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导致顶体脱离、精子头部畸形和男性生育力低下/不育症。

Disruption in leads to acrosome detachment, sperm head deformity, and male in/subfertility in humans and mice.

机构信息

Key Laboratory of Cell Proliferation and Regulation Biology, Ministry of Education, Department of Biology, College of Life Sciences, Beijing Normal University, Beijing, China.

Department of Assisted Reproduction, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

出版信息

Elife. 2024 Apr 4;13:RP95054. doi: 10.7554/eLife.95054.

DOI:10.7554/eLife.95054
PMID:38573307
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10994659/
Abstract

The perinuclear theca (PT) is a dense cytoplasmic web encapsulating the sperm nucleus. The physiological roles of PT in sperm biology and the clinical relevance of variants of PT proteins to male infertility are still largely unknown. We reveal that cylicin-1, a major constituent of the PT, is vital for male fertility in both mice and humans. Loss of cylicin-1 in mice leads to a high incidence of malformed sperm heads with acrosome detachment from the nucleus. Cylicin-1 interacts with itself, several other PT proteins, the inner acrosomal membrane (IAM) protein SPACA1, and the nuclear envelope (NE) protein FAM209 to form an 'IAM-cylicins-NE' sandwich structure, anchoring the acrosome to the nucleus. WES (whole exome sequencing) of more than 500 Chinese infertile men with sperm head deformities was performed and a variant was identified in 19 patients. -mutant mice carrying this variant also exhibited sperm acrosome/head deformities and reduced fertility, indicating that this variant most likely affects human male reproduction. Furthermore, the outcomes of assisted reproduction were reported for patients harbouring the variant. Our findings demonstrate a critical role of cylicin-1 in the sperm acrosome-nucleus connection and suggest variants as potential risk factors for human male fertility.

摘要

核周质(PT)是包裹精子核的密集细胞质网络。PT 在精子生物学中的生理作用以及 PT 蛋白变体与男性不育的临床相关性在很大程度上仍然未知。我们揭示了 cyclin-1 是 PT 的主要成分之一,对于小鼠和人类的雄性生育力都是至关重要的。cyclin-1 在小鼠中的缺失会导致畸形精子头的发生率很高,其顶体与核脱离。cyclin-1 与自身、其他几种 PT 蛋白、顶体内部膜(IAM)蛋白 SPACA1 和核膜(NE)蛋白 FAM209 相互作用,形成“IAM-cyclin-NE”三明治结构,将顶体锚定在核上。对 500 多名患有精子头畸形的中国不育男性进行了 WES(全外显子组测序),在 19 名患者中发现了一个 变体。携带该变体的 -mutant 小鼠也表现出顶体/头部畸形和生育能力下降,表明该变体很可能影响人类男性生殖。此外,还报告了携带该变体的患者的辅助生殖结果。我们的研究结果表明 cyclin-1 在精子顶体-核连接中起着关键作用,并表明变体可能是人类男性生育力的潜在风险因素。

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本文引用的文献

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Cylicins are a structural component of the sperm calyx being indispensable for male fertility in mice and human. cyclin 是精子花萼的结构组成部分,对于小鼠和人类的雄性生育能力是不可或缺的。
Elife. 2023 Nov 28;12:RP86100. doi: 10.7554/eLife.86100.
2
Mutations in CCIN cause teratozoospermia and male infertility.CCIN基因的突变会导致畸形精子症和男性不育。
Sci Bull (Beijing). 2022 Oct 31;67(20):2112-2123. doi: 10.1016/j.scib.2022.09.026. Epub 2022 Sep 26.
3
The perinuclear theca protein Calicin helps shape the sperm head and maintain the nuclear structure in mice.
核周质蛋白 Calicin 有助于塑造精子头部并维持小鼠的核结构。
Cell Rep. 2022 Jul 5;40(1):111049. doi: 10.1016/j.celrep.2022.111049.
4
Loss of perinuclear theca ACTRT1 causes acrosome detachment and severe male subfertility in mice.核周质 ACTRT1 的缺失导致小鼠顶体脱离和严重的雄性不育。
Development. 2022 Jun 15;149(12). doi: 10.1242/dev.200489. Epub 2022 Jun 21.
5
Interpretation and reporting of large regions of homozygosity and suspected consanguinity/uniparental disomy, 2021 revision: A technical standard of the American College of Medical Genetics and Genomics (ACMG).大片段同源性和疑似亲缘关系/单亲二倍体性的解读和报告,2021 年修订版:美国医学遗传学与基因组学学会(ACMG)的技术标准。
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6
Variant interpretation using population databases: Lessons from gnomAD.使用人群数据库进行变异解释:来自 gnomAD 的经验。
Hum Mutat. 2022 Aug;43(8):1012-1030. doi: 10.1002/humu.24309. Epub 2021 Dec 16.
7
FAM209 associates with DPY19L2, and is required for sperm acrosome biogenesis and fertility in mice.FAM209 与 DPY19L2 相关,对于精子顶体生物发生和小鼠的生育能力是必需的。
J Cell Sci. 2021 Nov 1;134(21). doi: 10.1242/jcs.259206.
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Loss of SPACA1 function causes autosomal recessive globozoospermia by damaging the acrosome-acroplaxome complex.SPACA1 功能丧失通过破坏顶体-赤道板复合物导致常染色体隐性遗传的圆头精子症。
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Homozygous pathogenic variants in ACTL9 cause fertilization failure and male infertility in humans and mice.ACTL9 中的纯合致病性变异可导致人类和小鼠的受精失败和男性不育。
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Disruption in causes acrosomal ultrastructural defects in human and mouse sperm as a novel male factor inducing early embryonic arrest.[此处英文原文不完整,缺少具体所指的“Disruption in”后面的内容]导致人类和小鼠精子顶体超微结构缺陷,这是一种导致早期胚胎停滞的新型男性因素。
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