A novel homozygous stop-codon mutation in human HFE responsible for nonsense-mediated mRNA decay

Maria Carmela Padula, Giuseppe Martelli, Marilena Larocca, Rocco Rossano, Attilio Olivieri

Research output: Contribution to journalArticlepeer-review

Abstract

HFE-hemochromatosis (HH) is an autosomal disease characterized by excessive iron absorption. Homozygotes for H63D variant, and still less H63D heterozygotes, generally do not express HH phenotype. The data collected in our previous study in the province of Matera (Basilicata, Italy) underlined that some H63D carriers showed altered iron metabolism, without additional factors. In this study, we selected a cohort of 10/22 H63D carriers with severe biochemical iron overload (BIO). Additional analysis was performed for studying HFE exons, exon-intron boundaries, and untranslated regions (UTRs) by performing DNA extraction, PCR amplification and sequencing. The results showed a novel substitution (NM_000410.3:c.847C>T) in a patient exon 4 (GenBankJQ478433); it introduces a premature stop-codon (PTC). RNA extraction and reverse-transcription were also performed. Quantitative real-time PCR was carried out for verifying if our aberrant mRNA is targeted for nonsense-mediated mRNA decay (NMD); we observed that patient HFE mRNA was expressed much less than calibrator, suggesting that the mutated HFE protein cannot play its role in iron metabolism regulation, resulting in proband BIO. Our finding is the first evidence of a variation responsible for a PTC in iron cycle genes. The genotype-phenotype correlation observed in our cases could be related to the additional mutation.

Original languageEnglish
Pages (from-to)138-143
Number of pages6
JournalBlood cells, molecules & diseases
Volume53
Issue number3
DOIs
Publication statusPublished - 2014

Keywords

  • Hemochromatosis
  • HFE
  • Mutations
  • Nonsense-mediated mRNA decay (NMD)
  • Premature translation-termination codon (PTC)

ASJC Scopus subject areas

  • Molecular Biology
  • Molecular Medicine
  • Hematology
  • Cell Biology
  • Medicine(all)

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