Department of Ophthalmology & Visual Sciences, UMass Medical School, Worcester, MA 01655, USA.
Division of Molecular Therapy, UCL Institute of Ophthalmology, London EC1V 9El, UK.
Hum Mol Genet. 2021 Jan 21;29(22):3706-3716. doi: 10.1093/hmg/ddaa269.
Mutations in retinitis pigmentosa GTPase regulator (RPGR) cause severe retinal ciliopathy, X-linked retinitis pigmentosa. Although two major alternatively spliced isoforms, RPGRex1-19 and RPGRORF15, are expressed, the relative importance of these isoforms in disease pathogenesis is unclear. Here, we analyzed fibroblast samples from eight patients and found that all of them form longer cilia than normal controls, albeit to different degrees. Although all mutant RPGRORF15 messenger RNAs (mRNAs) are unstable, their steady-state levels were similar or higher than those in the control cells, suggesting there may be increased transcription. Three of the fibroblasts that had higher levels of mutant RPGRORF15 mRNA also exhibited significantly higher levels of RPGRex1-19 mRNA. Four samples with unaltered RPGRex1-19 levels carried mutations in RPGRORF15 that resulted in this isoform being relatively less stable. Thus, in all cases, the RPGRex1-19/RPGRORF15 isoform ratio was increased, and this was highly correlative to the cilia extension defect. Moreover, overexpression of RPGRex1-19 (mimicking the increase in RPGRex1-19 to RPGRORF15 isoform ratio) or RPGRORF15 (mimicking reduction of the ratio) resulted in significantly longer or shorter cilia, respectively. Notably, the cilia length defect appears to be attributable to both the loss of the wild-type RPGRORF15 protein and to the higher levels of the RPGRex1-19 isoform, indicating that the observed defect is due to the altered isoform ratios. These results suggest that maintaining the optimal RPGRex1-9 to RPGRORF15 ratio is critical for cilia growth and that designing strategies that focus on the best ways to restore the RPGRex1-19/RPGRORF15 ratio may lead to better therapeutic outcomes.
RPGR 基因突变导致严重的视网膜纤毛病变,X 连锁视网膜色素变性。尽管表达了两种主要的选择性剪接异构体 RPGRex1-19 和 RPGRORF15,但这些异构体在疾病发病机制中的相对重要性尚不清楚。在这里,我们分析了来自 8 名患者的成纤维细胞样本,发现它们的纤毛都比正常对照长,尽管程度不同。虽然所有突变的 RPGRORF15 信使 RNA(mRNA)都不稳定,但它们的稳定水平与对照细胞相似或更高,这表明可能存在转录增加。三种具有更高水平的突变 RPGRORF15 mRNA 的成纤维细胞也表现出明显更高水平的 RPGRex1-19 mRNA。四个具有未改变的 RPGRex1-19 水平的样本携带 RPGRORF15 突变,导致该异构体相对不稳定。因此,在所有情况下,RPGRex1-19/RPGRORF15 异构体的比例增加,这与纤毛延伸缺陷高度相关。此外,过表达 RPGRex1-19(模拟 RPGRex1-19 与 RPGRORF15 异构体比例的增加)或 RPGRORF15(模拟比例的降低)分别导致纤毛显著变长或变短。值得注意的是,纤毛长度缺陷似乎归因于野生型 RPGRORF15 蛋白的丧失和 RPGRex1-19 异构体水平的升高,表明观察到的缺陷是由于改变的异构体比例。这些结果表明,维持最佳的 RPGRex1-9 与 RPGRORF15 比例对于纤毛生长至关重要,并且设计专注于最佳方式恢复 RPGRex1-19/RPGRORF15 比例的策略可能会导致更好的治疗结果。