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Novel CCDC188 variants cause acephalic spermatozoa syndrome with poor intracytoplasmic sperm injection outcome.

作者信息

Yang Xiaoyu, Wang Yu, Yu Kexin, Xiang Mingfei, Zhang Jingjing, Duan Zongliu, Zhou Yiru, Zha Xiaomin, Li Honglin, Wang Fengsong, Cao Yunxia, Zhu Fuxi

机构信息

State Key Laboratory of Reproductive Medicine and Offspring Health, Clinical Center of Reproductive Medicine, the First Affiliated Hospital of Nanjing Medical University, Nanjing, 210029, Jiangsu, China.

Reproductive Medicine Center, Department of Obstetrics and Gynecology, the Second Affiliated Hospital of Anhui Medical University, Hefei, 230601, Anhui, China.

出版信息

J Assist Reprod Genet. 2025 Sep 26. doi: 10.1007/s10815-025-03659-3.

DOI:10.1007/s10815-025-03659-3
PMID:41004021
Abstract

PURPOSE

To identify novel CCDC188 variants in acephalic spermatozoa syndrome (ASS) patients and investigated the potential effect on the outcome of intracytoplasmic sperm injection (ICSI).

METHODS

Sixteen patients diagnosed as ASS by morphological analysis were recruited in the first half of 2023. Whole exome sequencing (WES) and Sanger sequencing were performed to identify the genetic cause and define the hereditary mode, using genomic DNA extracted from peripheral blood. Morphological characteristics of sperm were revealed by hematoxylin and eosin (H&E) staining and transmission electron microscopy (TEM). Pathogenicity of variants was evaluated in silico, and further confirmed in vitro and vivo by western blotting (WB), reverse transcript-polymerase chain reaction (RT-PCR), quantitative real-time PCR (qPCR), and immunofluorescence (IF). ICSI was performed with a standard operation procedure as the treatment strategy.

RESULTS

Two novel variants in CCDC188 (NM_001365892.2: c.481C > T[p.Gln161*] and c.1022 + 1G > A[p. K325Afs*110]) were identified in two unrelated infertile men. Morphological analysis displayed the typical ASS phenotype of patients' sperm. The depletion of CCDC188 protein was observed accompanied with SUN5 and PMFBP1 in patients' sperm. Notably, a poor ICSI outcome occurred after a sperm head and a detached tail from one patient were simultaneously microinjected, caused by fertilization failure and abnormal embryo development.

CONCLUSIONS

Our results broadened the variant spectrum of CCDC188. We firstly reported a poor outcome of one proband after ICSI treatment, which suggested the role played by CCDC188 in male infertility might involve not only spermatogenesis but also fertilization and early embryonic development.

摘要

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本文引用的文献

1
Loss of CCDC188 causes male infertility with defects in the sperm head-neck connection in mice†.CCDC188缺失导致小鼠雄性不育,并伴有精子头部与颈部连接缺陷† 。
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Discovery of CCDC188 gene as a novel genetic target for human acephalic spermatozoa syndrome.CCDC188基因作为人类无头精子症新遗传靶点的发现。
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Identification of CFAP52 as a novel diagnostic target of male infertility with defects of sperm head-tail connection and flagella development.
鉴定 CFAP52 为一种新型的精子头-尾连接和鞭毛发育缺陷导致的男性不育症的诊断靶点。
Elife. 2023 Dec 21;12:RP92769. doi: 10.7554/eLife.92769.
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Identification of nonfunctional SPATA20 causing acephalic spermatozoa syndrome in humans.鉴定导致无头精子症的非功能性 SPATA20 基因。
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Biallelic mutations in spermatogenesis and centriole-associated 1 like () cause acephalic spermatozoa syndrome and male infertility.生精和中心体相关蛋白 1 样基因()的双等位基因突变导致无头精子症和男性不育。
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