The major histocompatibility complex in swine
- 1 February 1999
- journal article
- review article
- Published by Wiley in Immunological Reviews
- Vol. 167 (1) , 179-192
- https://doi.org/10.1111/j.1600-065x.1999.tb01391.x
Abstract
Summary: In swine, the major histocompatibility complex (Mhc) or swine leukocyte antigen (SLA) is located on chromosome 7 and divided by the centromere. Thus, the telomeric class I and more centromeric class III regions are located on the p arm and the class II region is located on the q arm. The SLA region spans about 2 Mb, in which more than 70 genes have so far been characterized. Despite its division by the centromere, the spatial relationships between the genes in the class II and class III regions, and between the well‐conserved non‐class I genes of the class I region, are similar to those found in the human HLA complex. On the other hand, no orthologous relationships have been found between the Mhc class I genes in man and swine. In swine, the 12 SLA class I sequences constitute two distinct clusters. One chister comprises six classical class 1‐related sequences, while the other comprises five class I‐distantly related sequences including two swine homologous genes of the HLA Mhc class I chain‐related gene (MIC) sequence family. The number of functional SLA classical class I genes, as defined by serology, probably varies from one to four, depending on the haplotype. Some of the SLA class I‐distantly related sequences are clearly transcribed. As regards the SLA class II genes, some of them clearly code for at least one functional SLA‐DR and one SLA‐DQ heterodimer product, but none code for any DP product. The amino acid alignment of the variable domains of 33 SLA classical class I chains, and 62 DRβ and 20 DQβ chains confirmed the exceptionally polymorphic pattern of these polypeptides. Among the class II genes, the genes are either monomorphic, like the DRA gene, or oligomorphic, like the DQA genes. In contrast, the DRB and DQB genes display considerable polymorphism, which seems more marked in DRB than DQB genes.Keywords
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