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Publication : Cloning and characterization of the bovine MHC class I-like Fc receptor.

First Author  Kacskovics I Year  2000
Journal  J Immunol Volume  164
Issue  4 Pages  1889-97
PubMed ID  10657638 Mgi Jnum  J:60330
Mgi Id  MGI:1353176 Doi  10.4049/jimmunol.164.4.1889
Citation  Kacskovics I, et al. (2000) Cloning and characterization of the bovine MHC class I-like Fc receptor. J Immunol 164(4):1889-97
abstractText  In the cow, maternal immunity is exclusively mediated by colostral Igs, but the receptor responsible for the IgG transport has not yet been identified. 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. We now report the cloning and characterization of the bovine FcRn (bFcRn). The cDNA and deduced amino acid sequences show high similarity to the FcRn in other species, and it consists of three extracellular domains, a hydrophobic transmembrane region, and a cytoplasmic tail. Despite the high similarity of the extracellular domains with other species, the bovine cytoplasmic tail is the shortest thus far analyzed. Aligning the known FcRn sequences, we noted that the bovine protein shows a 3-aa deletion compared to the rat and mouse sequences in the alpha1 loop. Furthermore, we found a shorter transcript of the bFcRn reflecting an exon 6-deleted mRNA, which results from an inadequate splice acceptor site in intron 5 and produces a transmembrane-deficient molecule, as was previously demonstrated in the related MHC class I gene family in mouse and humans. The presence of bFcRn transcripts in multiple tissues, including the mammary gland, suggests their involvement both in IgG catabolism and transcytosis.
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