Literature DB >> 2478623

Molecular analysis of the serologically defined HLA-Aw19 antigens. A genetically distinct family of HLA-A antigens comprising A29, A31, A32, and Aw33, but probably not A30.

K Kato1, J A Trapani, J Allopenna, B Dupont, S Y Yang.   

Abstract

The HLA-Aw19 complex consists of a number of serologically cross-reactive Ag (i.e., A29, A30, A31, A32, and Aw33) which exhibit an epitope shared by HLA-B and -C proteins. To investigate the structural basis for these serologic cross-reactivities, we have cloned and determined the nucleotide sequences for A30, A31, and Aw33, and compared the predicted amino acid sequences with those already available for A29, A32, and other class I allelic products. All alleles of the Aw19 group contained A-locus-specific sequences, exhibiting "A-ness." The structural similarities between Aw19 polypeptides were found in the alpha 1 and alpha 2 domains, where shared amino acid residues were identified that correlated with observed serological reactivity patterns. Seven Aw19-specific nucleotides were found. Two of these were silent substitutions, but the remaining five resulted in Aw19-specific amino acid residues. Each of the HLA-A alleles can be classified into one of the five serologically cross-reacting groups. In the Aw19 group, the alleles A29, A31, A32, and Aw33 are closely related serologically as well as genetically whereas A30 probably belongs to the A1/A3/A11 group. The similarity between A30 and the other Aw19 alleles may have resulted from two independent gene conversions affecting exons 2 and 3. Additional mutations or gene conversion-like events in A30 were also noted. It is postulated that gene conversions have played a significant role in the divergence of the Aw19 alleles. However, each serologically cross-reactive Aw19 allotype appears to have arisen directly from a common ancestral allele. A30 was the only exception, and this allele may represent an unusual allotype, which is subject to a high rate of genetic changes, as is seen in the H-2Kb gene of the mouse.

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Year:  1989        PMID: 2478623

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  21 in total

1.  Polymorphic specificity of Q1/28, a monoclonal antibody that preferentially reacts with free class I heavy chains.

Authors:  R J Benjamin; J R Abrams; J R Parnes; J A Madrigal; P Parham
Journal:  Immunogenetics       Date:  1992       Impact factor: 2.846

2.  Patterns of nucleotide substitutions inferred from the phylogenies of the class I major histocompatibility complex genes.

Authors:  T Imanishi; T Gojobori
Journal:  J Mol Evol       Date:  1992-09       Impact factor: 2.395

3.  Structure of the HLA-A*0211 (A2.5) subtype: further evidence for selection-driven diversification of HLA-A2 antigens.

Authors:  A R Castaño; J A López de Castro
Journal:  Immunogenetics       Date:  1992       Impact factor: 2.846

4.  Classification of A1- and A24-supertype molecules by analysis of their MHC-peptide binding repertoires.

Authors:  John Sidney; Scott Southwood; Alessandro Sette
Journal:  Immunogenetics       Date:  2005-07-08       Impact factor: 2.846

5.  HLA-A29 subtypes and birdshot chorioretinopathy.

Authors:  L P de Waal; N M Lardy; A R van der Horst; G S Baarsma; A Kijlstra; L Noens; H A Priem
Journal:  Immunogenetics       Date:  1992       Impact factor: 2.846

6.  Molecular definition of an elusive third HLA-A9 molecule: HLA-A9.3.

Authors:  A M Little; J A Madrigal; P Parham
Journal:  Immunogenetics       Date:  1992       Impact factor: 2.846

7.  Segmental exchange between MHC class I genes in a higher primate: recombination in the gorilla between the ancestor of a human non-functional gene and an A locus gene.

Authors:  D I Watkins; Z W Chen; T L Garber; A L Hughes; N L Letvin
Journal:  Immunogenetics       Date:  1991       Impact factor: 2.846

8.  The peptide-binding specificity of HLA-A*3001 demonstrates membership of the HLA-A3 supertype.

Authors:  Kasper Lamberth; Gustav Røder; Mikkel Harndahl; Morten Nielsen; Claus Lundegaard; Claus Schafer-Nielsen; Ole Lund; Soren Buus
Journal:  Immunogenetics       Date:  2008-09-04       Impact factor: 2.846

9.  Mhc-A locus molecules in pygmy chimpanzees: conservation of peptide pockets.

Authors:  D A Lawlor; B T Edelson; P Parham
Journal:  Immunogenetics       Date:  1995       Impact factor: 2.846

10.  The MHC E locus in macaques is polymorphic and is conserved between macaques and humans.

Authors:  J E Boyson; S N McAdam; A Gallimore; T G Golos; X Liu; F M Gotch; A L Hughes; D I Watkins
Journal:  Immunogenetics       Date:  1995       Impact factor: 2.846

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