Yuan Lin, Sui Tingting, Chen Mao, Deng Jichao, Huang Yongye, Zeng Jian, Lv Qingyan, Song Yuning, Li Zhanjun, Lai Liangxue
Jilin Provincial Key Laboratory of Animal Embryo Engineering, College of Animal Sciences, Jilin University, Changchun, 130062, China.
College of Life and Health Sciences, Northeastern University, Shen Yang, China.
Sci Rep. 2016 Feb 25;6:22024. doi: 10.1038/srep22024.
Cataracts are the leading cause of vision loss in the world, although surgical treatment can restore vision in cataract patients. Until now, there have been no adequate animal models for in vivo studies of artificial lens safety and drug interactions. Genetic studies have demonstrated that GJA8 is involved in maintaining lens opacity and proper lens development. In this study, a cataract model with GJA8 gene knockout was developed via co-injection of Cas9/sgRNA mRNA into rabbit zygotes. Our results showed that gene mutation efficiency in the GJA8 locus reached 98.7% in embryos and 100% in pups, demonstrating that the Cas9/sgRNA system is a highly efficient tool for gene editing in rabbits. In agreement with other studies, our genetic and histology results showed that impaired GJA8 function caused microphthalmia, small lens size and cataracts. In summary, our novel rabbit model of cataracts will be an important drug-screening tool for cataract prevention and treatment.
白内障是全球视力丧失的主要原因,尽管手术治疗可以恢复白内障患者的视力。到目前为止,还没有合适的动物模型用于人工晶状体安全性和药物相互作用的体内研究。基因研究表明,GJA8参与维持晶状体混浊和晶状体的正常发育。在本研究中,通过将Cas9/sgRNA mRNA共注射到兔受精卵中,建立了GJA8基因敲除的白内障模型。我们的结果表明,GJA8基因座的基因突变效率在胚胎中达到98.7%,在幼崽中达到100%,表明Cas9/sgRNA系统是兔基因编辑的高效工具。与其他研究一致,我们的基因和组织学结果表明,GJA8功能受损会导致小眼症、晶状体尺寸变小和白内障。总之,我们新型的兔白内障模型将成为白内障防治重要的药物筛选工具。