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Publication : Molecular cloning, gene structure, and expression pattern of pig immunoreceptor DAP12.

First Author  Yim D Year  2000
Journal  Immunogenetics Volume  51
Issue  6 Pages  436-42
PubMed ID  10866110 Mgi Jnum  J:62569
Mgi Id  MGI:1859099 Doi  10.1007/s002510050642
Citation  Yim D, et al. (2000) Molecular cloning, gene structure, and expression pattern of pig immunoreceptor DAP12. Immunogenetics 51(6):436-42
abstractText  Natural killer (NK) cells express receptors for MHC class I that contain immunoreceptor tyrosine-based inhibitory motif (ITIM) sequences in their cytoplasmic domain. Whereas these receptors inhibit NK cell cytotoxicity, certain isoforms of these NK receptors (e.g., KIR2DS, CD94/NKG2C, and Ly49D) do not have ITIMs, but associate with DAP12 and activate NK cell function. We cloned pig DAP12 cDNA from a pig peripheral blood lymphocyte (PBL) cDNA library using human DAP12 cDNA as a probe. The length of the pig DAP12 cDNA is 526 bp and contains an open reading frame of 324 bp. It has 79% identity with the human DAP12 cDNA sequence in the coding region and 73% identity with mouse DAP12 cDNA. The predicted polypeptide sequence of pig DAP12 is 108 amino acids, being composed of a 23-amino acid leader, a 14-amino acid extracellular domain, a 24-amino acid transmembrane segment, and a 47-amino acid cytoplasmic region. The amino acid sequence of pig DAP12 has 74% and 71% sequence identity with human DAP12 and mouse DAP12, respectively. Pig DAP12 has a conserved aspartic acid in the transmembrane region, and two conserved cysteine residues in the extracellular domain. It also contains an immunoreceptor tyrosine-based activation motif sequence in the cytoplasmic region. Genomic organization reveals that pig DAP12 consists of five exons and four introns. Southern blot analysis of pig genomic DNA revealed that DAP12 is a single-copy gene. In Northern blot analysis, DAP12 transcripts were detected in spleen, liver, thymus, and lymph node. DAP12 transcripts are expressed not only in PBLs, but also in granulocytes, macrophages, and monocytes.
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