KRT6a基因N172del新发突变导致Ⅰ型先天性厚甲症  

A N172del de novo mutation in the KRT6a gene is associated with pachyonychia congenita type Ⅰ

作　　者：王云[1] 林志淼[1] 陈荃[1] 谭燕红[1] 李名扬[1] 杨勇[1] 

机构地区：[1]北京大学第一医院皮肤科,北京100034

出　　处：《中国麻风皮肤病杂志》2012年第8期542-544,共3页China Journal of Leprosy and Skin Diseases

基　　金：国家自然科学基金资助项目(81071289)

摘　　要：目的:检测1例Ⅰ型先天性厚甲症患者KRT6a基因突变。方法:提取该患者及其父母和100名正常对照外周血白细胞基因组DNA,设计针对KRT6a和KRT16基因的特异性引物,PCR扩增KRT6a和KRT16基因的全部外显子,并进行直接测序。结果:PCR扩增结合DNA测序发现该患者KRT6a基因第1外显子存在异常,第514-516位的3个核苷酸AAC缺失,导致第172位氨基酸-天冬酰胺(N)缺失。患者父母及100名正常对照均未发现此突变。未发现KRT16基因突变。结论:KRT6a基因N172del突变可能是导致本例Ⅰ型先天性厚甲症的致病突变,该突变非遗传自父母,为新发突变。Objective： To detect the KRT6a gene mutation in a sporadic Chinese patient with pachyonychia congenital- I （PC- I）. Methods： Genomic DNA was extracted from whole blood by standard method from a male patient with PC- I and his parents. One hundred normal people were used as controls. All the exons of KRT6a and KRT16 genes were amplified by using polymerase chain reaction （PCR） and subjected to automatic DNA sequencing. Results： Direct sequencing of the PCR products revealed a deletion mutation at nucleotide 514 - 516 （514 - 516delAAC） in exon 1 in the patient, leading to the deletion of the amino acid asparagine at cedon 172 located at the start of 1A domain of K6a. No mutation was found in the patient＇ s parents or the controls. No mutation was found in KRT16 gene. Conclusion： A deletion mutation, N172del, has been found in a sporadic Chinese patient with PC- I. The mutation is not inherited from his parents, rather than a de novo mutation.

关 键 词：先天性厚甲症 KRT6a 基因 突变 缺失 

分 类 号：R758.72[医药卫生—皮肤病学与性病学]