Jarayseh Tamara, Guillemyn Brecht, De Saffel Hanna, Bek Jan Willem, Syx Delfien, Symoens Sofie, Gansemans Yannick, Van Nieuwerburgh Filip, Jagadeesh Sujatha, Raja Jayarekha, Malfait Fransiska, Coucke Paul J, De Clercq Adelbert, Willaert Andy
Center for Medical Genetics Ghent, Department of Biomolecular Medicine, Ghent University, Ghent, Belgium.
Laboratory of Pharmaceutical Biotechnology, Faculty of Pharmaceutical Sciences, Ghent University, Ghent, Belgium.
Hum Genet. 2023 Mar;142(3):457-476. doi: 10.1007/s00439-022-02518-w. Epub 2023 Jan 25.
Bi-allelic mutations in the gene coding for human trans-membrane anterior-posterior transformation protein 1 (TAPT1) result in a broad phenotypic spectrum, ranging from syndromic disease with severe skeletal and congenital abnormalities to isolated early-onset cataract. We present here the first patient with a frameshift mutation in the TAPT1 gene, resulting in both bilateral early-onset cataract and skeletal abnormalities, in addition to several dysmorphic features, in this way further expanding the phenotypic spectrum associated with TAPT1 mutations. A tapt1a/tapt1b double knock-out (KO) zebrafish model generated by CRISPR/Cas9 gene editing revealed an early larval phenotype with eye malformations, loss of vision, increased photokinetics and hyperpigmentation, without visible skeletal involvement. Ultrastructural analysis of the eyes showed a smaller condensed lens, loss of integrity of the lens capsule with formation of a secondary lens and hyperplasia of the cells in the ganglion and inner plexiform layers of the retina. Transcriptomic analysis pointed to an impaired lens development with aberrant expression of many of the crystallin and other lens-specific genes. Furthermore, the phototransduction and visual perception pathways were found to be significantly disturbed. Differences in light perception are likely the cause of the increased dark photokinetics and generalized hyperpigmentation observed in this zebrafish model. In conclusion, this study validates TAPT1 as a new gene for early-onset cataract and sheds light on its ultrastructural and molecular characteristics.
编码人类跨膜前后转化蛋白1(TAPT1)的基因双等位基因突变会导致广泛的表型谱,范围从伴有严重骨骼和先天性异常的综合征性疾病到孤立的早发性白内障。我们在此报告首例TAPT1基因发生移码突变的患者,该患者除了有多种畸形特征外,还患有双侧早发性白内障和骨骼异常,从而进一步扩大了与TAPT1突变相关的表型谱。通过CRISPR/Cas9基因编辑产生的tapt1a/tapt1b双敲除(KO)斑马鱼模型显示出早期幼虫表型,伴有眼睛畸形、视力丧失、光动力学增加和色素沉着过多,但未见明显的骨骼受累。眼睛的超微结构分析显示晶状体较小且浓缩,晶状体囊完整性丧失,形成次生晶状体,视网膜神经节层和内网状层细胞增生。转录组分析表明晶状体发育受损,许多晶状体蛋白和其他晶状体特异性基因表达异常。此外,发现光转导和视觉感知通路受到明显干扰。光感知差异可能是该斑马鱼模型中观察到的暗光动力学增加和全身性色素沉着过多的原因。总之这项研究证实TAPT1是早发性白内障的一个新基因,并揭示了其超微结构和分子特征。