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RELATIONSHIP BETWEEN DQα AND DQβ RFLP AND CELL SURFACE POLYMORPHISMS OF CLASS II HLA ANTIGENS
Author(s) -
Cascino I.,
Rosenshine S.,
Turco E.,
Marrari M.,
Duquesnoy R. J.,
Trucco M.
Publication year - 1986
Publication title -
international journal of immunogenetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.41
H-Index - 47
eISSN - 1744-313X
pISSN - 1744-3121
DOI - 10.1111/j.1744-313x.1986.tb01124.x
Subject(s) - hla dq , restriction fragment length polymorphism , biology , genetics , restriction enzyme , psti , genomic dna , restriction fragment , allele , microbiology and biotechnology , human leukocyte antigen , major histocompatibility complex , gene , dna , genetic linkage , antigen , haplotype , genotype
SUMMARY DQα and β DNA probes of the human major histocompatibility complex (MHC) were hybridized to restriction enzyme‐digested genomic DNA with the aim of establishing a correspondence between the polymorphisms recognized by classical serology and DNA restriction fragment length polymorphisms (RFLP). In DR homozygous human cell lines, three distinct PstI fragments were recognized by the DQα probe and four PstI fragments were recognized by the DQ β probe. Each fragment was associated with a different group of DR antigens. Three allelic forms of either DXα or β genes were identified, but none showed any strong association with DR or DQ. Family segregation analysis at the DNA level further confirmed the DR linkage of the DQ alleles in estimations of gene frequencies of different alleles of DQα, DQβ, DXα and DXβ. Evidence was presented that the DQα and DQβ allelic forms described at the DNA level correspond to polymorphic determinants at the cell surface which can be defined serologically or in cellular assays. Our data suggest that the HLA‐DQ subregion‐encoded alloantigens should be defined at the individual α and β chain levels.