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A novel mutation in the myeloperoxidase gene in a Chinese female with complete myeloperoxidase deficiency: The role of nonsense-mediated mRNA decay

Author:
Wang, Kaiyu, Lin, Baoshun, Lin, Jianmin, Lan, Xiaopeng
Source:
Gene 2013 v.515 pp. 205-207
ISSN:
0378-1119
Subject:
biosynthesis, exons, genes, hematologic tests, immune response, innate immunity, messenger RNA, mutation, myeloperoxidase, neutrophils, stop codon
Abstract:
Myeloperoxidase (MPO) is an important enzyme in innate immunity. Here, we describe the first identified Chinese individual with complete MPO deficiency. The proband was ascertained through routine automated complete blood analysis. Analysis of MPO function and immunogenicity revealed that MPO levels in neutrophils were significantly decreased. Mutational analysis revealed a novel premature termination codon p.(Trp602*) in exon 11 of the MPO gene, which was inherited in an autosomal recessive manner. We demonstrated that nonsense-mediated mRNA decay is involved in the molecular pathology of MPO deficiency in this case. The study of MPO deficiency can be helpful in understanding the function and biosynthesis mechanisms of MPO.
Agid:
990267