HLA-H and associated proteins in patients with hemochromatosis

Abstract

Background: The 845A(C282Y) mutation in the HLA-H gene accounts for most cases of hereditary hemochromatosis in patients who are of European origin. Some lack this mutation, however, and it is not present in Asian patients. Thus, other mutations either in HLA-H or associated proteins may be present in such patients. HLA-H associates with β-2-microgiobulin. Calreticulin associates with class 1 HLA proteins and appears to be identical with mobilferrin, a putative iron transport protein. These two proteins are therefore candidates for mutations in patients with hemochromatosis. Materials and Methods: We have sequenced the coding region and parts of introns of the HLA-H gene, the β-2-microglobulin gene, and the calreticulin (mobilferrin) gene of 10, 7, and 5 hemochromatosis patients, respectively, selecting those who were not homozygous for the 845A(C282Y) mutation. The number of chromosomes at risk studied were 18 for HLA-H, 14 for β-2- microglobulin, and 10 for calreticulin. Results: We detected 3 new intronic polymorphisms in the HLA-H gene, each a point mutation. Some differences from published sequences of β-2-microgiobulin and calreticulin were documented, but these were uniformly present in all samples. Conclusions: The lack of additional mutations in the HLA-H gene is remarkable, and we speculate that the C282Y mutation may be a gain-of-function change.