Characterization of LMP polymorphism in homozygous typing cells and a random population

• Published in: Human immunology Vol. 60; no. 2; pp. 145 - 151
• Main Authors: Lim, Jean K, Hunter, Jay, Fernandez-Vina, Marcelo, Mann, Dean L
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.02.1999
• Subjects: Cysteine Endopeptidases; Haplotypes; HLA class II; HTC; Humans; LMP2; LMP7; Major Histocompatibility Complex - genetics; Multienzyme Complexes; polymorphism; Polymorphism, Genetic; Proteasome Endopeptidase Complex; Proteins - genetics; LMP2; β2M; TAP; TCR; ARMS; MHC; polymorphism; LMP7; LMP; IFN; HTC; HLA class II; HLA; PCR
• ISSN: 0198-8859; 1879-1166
• DOI: 10.1016/S0198-8859(98)00106-2

Within the class II region of the MHC are several genes whose products are involved in processing antigen for HLA class I presentation. Two such genes, LMP2 and LMP7, encode products that are incorporated into a multicatalytic proteinase complex which serves as the major pathway for protein degradation for class I peptide presentation. Polymorphic residues have been identified in both LMP2 and LMP7. In this report, we describe an ARMS-PCR method to distinguish LMP7 alleles. We applied this method to characterize these alleles in addition to LMP2 alleles in 50 homozygous typing cells (HTC) as well as in a panel of 110 random individuals. Of the four possible combinations of LMP2 and LMP7, we observed three in the HTC population, while all four were observed in the random population. The frequencies at which allele combinations were observed were similar to that predicted by individual allele frequencies. We also analyzed the possibility of linkage disequilibrium of LMP2 and LMP7 alleles with TAP1, TAP2, and specific HLA class I alleles in both populations. From this data, there seems to be no apparent linkage disequilibrium and no indication that particular combinations of LMP2 and LMP7 have been maintained.