Department of Medical Genetics, University of Alberta, Edmonton, AB T6G 2H7, Canada.
Division of Anatomy, Department of Surgery, University of Alberta, Edmonton, AB T6G 2H7, Canada.
Cells. 2020 Sep 30;9(10):2214. doi: 10.3390/cells9102214.
Photoreceptor disease results in irreparable vision loss and blindness, which has a dramatic impact on quality of life. Pathogenic mutations in lead to photoreceptor degenerations such as occult macular dystrophy and retinitis pigmentosa. RP1L1 is a component of the photoreceptor axoneme, the backbone structure of the photoreceptor's light-sensing outer segment. We generated an zebrafish mutant using CRISPR/Cas9 genome editing. Mutant animals had progressive photoreceptor functional defects as determined by electrophysiological assessment. Optical coherence tomography showed gaps in the photoreceptor layer, disrupted photoreceptor mosaics, and thinner retinas. Mutant retinas had disorganized photoreceptor outer segments and lipid-rich subretinal drusenoid deposits between the photoreceptors and retinal pigment epithelium. Our mutant is a novel model of -associated photoreceptor disease and the first zebrafish model of photoreceptor degeneration with reported subretinal drusenoid deposits, a feature of age-related macular degeneration.
光感受器疾病导致不可逆转的视力丧失和失明,严重影响生活质量。导致光感受器变性的致病性突变,如隐匿性黄斑营养不良和色素性视网膜炎。RP1L1 是光感受器轴丝的一个组成部分,光感受器的感光外节的骨干结构。我们使用 CRISPR/Cas9 基因组编辑生成了一种 斑马鱼突变体。通过电生理评估确定,突变动物的光感受器功能逐渐出现缺陷。光学相干断层扫描显示光感受器层有空隙,光感受器马赛克紊乱,视网膜变薄。突变体视网膜的光感受器外节排列紊乱,光感受器和视网膜色素上皮之间有富含脂质的视网膜下 drusenoid 沉积物。我们的突变体是一种新型的 相关光感受器疾病模型,也是第一个报道有视网膜下 drusenoid 沉积物的光感受器变性的斑马鱼模型,这是年龄相关性黄斑变性的一个特征。