HLA-DRB INTRON-1 SEQUENCES - IMPLICATIONS FOR THE EVOLUTION OF HLA-DRB GENES AND HAPLOTYPES

Citation
Y. Satta et al., HLA-DRB INTRON-1 SEQUENCES - IMPLICATIONS FOR THE EVOLUTION OF HLA-DRB GENES AND HAPLOTYPES, Human immunology, 51(1), 1996, pp. 1-12
Citations number
40
Categorie Soggetti
Immunology
Journal title
ISSN journal
01988859
Volume
51
Issue
1
Year of publication
1996
Pages
1 - 12
Database
ISI
SICI code
0198-8859(1996)51:1<1:HIS-IF>2.0.ZU;2-0
Abstract
Human DRB genes encode beta chains of the major histocompatibility com plex (MHC) class II molecules. Although nine DRB loci have been mapped to the short arm of chromosome 6, an individual chromosome contains o nly one to five loci and is classified into one of five major haplotyp es. To elucidate the origin of human DRB loci and haplotypes, intron 1 sequences approximately 5000 bp in length were determined for three D RB1 alleles (DRB103, DRB1*04, and DRB1*15) and five DRB genes (DRB2, DRB3, DRB4, DRB5, and DRB7). The sequences were subjected to phylogene tic analyses together with previously determined intron 4 and 5 sequen ces. The sequences provided two sources of information: Nucleotide sub stitutions that could be used to construct phylogenetic trees and to e stimate divergence times and a set of insertions (mostly Alu elements) chat reveal the order of splitting of duplicated genes. The combined data indicate that the ancestor of the human DRB genes was HLA-DRB104 -like and that the DRB2, DRB7, DRB5, and DRB3 genes arose from this an cestor by four rounds of duplication 58, 56, 53, and 36 million years (MY) ago, respectively. The DRB4 gene may have arisen 46 MY ago by a d eletion from the DRB1 and DRB2 genes and the DRB6 gene is probably an allele at the DRB2 locus. During the course of its evolution, the DRB1 04 gene acquired an intron 1 segment (including two Alu elements) fro m a gene that became the ancestor of DRB103. The present-day HLA-DR h aplotypes were derived from three principal ancestral haplotypes: DRB1 -DRB2, DRB1-DRB5, and DRB1-DRB7. (C) American Society for Histocompati bility and Immunogenetics, 1996.