
  • Histocompatibility Antigens / genetics*
  • Histocompatibility Antigens / immunology*
  • Lectins / genetics
  • Neoplasm Proteins / genetics
  • Peptide Hydrolases / genetics
  • Protease Inhibitors / metabolism
  • Urochordata / cytology
  • Urochordata / genetics*
  • Urochordata / immunology*

Substances

  • Cytokines
  • DNA, Complementary
  • Heat-Shock Proteins
  • Histocompatibility Antigens
  • Lectins
  • Neoplasm Proteins
  • Protease Inhibitors
  • Peptide Hydrolases