Department of Dermatology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.
Hum Mutat. 2010 Oct;31(10):E1687-98. doi: 10.1002/humu.21330.
Plectin is a cytoskeletal linker protein which has a long central rod and N- and C-terminal globular domains. Mutations in the gene encoding plectin (PLEC) cause two distinct autosomal recessive subtypes of epidermolysis bullosa: EB simplex (EBS) with muscular dystrophy (EBS-MD), and EBS with pyloric atresia (EBS-PA). Previous studies have demonstrated that loss of full-length plectin with residual expression of the rodless isoform leads to EBS-MD, whereas complete loss or marked attenuation of expression of full-length and rodless plectin underlies the more severe EBS-PA phenotype. However, muscular dystrophy has never been identified in EBS-PA, not even in the severe form of the disease. Here, we report the first case of EBS associated with both pyloric atresia and muscular dystrophy. Both of the premature termination codon-causing mutations of the proband are located within exon 32, the last exon of PLEC. Immunofluorescence and immunoblot analysis of skin samples and cultured fibroblasts from the proband revealed truncated plectin protein expression in low amounts. This study demonstrates that plectin deficiency can indeed lead to both muscular dystrophy and pyloric atresia in an individual EBS patient.
桥粒芯胶蛋白是一种细胞骨架连接蛋白,具有长的中心杆和 N-及 C-末端球状结构域。编码桥粒芯胶蛋白(PLEC)的基因突变导致两种不同的常染色体隐性遗传型大疱性表皮松解症:伴肌营养不良的单纯型大疱性表皮松解症(EBS-MD),和伴幽门闭锁的单纯型大疱性表皮松解症(EBS-PA)。先前的研究表明,全长桥粒芯胶蛋白缺失而残留无杆状结构域的同种型表达导致 EBS-MD,而全长和无杆状桥粒芯胶蛋白的完全缺失或明显衰减则导致更为严重的 EBS-PA 表型。然而,即使是在疾病的严重形式中,EBS-PA 也从未发现过肌营养不良。在这里,我们报告首例与幽门闭锁和肌营养不良相关的 EBS 病例。先证者的两个导致终止密码子提前出现的突变均位于 PLEC 的最后一个外显子 32 中。对先证者的皮肤样本和培养的成纤维细胞进行免疫荧光和免疫印迹分析显示截短的桥粒芯胶蛋白低量表达。本研究表明,桥粒芯胶蛋白缺乏确实可以导致个体 EBS 患者同时出现肌营养不良和幽门闭锁。