在PABPC1L的新型变异导致女性因卵细胞成熟缺陷的不孕症
Zhiqi Pan1, Zhiqi Ye1, Hongjuan Ye2
1Institute of Pediatrics, Children's Hospital of Fudan University, the Institutes of Biomedical Sciences, and the State Key Laboratory of Genetic Engineering, Fudan University, Shanghai, China.
Journal of assisted reproduction and genetics
|November 23, 2025
概括
我们在PABPC1L基因中发现了五种新的致病变体,与卵细胞成熟缺陷和女性不孕症有关. 这些发现扩大了对不孕不育的遗传理解和诊断.
科学领域:
- 遗传学 遗传学 是一个
- 生殖生物学 生殖生物学
- 分子生物学分子生物学
背景情况:
- 卵细胞成熟缺陷是女性不孕症和反复出现的体外受精失败的重要原因.
- 确定这些缺陷的遗传基础对于准确的诊断和潜在的治疗策略至关重要.
研究的目的:
- 识别负责卵细胞成熟缺陷的基因中的新型致病变体.
- 为了研究这些变异对PABPC1L蛋白的功能影响.
主要方法:
- 在442名女性不孕症患者身上进行了全外组测序.
- 在分析和体外功能研究 (西式涂抹,免疫光,分子建模,循环胺追逐试验) 用于验证变异的致病性.
- 对两个独立的不育家庭的分析.
主要成果:
- 在两个家族中发现了五种新的PABPC1L变异 (四种错误,一种无意义),这些变异是由于自身遗传的.
- 这些变异导致PABPC1L蛋白降低调节,改变细胞质局部 (无意义变异),以及蛋白质稳定性受损 (错误变异).
结论:
- 这项研究扩大了PABPC1L已知的突变谱,证实了它在女性生殖中的重要作用.
- 这些发现支持女性不孕症的遗传诊断,并强调PABPC1L是卵细胞成熟的关键基因.
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