在FAM71D的有害变异导致男性不孕症与asthenoteratospermia
Xiaobin Zhu1, Liu Liu2,3, Shixiong Tian4
1Department of Gynecology and Obstetrics, Reproductive Medical Center, Shanghai Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200025, China.
Molecular genetics and genomics : MGG
|March 15, 2024
概括
一种新的基因突变,FAM71D,被确定为导致男性不孕症的原因. 这一发现为受影响个体提供了新的遗传见解和潜在的辅助生殖策略.
科学领域:
- 遗传学 是一个遗传学.
- 生殖生物学 生殖生物学
- 人类分子遗传学
背景情况:
- 阿斯诺特精症显著导致男性不孕症.
- 仅在丸中发现的FAM71D蛋白与精子运动有关.
- 在男性不孕症中FAM71D突变的作用仍然未被探索.
研究的目的:
- 调查FAM71D突变与男性不孕症之间的关联.
- 为了识别FAM71D中负责阿斯诺特精症的遗传变异.
主要方法:
- 在来自血缘亲属家庭的不孕男性身上进行了全外测序.
- 生物信息学工具预测了已识别的FAM71D变种的致病性.
- 进行了精液分析和免疫光试验.
主要成果:
- 在受影响的个体中,在FAM71D中发现了一种同卵性误解突变 (c.440G>A,p.Arg147Gln).
- 这种FAM71D变种很罕见,预计会有害.
- 精液分析显示精子运动性下降和形态缺陷.
- 突变影响了精子结构蛋白的组装.
结论:
- FAM71D被确定为一种新型的男性不孕症致病基因,呈现为阿斯诺特精症.
- 内细胞质精子注射 (ICSI) 对患者产生了积极的结果.
- 这些发现为在阿斯诺特精症病例中进行遗传咨询和辅助生殖提供了指导.
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