Shen Chao, Wang Jingbing, Wu Xiaotang, Wang Fuchao, Liu Yang, Guo Xiaoying, Zhang Lina, Cao Yanfei, Cao Xiuhua, Ma Hongxing
Department of Clinical Diagnosis, General Hospital of Daqing Oil Field, Daqing, Heilongjiang Province, People's Republic of China.
Department of Ophthalmology, General Hospital of Daqing Oil Field, Daqing, Heilongjiang Province, People's Republic of China.
BMC Ophthalmol. 2017 May 19;17(1):73. doi: 10.1186/s12886-017-0476-5.
Congenital cataract is the most frequent cause of blindness during infancy or early childhood. To date, more than 40 loci associated with congenital cataract have been identified, including at least 26 genes on different chromosomes associated with inherited cataract. This present study aimed to identify the genetic mutation in a six-generation Chinese family affected with congenital cataract.
A detailed six-generation Chinese cataract family history and clinical data of the family members were recorded. A total of 27 family members, including 14 affected and 13 unaffected individuals were recruited. Whole exome sequencing was performed to determine the disease-causing mutation. Sanger sequencing was used to confirm the results.
A known missense mutation, c. 139G > A (p. D47N), in Cx50 was identified. This mutation co-segregated with all affected individuals and was not observed in the unaffected family members or in 100 unrelated controls. The homology modeling showed that the structure of the mutant protein was different with that wild-type Cx50.
The missense mutation c.139G > A in GJA8 gene is associated with autosomal dominant congenital cataract in a six-generation Chinese family. The result of this present study provides further evidence that the p. D47N mutation in CX50 is a hot-spot mutation.
先天性白内障是婴儿期或幼儿期失明的最常见原因。迄今为止,已鉴定出40多个与先天性白内障相关的基因座,包括不同染色体上至少26个与遗传性白内障相关的基因。本研究旨在鉴定一个患先天性白内障的六代中国家系中的基因突变。
记录了详细的六代中国白内障家系病史和家庭成员的临床资料。共招募了27名家庭成员,包括14名患者和13名未患病个体。进行全外显子组测序以确定致病突变。采用桑格测序法确认结果。
在Cx50中鉴定出一个已知的错义突变,即c.139G>A(p.D47N)。该突变与所有患病个体共分离,在未患病家庭成员或100名无关对照中未观察到。同源建模显示突变蛋白的结构与野生型Cx50不同。
GJA8基因中的错义突变c.139G>A与一个六代中国家系中的常染色体显性先天性白内障相关。本研究结果进一步证明CX50中的p.D47N突变是一个热点突变。