TY - JOUR
T1 - HLA-AR, an inactivated antigen-presenting locus related to HLA-A implications for the evolution of the MHC
AU - Zemmour, J.
AU - Koller, B. H.
AU - Ennis, P. D.
AU - Geraghty, D. E.
AU - Lawlor, D. A.
AU - Orr, H. T.
AU - Parham, P.
PY - 1990/5/1
Y1 - 1990/5/1
N2 - The MHC contains many class I genes other than those known to present peptides to T lymphocytes. These additional class I genes vary between species and their functions are unknown. Genes involved in Ag presentation, HLA-A,B,C in humans, are highly diverse whereas other class I genes are of much more limited diversity. We have studied alleles of a gene, HLA-AR, that is closely linked and structurally related to HLA-A; properties consistent with these two loci having been formed by a gene duplication. Compared to HLA-A the diversity in HLA-AR is much less, and does not focus on residues of a putative Ag recognition site. However, the structure of HLA-AR alleles closely resembles those encoding Ag-presenting molecules, although the presence of one or two deleterious mutations prevents these alleles being active in Ag presentation. These results suggest HLA-AR derives from an Ag-presenting locus that became inactivated, possibly as a result of positive natural selection due to changing demands on T cell immunity. Thus absence of diversity may sometimes correlate with loss rather than preservation of function in class I MHC genes.
AB - The MHC contains many class I genes other than those known to present peptides to T lymphocytes. These additional class I genes vary between species and their functions are unknown. Genes involved in Ag presentation, HLA-A,B,C in humans, are highly diverse whereas other class I genes are of much more limited diversity. We have studied alleles of a gene, HLA-AR, that is closely linked and structurally related to HLA-A; properties consistent with these two loci having been formed by a gene duplication. Compared to HLA-A the diversity in HLA-AR is much less, and does not focus on residues of a putative Ag recognition site. However, the structure of HLA-AR alleles closely resembles those encoding Ag-presenting molecules, although the presence of one or two deleterious mutations prevents these alleles being active in Ag presentation. These results suggest HLA-AR derives from an Ag-presenting locus that became inactivated, possibly as a result of positive natural selection due to changing demands on T cell immunity. Thus absence of diversity may sometimes correlate with loss rather than preservation of function in class I MHC genes.
UR - http://www.scopus.com/inward/record.url?scp=0025255539&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0025255539&partnerID=8YFLogxK
M3 - Article
C2 - 2329283
AN - SCOPUS:0025255539
SN - 0022-1767
VL - 144
SP - 3619
EP - 3629
JO - Journal of Immunology
JF - Journal of Immunology
IS - 9
ER -