Department of Andrology, Women and Children's Hospital, School of Medicine, Xiamen University, Xiamen, Fujian, China.
Fujian Provincial Key Laboratory of Reproductive Health Research, School of Medicine, Xiamen University, Xiamen, Fujian, China.
Andrology. 2023 Sep;11(6):1121-1131. doi: 10.1111/andr.13407. Epub 2023 Feb 23.
Oligoasthenoteratozoospermia (OAT) is one of the most complex aggregators of male gametic problems. However, the genetic etiology of OAT is still largely unknown.
To reveal the new genetic factors responsible for male infertility owning to OAT and reveal the outcomes of the affected patients from intracytoplasmic sperm injection (ICSI).
Two infertile men with typical OAT were recruited in 2018 and retrospected a cohort that included 47 patients with OAT from 2013 to 2021. Fifty healthy men with proven fertility served as control subjects. To identify the novel pathogenic variants, whole-exome sequencing and Sanger sequencing were used. In silico analysis revealed the affecting of the variants. Field emission scanning electron microscopy was employed to observe the morphological defects of the spermatozoa. Immunofluorescence was used to analyze the expression and localization of the related protein. CRISPR/Cas9 was used to generate the mouse model. ICSI was used as a treatment for the patients and to assess the effects of the pathogenic variant on fertilization and embryo development.
We identified a loss-of-function mutation NM_001170574.2:c.823G > T (p.Glu275*) in X-linked TENT5D from two patients with OAT. This variant is highly deleterious and has not been found in the human population. The count of patients' spermatozoa is dramatically decreased and displays multiple morphologic abnormalities with poor motility. Tent5d knockout mice are infertile and exhibit parallel defects. ICSI could rescue the infertility of the Tent5d knockout male mice. Moreover, the proband was treated with ICSI and achieved a successful pregnancy outcome for the first time. Subsequent mutation screening identified no TENT5D mutations among 47 additional patients with OAT and 50 control subjects.
Mutation in TENT5D results in OAT and male infertility, and this terrible situation could be rescued by ICSI.
少弱畸形精子症(OAT)是男性配子问题最复杂的聚集因素之一。然而,OAT 的遗传病因在很大程度上仍不清楚。
揭示导致男性不育的 OAT 的新遗传因素,并揭示接受胞浆内单精子注射(ICSI)治疗的患者的结果。
2018 年招募了 2 名患有典型 OAT 的不育男性,并回顾性分析了 2013 年至 2021 年期间的 47 名 OAT 患者的队列。50 名生育能力正常的健康男性作为对照。使用全外显子组测序和 Sanger 测序来鉴定新的致病性变异。进行了计算机分析以揭示变异的影响。使用场发射扫描电子显微镜观察精子的形态缺陷。使用免疫荧光分析相关蛋白的表达和定位。使用 CRISPR/Cas9 生成了小鼠模型。ICSI 用于治疗患者,并评估致病性变异对受精和胚胎发育的影响。
我们在 2 名 OAT 患者中发现了 X 连锁 TENT5D 中的无功能突变 NM_001170574.2:c.823G>T(p.Glu275*)。该变体高度有害,在人群中未发现。患者精子的数量明显减少,并显示出多种形态异常,运动能力差。Tent5d 敲除小鼠不育,表现出平行缺陷。ICSI 可以挽救 Tent5d 敲除雄性小鼠的不育症。此外,该先证者接受 ICSI 治疗,首次成功妊娠。随后的突变筛查在另外 47 名 OAT 患者和 50 名对照中均未发现 TENT5D 突变。
TENT5D 的突变导致 OAT 和男性不育,这种严重情况可以通过 ICSI 来挽救。