PHYH c.678+5G>T 导致框架内外显子跳过,并与减弱的 Refsum 疾病相关
Malena Daich Varela1,2, Elena Schiff1, Samantha Malka1
1Moorfields Eye Hospital, London, United Kingdom.
Investigative ophthalmology & visual science
|February 27, 2024
概括
这种PHYH:c.678+5G>T变体显著影响PHYH基因拼接,导致视网膜色素炎. 这一发现支持将变种归类为致病性,并建议对受影响个体进行植物酸测试.
科学领域:
- 遗传学 遗传学 是一个
- 分子生物学分子生物学
- 眼科医生 眼科 眼科
背景情况:
- 在ClinVar.中,PHYH:c.678+5G>T变体有相互矛盾的解释.
- 这种变体在南亚人口中最大的等位基因频率为0.0045,在gnomAD.
- 皮质视网膜炎 (retinitis pigmentosa) 是一组遗传性眼睛疾病.
研究的目的:
- 为了研究PHYH:c.678+5G>T变体的分子效应.
- 为了确定PHYH:c.678+5G>T变异的致病性.
主要方法:
- 招募了患有视网膜色素炎和双的PHYH变体的患者.
- 从血液样本中净化总RNA.
- 进行PCR放大,牛津纳米孔测序和片测序.
主要成果:
- 分析了四名患有视网膜色素炎和轻微眼外发现的患者.
- 植物酸的含量从正常到明显高不等.
- 在内突变突变突变跳转 (第5和第6个突变突变突变) 在31.1%至88.4%的amplicon中被观察到.
- 较小比例的安普利康只跳过了6号外子 (0%至11.3%).
结论:
- 这种PHYH:c.678+5G>T变体显著影响PHYH转录拼接.
- 拼接缺陷的框架内性质与轻度的临床表现相关.
- 这些发现支持将该变种归类为致病性.
- 双性PHYH变异患者应接受植物酸检测.
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