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本文引用的文献

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Am J Transl Res. 2025 Mar 15;17(3):1824-1833. doi: 10.62347/JFJX7128. eCollection 2025.
2
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Am J Transl Res. 2025 Mar 15;17(3):1780-1791. doi: 10.62347/VIVI6495. eCollection 2025.
3
NAE1-mediated neddylation coordinates ubiquitination regulation of meiotic recombination during spermatogenesis.NAE1介导的NEDDylation在精子发生过程中协调减数分裂重组的泛素化调控。
Theranostics. 2025 Feb 10;15(7):3122-3142. doi: 10.7150/thno.107843. eCollection 2025.
4
ASB1 engages with ELOB to facilitate SQOR ubiquitination and HS homeostasis during spermiogenesis.在精子发生过程中,ASB1与ELOB相互作用,以促进SQOR泛素化和血红素加氧酶系统稳态。
Redox Biol. 2025 Feb;79:103484. doi: 10.1016/j.redox.2024.103484. Epub 2024 Dec 27.
5
Discovery of small molecule inhibitors of neddylation catalyzing enzymes for anticancer therapy.发现用于癌症治疗的小分子量 neddylation 催化酶抑制剂。
Biomed Pharmacother. 2024 Oct;179:117356. doi: 10.1016/j.biopha.2024.117356. Epub 2024 Aug 29.
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Diversity of structure and function in Cullin E3 ligases.Cullin E3 连接酶的结构与功能多样性。
Curr Opin Struct Biol. 2024 Oct;88:102879. doi: 10.1016/j.sbi.2024.102879. Epub 2024 Jul 15.
7
DCUN1D1 and neddylation: Potential targets for cancer therapy.DCUN1D1 和 neddylation:癌症治疗的潜在靶点。
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8
E3 ligase FBXO22 is not significant for spermatogenesis and male fertility in mice.E3 泛素连接酶 FBXO22 对小鼠精子发生和雄性生育力并不重要。
Am J Transl Res. 2024 May 15;16(5):1834-1844. doi: 10.62347/STDA4237. eCollection 2024.
9
Ubiquitin-like modification dependent proteasomal degradation and disease therapy.泛素样修饰依赖的蛋白酶体降解与疾病治疗。
Trends Mol Med. 2024 Nov;30(11):1061-1075. doi: 10.1016/j.molmed.2024.05.005. Epub 2024 Jun 8.
10
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Ecotoxicol Environ Saf. 2024 Jul 1;279:116502. doi: 10.1016/j.ecoenv.2024.116502. Epub 2024 May 23.

DCUN1D2对小鼠精子发生和雄性生育力无显著影响。

DCUN1D2 is insignificant for spermatogenesis and male fertility in mice.

作者信息

Feng Yuxuan, Bao Mingyuan, Sheng Wenyi, Liu Shiqi, Cui Yuchen, Zhou Nianchao, Wu Tiantian, Huang Xiaoyan, Hou Shunyu, Liu Meng

机构信息

State Key Laboratory of Reproductive Medicine and Offspring Health, Department of Histology and Embryology, School of Basic Medical Sciences, Nanjing Medical University Nanjing 211166, Jiangsu, China.

Department of Thyroid and Breast Surgery, The Affiliated Suzhou Hospital of Nanjing Medical University, Suzhou Municipal Hospital, Gusu School, Nanjing Medical University Suzhou 215002, Jiangsu, China.

出版信息

Am J Transl Res. 2025 Jul 25;17(7):5614-5624. doi: 10.62347/CLIG5523. eCollection 2025.

DOI:10.62347/CLIG5523
PMID:40821035
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12351559/
Abstract

OBJECTIVES

Defective in cullin neddylation 1 domain containing 2 (DCUN1D2) belongs to the DCNLs family and can induce cell growth arrest and is also related to neddylation. While its potential role in spermatogenesis is hypothesized, the functional significance of DCUN1D2 in male germ cells remains undefined.

METHODS

To investigate this, germ cell and Sertoli cell-specific -knockouts were generated. Sperm parameters were analyzed via computer-assisted sperm analysis (CASA), while histological and immunofluorescence staining were employed to evaluate spermatogenic progression and apoptosis.

RESULTS

Compared with the control group, conditional knockout (cKO) mice exhibited no significant differences in histology, semen quality, sperm apoptosis or fertility tests.

CONCLUSIONS

This study indicated that DCUN1D2 has no significant effect on mouse spermatogenesis or male fertility. These findings will help avoid redundant studies and provide new information for the study of human fertility genes.

摘要

目的

含cullin泛素化激活酶1结构域蛋白2(DCUN1D2)属于DCNLs家族,可诱导细胞生长停滞,且与泛素化有关。虽然推测其在精子发生过程中具有潜在作用,但DCUN1D2在雄性生殖细胞中的功能意义仍不明确。

方法

为研究此问题,构建了生殖细胞和支持细胞特异性敲除小鼠。通过计算机辅助精子分析(CASA)分析精子参数,同时采用组织学和免疫荧光染色评估精子发生进程和细胞凋亡情况。

结果

与对照组相比,条件性敲除(cKO)小鼠在组织学、精液质量、精子凋亡或生育力测试方面均无显著差异。

结论

本研究表明,DCUN1D2对小鼠精子发生或雄性生育力无显著影响。这些发现将有助于避免冗余研究,并为人类生育基因的研究提供新信息。