[NSD1 regulates H3K36me2 in the pathogenesis of non-obstructive azoospermia].

Q4 Medicine
中华男科学杂志 Pub Date : 2025-03-01
Xuan Zhuang, Zhen-Xin Cai, Yu-Feng Yang, Zhi-Ming Li
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引用次数: 0

Abstract

Objective: To explore the role of nuclear receptor-binding SET-domain protein 1 (NSD1) in the pathogenesis of nonobstructive azoospermia (NOA) by regulating the expressions of relevant genes.

Methods: We detected the expression of NSD1 in the testis tissue of 7 male patients with obstructive azoospermia (OA) and 18 with NOA by qPCR and immunofluorescence assay, and determined the modification level of H3K36me2 in the testes of two groups of patients by immunofluorescence staining, Western blot and immunoprecipitation (IP). We examined the difference in the enrichment of H3K36me2 in the testis tissue by chromatin IP-based sequencing (ChIP-Seq), analyzed the genomic distribution and target genes using bioinformatics, and verified the expression levels of the target genes in the testes of the two groups of patients by qPCR.

Results: Compared with the patients with OA, those with NOA showed dramatically decreased mRNA and protein expressions of NSD1 (P=0.000 8). The binding of NSD1 to H3K36me2 was observed in the testis tissue of both the two groups of patients, while the modification level of H3K36me2 was evidently reduced in the NOA males. H3K36me2 was distributed mainly in the intergenic region in the testes of the two groups of patients, but the enrichment of H3K36me2 was obviously decreased in the NOA group. The differentially H3K36me2-enriched genes were involved in various biological processes, including tissue development, and cell morphogenesis. Results of ChIP-Seq and qPCR showed significantly down-regulated expressions of the target genes KIT, SPO11 and ACRV1 in the testis tissue of the NOA males compared with those in the OA patients (P<0.01).

Conclusion: The levels of NSD1 and H3K36me2 are decreased in testis tissue of the NOA patient, H3K36me2 is highly enriched in the spermatogenesis-related key genes KIT, SPO11 and ACRV1, and the down-regulated expression of NSD1 impairs spermatogenesis.

[NSD1在非阻塞性无精子症发病机制中调控H3K36me2]。
目的:探讨核受体结合SET-domain蛋白1 (NSD1)通过调控相关基因的表达在非阻塞性无精子症(NOA)发病中的作用。方法:采用qPCR和免疫荧光法检测7例男性阻塞性无精子症(OA)和18例NOA患者睾丸组织中NSD1的表达,并采用免疫荧光染色、Western blot和免疫沉淀(IP)法检测两组患者睾丸组织中H3K36me2的修饰水平。我们通过染色质IP-based sequencing (ChIP-Seq)检测了H3K36me2在睾丸组织中的富集差异,利用生物信息学分析了H3K36me2的基因组分布和靶基因,并通过qPCR验证了两组患者睾丸中靶基因的表达水平。结果:与OA患者相比,NOA患者NSD1 mRNA和蛋白表达明显降低(P=0.000 8)。在两组患者的睾丸组织中均观察到NSD1与H3K36me2的结合,而在NOA男性中H3K36me2的修饰水平明显降低。两组患者的睾丸中H3K36me2主要分布在基因间区,但NOA组H3K36me2的富集程度明显降低。不同的h3k36me2富集基因参与多种生物过程,包括组织发育和细胞形态发生。ChIP-Seq和qPCR结果显示,与OA患者相比,NOA男性睾丸组织中靶基因KIT、SPO11和ACRV1的表达明显下调(p)。结论:NOA患者睾丸组织中NSD1和H3K36me2表达水平降低,H3K36me2高度富集与精子发生相关的关键基因KIT、SPO11和ACRV1, NSD1表达下调损害精子发生。
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来源期刊
中华男科学杂志
中华男科学杂志 Medicine-Medicine (all)
CiteScore
0.40
自引率
0.00%
发文量
5367
期刊介绍: National journal of andrology was founded in June 1995. It is a core journal of andrology and reproductive medicine, published monthly, and is publicly distributed at home and abroad. The main columns include expert talks, monographs (basic research, clinical research, evidence-based medicine, traditional Chinese medicine), reviews, clinical experience exchanges, case reports, etc. Priority is given to various fund-funded projects, especially the 12th Five-Year National Support Plan and the National Natural Science Foundation funded projects. This journal is included in about 20 domestic databases, including the National Science and Technology Paper Statistical Source Journal (China Science and Technology Core Journal), the Source Journal of the China Science Citation Database, the Statistical Source Journal of the China Academic Journal Comprehensive Evaluation Database (CAJCED), the Full-text Collection Journal of the China Journal Full-text Database (CJFD), the Overview of the Chinese Core Journals (2017 Edition), and the Source Journal of the Top Academic Papers of China's Fine Science and Technology Journals (F5000). It has been included in the full text of the American Chemical Abstracts, the American MEDLINE, the American EBSCO, and the database.
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