Isolation of the gene encoding the bovine neonatal Fc receptor

Vet Immunol Immunopathol. 2005 Oct 18;108(1-2):145-50. doi: 10.1016/j.vetimm.2005.07.007.

Abstract

The role of an IgG-Fc receptor (FcRn) that resembles a class I MHC Ag in transporting IgGs through epithelial cells was recently shown in selected species. Here we report our preliminary characterization of a clone encoding the alpha chain of the bovine FcRn from a BAC library. The recombinant BAC DNA was digested, analyzed by Southern blot hybridization and a bovine FcRn positive 9 kb long fragment was subcloned and partially sequenced. The exon/intron organization of the bovine FcRn alpha chain gene was deduced by comparison with its cDNA sequence. The sequence revealed a similar organization to the human and mouse FcRn alpha chain genes. The bovine FcRn alpha chain gene has acquired several repetitive sequences in its 5'-flanking region, including multiple SINE and LINE elements. Potential binding sites for transcription factors within the 5'-flanking sequence were identified using TESS and TFSEARCH programs. The 5'-flanking region of the bFcRn alpha chain gene was analyzed for its ability to directly express the luciferase reporter gene in bovine mammary gland epithelial cells. Transient transfection of a luciferase construct revealed that there was promoter activity in the region -1787 to +92 of the 5'-flanking sequence.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Animals, Newborn
  • Binding Sites / genetics
  • Cattle
  • Cell Line
  • Cloning, Molecular
  • DNA / genetics
  • DNA / metabolism
  • Exons
  • Female
  • Genes, Reporter
  • Histocompatibility Antigens Class I / genetics*
  • Histocompatibility Antigens Class I / metabolism
  • Humans
  • Immunity, Mucosal
  • Introns
  • Long Interspersed Nucleotide Elements
  • Mammary Glands, Animal / immunology
  • Mice
  • Receptors, Fc / genetics*
  • Receptors, Fc / metabolism
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Short Interspersed Nucleotide Elements
  • Transcription Factors / metabolism
  • Transfection

Substances

  • Histocompatibility Antigens Class I
  • Receptors, Fc
  • Recombinant Proteins
  • Transcription Factors
  • DNA
  • Fc receptor, neonatal