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The Journal of Immunology, 1999, 163: 6371-6377.
Copyright © 1999 by The American Association of Immunologists

Characterization of Paired Ig-Like Receptors in Rats1 ,2

Glynn Dennis, Jr.*,{dagger}, Robert P. Stephan*, Hiromi Kubagawa*,{ddagger} and Max D. Cooper3,*,{dagger},||

* Division of Developmental and Clinical Immunology and Departments of {dagger} Microbiology, {ddagger} Pathology, § Pediatrics, and Medicine and || Howard Hughes Medical Institute, University of Alabama, Birmingham, AL 35294

To explore the phylogenetic history of the murine paired Ig-like receptors of activating (PIR-A) and inhibitory (PIR-B) types, we isolated PIR homologues from a rat splenocyte cDNA library. The rat (ra) PIR-A and raPIR-B cDNA sequences predict transmembrane proteins with six highly conserved extracellular Ig-like domains and distinctive membrane proximal, transmembrane, and cytoplasmic regions. The raPIR-B cytoplasmic region contains prototypic inhibitory motifs, whereas raPIR-A features a charged transmembrane region and a short cytoplasmic tail. Southern blot analysis predicts the presence of multiple Pira genes and a single Pirb gene in the rat genome. Although raPIR-A and raPIR-B are coordinately expressed by myeloid cells, analysis of mRNA detected unpaired expression of raPIR-A by B cells and raPIR-B by NK cells. Collectively, these findings indicate that the structural hallmarks of the Pir gene family are conserved in rats and mice, yet suggest divergence of PIR regulatory elements during rodent speciation.




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