Cui Xiu-Kun, Zhu Ke-Ke, Zhou Zheng, Wan Si-Min, Dong Yi, Wang Xuan-Ce, Li Jing, Zhang Jing, Mu Hong-Mei, Qin Lei, Hu Yan-Zhong
Henan International Union Laboratory of Antibody Medicine, Department of Cell biology and Genetics, Henan University School of Medicine, Kaifeng 475004, Henan Province, China.
Kaifeng Key Lab of Cataract and Myopia, Institute of Eye Diseases, Kaifeng Centre Hospital, Kaifeng 475000, Henan Province, China.
Int J Ophthalmol. 2017 May 18;10(5):684-690. doi: 10.18240/ijo.2017.05.04. eCollection 2017.
To investigate the genetic mutations that are associated the hereditary autosomal dominant cataract in a Chinese family.
A Chinese family consisting of 20 cataract patients (including 9 male and 11 female) and 2 unaffected individuals from 5 generations were diagnosed to be a typical autosomal dominant cataract pedigree. Genomic DNA samples were extracted from the peripheral blood cells of the participants in this pedigree. Exon sequence was used for genetic mutation screening. In silico analysis was used to study the structure characteristics of connexin 46 (CX46) mutant. Immunoblotting was conduceted for testing the expression of CX46.
To determine the involved genetic mutations, 11 well-known cataract-associated genes (cryaa, cryab, crybb1, crybb2, crygc, crygd, Gja3, Gja8, Hsf4, Mip and Pitx3) were chosen for genetic mutation test by using exon sequencing. A novel cytosine insertion at position 1195 of CX46 cDNA (c.1194_1195ins C) was found in the samples of 5 tested cataract patients but not in the unaffected 2 individuals nor in normal controls, which resulted in 30 amino acids more extension in CX46C-terminus (cx46fs400) compared with the wild-type CX46. In silico protein structure analysis indicated that the mutant showed distinctive hydrophobicity and protein secondary structure compared with the wild-type CX46. The immunoblot results revealed that CX46 protein, which expressed in the aging cataract lens tissues, was absence in the proband lens. In contrast, CX50, alpha A-crystallin and alphaB-crystallin expressed equally in both proband and aging cataract tissues. Those results revealed that the cx46fs400 mutation could impair CX46 protein expression.
The insertion of cytosine at position 1195 of CX46 cDNA is a novel mutation site that is associated with the autosomal dominant cataracts in this Chinese family. The C-terminal frameshift mutation is involved in regulating CX46 protein expression.
研究与一个中国家系遗传性常染色体显性白内障相关的基因突变。
一个由来自五代的20名白内障患者(包括9名男性和11名女性)以及2名未患病个体组成的中国家系被诊断为典型的常染色体显性白内障家系。从该家系参与者的外周血细胞中提取基因组DNA样本。采用外显子序列进行基因突变筛查。利用计算机分析研究连接蛋白46(CX46)突变体的结构特征。进行免疫印迹检测CX46的表达。
为确定相关基因突变,选择11个著名的白内障相关基因(cryaa、cryab、crybb1、crybb2、crygc、crygd、Gja3、Gja8、Hsf4、Mip和Pitx3),通过外显子测序进行基因突变检测。在5名受试白内障患者的样本中发现CX46 cDNA第1195位有一个新的胞嘧啶插入(c.1194_1195ins C),而在2名未患病个体及正常对照中未发现,这导致CX46 C末端比野生型CX46多延伸30个氨基酸(cx46fs400)。计算机蛋白质结构分析表明,与野生型CX46相比,该突变体具有独特的疏水性和蛋白质二级结构。免疫印迹结果显示,在衰老白内障晶状体组织中表达的CX46蛋白在先证者晶状体中缺失。相反,CX50、αA-晶体蛋白和αB-晶体蛋白在先证者和衰老白内障组织中的表达相同。这些结果表明cx46fs400突变可能损害CX46蛋白的表达。
CX46 cDNA第1195位胞嘧啶插入是该中国家系中与常染色体显性白内障相关的一个新突变位点。C末端移码突变参与调节CX46蛋白的表达。