Allelic diversity at class II DRB1 and DQB loci of the pig MHC (SLA)
Citation
Th. Kanai et al., Allelic diversity at class II DRB1 and DQB loci of the pig MHC (SLA), IMMUNOGENET, 50(5-6), 1999, pp. 295-300
Categorie Soggetti
Immunology
Journal title
IMMUNOGENETICS
SICI code
0093-7711(199912)50:5-6<295:ADACID>2.0.ZU;2-V
Abstract
The loci encoding the beta chain of the pig major histocompatibility comple
x (MHC) class II antigens, SLA-DR and -DQ, have been known to exhibit a rem
arkable degree of allelic polymorphism. Here, to understand the generation
of SLA class II polymorphism, 25 SLA-DRB1 and 24 SLA-DQB genes including ne
wly identified 12 SLA-DRB1 and 7 SLA-DQB genes obtained from miniature pigs
were analyzed based on the nucleotide and deduced amino acid sequences. Mo
st of the allelic diversity was attributed to the variable sequences which
encode a beta(1) domain consisting of a beta-pleated sheet followed by an a
lpha helix. In the beta(1) domain coding region, there were four GC-rich se
quences, which have been considered to involve the intra-exon sequence exch
ange also in other gene evolutions. The first and second GC-rich sequences
were X-like sequences, which have been shown to be a putative recombination
signal, and were stably conserved among SLA-DRB1 and DQB genes. These X-li
ke sequences identified in SLA-DRB1 and SLA-DQB were found to encode the fi
rst turning point of the beta-pleated sheet and the boundary between the be
ta-pleated sheet and the alpha helix. Analysis of clustered sequence variat
ion also suggested intra-exon gene conversions in which the chi-like sequen
ces act as putative breakpoints. In addition to point mutations and selecti
on mechanism, intra-exon gene conversions must be an important mechanism in
the generation of allelic polymorphism at the SLA-DRB1 and SLA-DQB.