{"title":"PLCZ1基因突变导致受精障碍1例。","authors":"Yuxing Xiong, Yan Liu, Mei Tang, Sha Shi, Yu Wang","doi":"10.5935/1518-0557.20250028","DOIUrl":null,"url":null,"abstract":"<p><strong>Objective: </strong>Sperm-specific phospholipase C-zeta (PLCζ) is a sperm-derived oocyte activating factor, which can induce Ca2+ oscillation and initiate oocyte activation. The mutation of this gene will affect oocyte activation and lead to fertilization failure(FF). In this paper, we report a fertilization disorder caused by a PLCZ1 gene mutation. The patient's peripheral blood was collected for whole exon detection. The results showed that the patient had heterozygous mutations in PLCZ1 gene c.1733 C > T (p.M578L) and c.471 G > C (p.M157I), and the male's brother also carried heterozygous mutations in the gene. Finally, the patient obtained clinical pregnancy by in vitro fertilization with donor sperm. At the same time, the related literature on PLCZ1 gene mutation at home and abroad was reviewed and analyzed to improve the clinicians' understanding of the PLCZ1 gene and fertilization disorders.</p>","PeriodicalId":520656,"journal":{"name":"JBRA assisted reproduction","volume":" ","pages":""},"PeriodicalIF":1.9000,"publicationDate":"2025-08-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"PLCZ1 gene mutation leads to fertilization disorder: a case report.\",\"authors\":\"Yuxing Xiong, Yan Liu, Mei Tang, Sha Shi, Yu Wang\",\"doi\":\"10.5935/1518-0557.20250028\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>Sperm-specific phospholipase C-zeta (PLCζ) is a sperm-derived oocyte activating factor, which can induce Ca2+ oscillation and initiate oocyte activation. The mutation of this gene will affect oocyte activation and lead to fertilization failure(FF). In this paper, we report a fertilization disorder caused by a PLCZ1 gene mutation. The patient's peripheral blood was collected for whole exon detection. The results showed that the patient had heterozygous mutations in PLCZ1 gene c.1733 C > T (p.M578L) and c.471 G > C (p.M157I), and the male's brother also carried heterozygous mutations in the gene. Finally, the patient obtained clinical pregnancy by in vitro fertilization with donor sperm. At the same time, the related literature on PLCZ1 gene mutation at home and abroad was reviewed and analyzed to improve the clinicians' understanding of the PLCZ1 gene and fertilization disorders.</p>\",\"PeriodicalId\":520656,\"journal\":{\"name\":\"JBRA assisted reproduction\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.9000,\"publicationDate\":\"2025-08-12\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"JBRA assisted reproduction\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5935/1518-0557.20250028\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"JBRA assisted reproduction","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5935/1518-0557.20250028","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
目的:精子特异性磷脂酶c - ζ (PLCζ)是精子源性卵母细胞活化因子,可诱导Ca2+振荡,启动卵母细胞活化。该基因的突变会影响卵母细胞的激活,导致受精失败(FF)。在本文中,我们报告了一个由PLCZ1基因突变引起的受精障碍。采集患者外周血进行全外显子检测。结果显示患者PLCZ1基因c.1733存在杂合突变C > T (p.M578L)和C 471G b> C (p.M157I),而男性的兄弟也携带该基因的杂合突变。最后,患者通过供体精子体外受精获得临床妊娠。同时,对国内外PLCZ1基因突变的相关文献进行综述和分析,以提高临床医生对PLCZ1基因与受精障碍的认识。
PLCZ1 gene mutation leads to fertilization disorder: a case report.
Objective: Sperm-specific phospholipase C-zeta (PLCζ) is a sperm-derived oocyte activating factor, which can induce Ca2+ oscillation and initiate oocyte activation. The mutation of this gene will affect oocyte activation and lead to fertilization failure(FF). In this paper, we report a fertilization disorder caused by a PLCZ1 gene mutation. The patient's peripheral blood was collected for whole exon detection. The results showed that the patient had heterozygous mutations in PLCZ1 gene c.1733 C > T (p.M578L) and c.471 G > C (p.M157I), and the male's brother also carried heterozygous mutations in the gene. Finally, the patient obtained clinical pregnancy by in vitro fertilization with donor sperm. At the same time, the related literature on PLCZ1 gene mutation at home and abroad was reviewed and analyzed to improve the clinicians' understanding of the PLCZ1 gene and fertilization disorders.