Abnormal regulation of HFE mRNA expression may not contribute to primary iron overload

E. Vercesi, P. Cerani, V. Rolandi, A. Rovati, G. Bergamaschi

Research output: Contribution to journalArticlepeer-review

Abstract

Background and Objectives. Hereditary hemochromatosis (HHC) is a common, recessively inherited, genetic disorder associated with an abnormality of the HFE gene. Subjects homozygous for a point mutation in the gene coding sequence, leading to the amino acid substitution C282Y, are usually affected by the disease. A second point mutation, causing the amino acid substitution H63D, has been described, and compound heterozygotes for the two mutations or homozygotes for the H63D mutation are at risk of developing a mikler form of HHC. In populations of northern European origin the C282Y substitution accounts for more than 90% of cases of HHC. In Italy, however, fewer than 70% of patients with HHC are homozygous or compound heterozygous for HFE mutations. Even in the absence of muttons in its coding region, the HFE gene might be involved in the pathogenesis of HHC through inhibition of transcription of the gene or reduced stability of its mRNA. Design and Methods. Since little is known about the regulation of HFE expression, we investigated. 17 subjects heterozygous for one of the HFE mutations and with biochemical evidence of iron overload and compared the levels of wild type and mutated mRNAs in their peripheral blood cells. c-DNA regions flanking the mutated codons were amplified by reverse transcriptase polymerase chain reaction (PCR). PCR products derived from the two alleles were differentiated and quantified by digestion with restriction enzymes, electrophoresis in an agarose gel stained with ethldium bromide and densitometric scanning of the gel. Results. In all cases wild type and mutated mRNAs were expressed at similar levels, suggesting that reduced expression of an HFE allele coding a nodal protein is not involved in the pathogenesis of iron overload. However, we can not rule out that a tissue specific regulation of HFE expression in the cells directly involved in iron absorption is altered and contributes to the pathogenesis of the disease. Interpretation and Conclusions. Our results suggest that primary iron overload is a multigenic syndrome; this hypothesis is strongly supported by the recent demonstration that the juvenile hemochromatosis locus maps to human chromosome 1q. (C) 2000, Ferrata Storti Foundation.

Original languageEnglish
Pages (from-to)787-791
Number of pages5
JournalHaematologica
Volume85
Issue number8
Publication statusPublished - 2000

Keywords

  • Coding sequence
  • Hereditary hemochromatosis (HHC)
  • HFE mRNA
  • Point mutations
  • RT-PCR

ASJC Scopus subject areas

  • Hematology

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