Yotsumoto S, Akiyama M, Yoneda K, Fukushige T, Kobayashi K, Saheki T, Kanzaki T
Department of Dermatology, Faculty of Medicine, Kagoshima University, 8-35-1 Sakuragaoka, 890-8520, Kagoshima, Japan.
J Dermatol Sci. 2000 Nov;24(2):119-25. doi: 10.1016/s0923-1811(00)00087-6.
We described a Japanese female with lamellar ichthyosis whose transglutaminase 1 gene (TGM1 gene) was mutated. DNA sequence analysis revealed that the patient had a homozygous mutation, i.e. a point mutation from G to A at nucleotide 1494 resulting in the substitution of glycine for arginine at codon 143. Her mother was heterozygous for this mutation. In situ transglutaminase assay in the patient's skin showed loss of enzyme activity. Ultrastructural examination revealed incomplete formation of cornified cell envelopes and electron-dense materials adjacent to plasma membranes. These results suggest that defective transglutaminase activity caused by homozygous TGM1 gene mutation (G143R) results in disruption of cornified envelope assembly and the clinical phenotype of lamellar ichthyosis.
我们描述了一名患有板层状鱼鳞病的日本女性,其转谷氨酰胺酶1基因(TGM1基因)发生了突变。DNA序列分析显示,该患者存在纯合突变,即在核苷酸1494处由G突变为A的点突变,导致密码子143处的精氨酸被甘氨酸取代。她的母亲是该突变的杂合子。对患者皮肤进行的原位转谷氨酰胺酶检测显示酶活性丧失。超微结构检查发现角质化细胞包膜形成不完全,且质膜附近有电子致密物质。这些结果表明,纯合TGM1基因突变(G143R)导致的转谷氨酰胺酶活性缺陷会导致角质化包膜组装破坏以及板层状鱼鳞病的临床表型。