Faculty of Bioindustry, Tokyo University of Agriculture, 196 Yasaka, Abashiri, Hokkaido 099-2493, Japan.
Mammalian Genetics Project, Department of Genome Medicine, Tokyo Metropolitan Institute of Medical Science, 2-1-6 Kamikitazawa, Setagaya-ku, Tokyo 156-8506, Japan.
Exp Anim. 2019 Nov 6;68(4):397-406. doi: 10.1538/expanim.19-0020. Epub 2019 May 20.
Visual impairment leads to a decrease in quality of life. Cataract is the most commonly observed ocular disease in humans that causes vision disorders. The risk factors associated with cataract development include aging, infections, eye injuries, environmental causes, such as radiation and exposure to ultraviolet rays in sunlight, and genetic mutations. Additionally, several cataract patients display phenotypic heterogeneity, suggesting the role of genetic modifiers in the modulation of severity and onset time of cataractogenesis. However, the genetic modifiers associated with cataract have not been identified in humans yet. In contrast, the identification and mapping of genetic modifiers have been successfully carried out in mice and rats. In this review, we focus on the genetic modifiers of cataract in the rodent models.
视力障碍会导致生活质量下降。白内障是人类最常见的眼部疾病,可导致视力障碍。白内障发生的相关风险因素包括衰老、感染、眼部损伤、环境因素,如辐射和阳光中的紫外线暴露,以及基因突变。此外,一些白内障患者表现出表型异质性,表明遗传修饰因子在调节白内障发生的严重程度和发病时间方面发挥作用。然而,与白内障相关的遗传修饰因子尚未在人类中被鉴定。相比之下,在小鼠和大鼠中已经成功地进行了遗传修饰因子的鉴定和定位。在这篇综述中,我们专注于啮齿动物模型中的白内障遗传修饰因子。