Identification of novel non-HFE mutations in Chinese patients with hereditary hemochromatosis.

Abstract

BACKGROUNDS:

Hereditary hemochromatosis (HH) is mainly caused by homozygous p.C282Y mutations in HFE in the Caucasians. We recently reported non-HFE mutations constitute the major cause of HH in Chinese. However, there is still a relatively high proportion of cases with primary iron overload from unexplained causes. We aimed to explore novel non-HFE mutations in Chinese patients with primary iron overload.

METHODS:

Whole exome sequence was conducted to screen mutations in novel HH-related genes in the 9 cases with unexplained primary iron overload. Then the representative candidate genes were screened for mutations in another cohort of 18 HH cases. The biological function of the selected genes and variants were analyzed in vitro.

RESULTS:

Whole exome sequencing of 9 cases with unexplained primary iron overload identified 42 missense variants in 40 genes associated with iron metabolism pathway genes such as UBE2O p.K689R and PCSK7 p.R711W. Subsequent Sanger sequencing of the UBE2O and PCSK7 genes in the 27 cases with primary iron overload identified p.K689R in UBE2O, p.R711W and p.V143F in PCSK7 at frequency of 2/27,1/27 and 2/27 respectively. In vitro siRNA interference of UBE2O and PCSK7 resulted in down-regulated HAMP mRNA expression. Adenovirus generation of UBE2O p.K689R in cell lines resulted in increased expression of SMAD6 and SMAD7 and downregulation of p-SMAD1/5 and HAMP expression, and the reduction of hepcidin level.

CONCLUSIONS:

Our study identified a series of novel candidate non-HFE mutations in Chinese patients with HH. These may provide insights into the genetic basis of unexplained primary iron overload.

• Authors: Wei Zhang, Yanmeng Li, Anjian Xu, Qin Ouyang, Liyan Wu, Donghu Zhou, Lina Wu, Bei Zhang, Xinyan Zhao, Yu Wang, Xiaoming Wang, Weijia Duan, Qianyi Wang, Hong You, Jian Huang, Xiaojuan Ou, Jidong Jia, China Registry of Genetic/Metabolic Liver Diseases (CR-GMLD) Group
• Journal: Orphanet journal of rare diseases (Orphanet J Rare Dis) Vol. 17 Issue 1 Pg. 216 (06 06 2022) ISSN: 1750-1172 [Electronic] England
• PMID: 35668470 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: © 2022. The Author(s).

Chemical References

• Hemochromatosis Protein
• Histocompatibility Antigens Class I
• Membrane Proteins
• Ubiquitin-Conjugating Enzymes
• UBE2O protein, human
• PCSK7 protein, human
• Subtilisins

Topics

• China
• Hemochromatosis (genetics)
• Hemochromatosis Protein (genetics)
• Histocompatibility Antigens Class I (genetics)
• Humans
• Iron Overload (genetics)
• Membrane Proteins (genetics)
• Mutation (genetics)
• Subtilisins (genetics)
• Ubiquitin-Conjugating Enzymes (genetics)