Novel PLCZ1 mutation caused polyspermy during in vitro fertilization.

Asian journal of andrology Pub Date : 2024-07-01 Epub Date: 2024-03-05 DOI:10.4103/aja202376
Ke-Ya Tong, Wei-Wei Liu, Li-Wei Sun, Dong-Yun Liu, Ye-Zhou Xiang, Chong Li, Lu-Wei Chai, Ke Chen, Guo-Ning Huang, Jing-Yu Li
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Abstract

Failure of oocyte activation, including polyspermy and defects in pronuclear (PN) formation, triggers early embryonic developmental arrest. Many studies have shown that phospholipase C zeta 1 ( PLCZ1 ) mutations cause failure of PN formation following intracytoplasmic sperm injection (ICSI); however, whether PLCZ1 mutation is associated with polyspermy during in vitro fertilization (IVF) remains unknown. Whole-exome sequencing (WES) was performed to identify candidate mutations in couples with primary infertility. Sanger sequencing was used to validate the mutations. Multiple PLCZ1 -mutated sperm were injected into human and mouse oocytes to explore whether PN formation was induced. Assisted oocyte activation (AOA) after ICSI was performed to overcome the failure of oocyte activation. We identified three PLCZ1 mutations in three patients who experienced polyspermy during IVF cycles, including a novel missense mutation c.1154C>T, p.R385Q. PN formation failure was observed during the ICSI cycle. However, injection of multiple PLCZ1- mutated sperm induced PN formation, suggesting that the Ca 2+ oscillations induced by the sperm exceeded the necessary threshold for PN formation. AOA after ICSI enabled normal fertilization, and all patients achieved successful pregnancies. These findings expand the mutational spectrum of PLCZ1 and suggest an important role for PLCZ1 in terms of blocking polyspermy. Furthermore, this study may benefit genetic diagnoses in cases of abnormal fertilization and provide potential appropriate therapeutic measures for these patients with sperm-derived polyspermy.

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新型 PLCZ1 基因突变导致体外受精过程中的多精症。
摘要:卵母细胞活化失败,包括多核和原核(PN)形成缺陷,会引发早期胚胎发育停滞。许多研究表明,磷脂酶C zeta 1(PLCZ1)突变会导致卵胞浆内精子注射(ICSI)后原核形成失败;然而,PLCZ1突变是否与体外受精(IVF)过程中的多精症有关仍是未知数。研究人员在原发性不孕症夫妇中进行了全外显子组测序(WES),以确定候选突变。桑格测序用于验证突变。将多个 PLCZ1 基因突变的精子注入人类和小鼠卵母细胞,以探索是否会诱导 PN 的形成。在卵胞浆内单精子显微注射(ICSI)后进行辅助卵母细胞活化(AOA),以克服卵母细胞活化失败的问题。我们在试管婴儿周期中出现多胎妊娠的三名患者中发现了三个 PLCZ1 突变,其中包括一个新的错义突变 c.1154C>T,p.R385Q。在 ICSI 周期中观察到 PN 形成失败。然而,注射多个PLCZ1突变精子可诱导PN形成,这表明精子诱导的Ca2+振荡超过了PN形成的必要阈值。ICSI 后的 AOA 使受精正常,所有患者都成功怀孕。这些发现扩大了 PLCZ1 的突变范围,并表明 PLCZ1 在阻断多精子症方面发挥着重要作用。此外,这项研究可能有利于受精异常病例的基因诊断,并为这些精子衍生多精子症患者提供潜在的适当治疗措施。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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