Two novel mutations of the ATP2C1 gene in Chinese patients with Hailey-Hailey disease

• Published in: Archives of Dermatological Research Vol. 299; no. 4; pp. 209 - 211
• Main Authors: Li, Xiaoli, Xiao, Shengxiang, Peng, Zhenhui, Liu, Yan, Wang, Junmin, Zhou, Xin
• Format: Journal Article
• Language: English
• Published: Berlin Springer 01.07.2007; Springer Nature B.V
• Subjects: Adult; Asian Continental Ancestry Group - genetics; Biological and medical sciences; Bullous diseases of the skin; Calcium-Transporting ATPases - genetics; Dermatology; Exons; Heterozygote; Humans; Male; Medical sciences; Middle Aged; Mutation, Missense - genetics; Pedigree; Pemphigus, Benign Familial - ethnology; Pemphigus, Benign Familial - genetics; Pemphigus, Benign Familial - pathology; Skin - pathology; Asia; China; Bullous dermatosis; Human; Skin disease; Hailey Hailey disease; Gene; Dermatology; ATP2C1 gene; Chinese; Genetics; Mutation; Hailey-Hailey disease; Genetic disease
• ISSN: 0340-3696; 1432-069X
• DOI: 10.1007/s00403-007-0761-x

Hailey-Hailey disease (HHD; OMIM 169600) is an autosomal dominant blistering disease. Pathogenic mutations in ATP2C1 encoding the human secretory pathway Ca(2+)/Mn(2+)-ATPase protein 1 (hSPCA1) have been identified since 2000. The aim of this study was to report a Chinese pedigree and a sporadic case of HHD and to explore the genetic mutations. The Chinese pedigree and the sporadic case of typical HHD were subjected to mutation detection of ATP2C1. The 27 coding exons and their flanking sequences were amplified and sequenced. The heterozygous C to T transition at nucleotide 2753 in exon 26 and G to T transition at nucleotide 2090 in exon 21 of the ATP2C1 gene were identified in a pedigree and a sporadic case of HHD, respectively. The C2753T transition resulted in a novel nonsense mutation of glutamine codon (CAG) to a stop codon (TAG) at amino acid residue 865 (Q865X) and the G2090T transition resulted in a novel missense mutation of glycine condon (GGA) to Valine (GUA) at amino acid residue 645 (G645V) in hSPCA1. This study should be useful for genetic counseling and prenatal diagnosis for affected families and in expanding the repertoire of ATP2C1 mutations underlying HHD.