揭示无精子症的遗传基础:希腊人群的 RNA 序列和转录组特征分析。

Alexandra Chatziparasidou, Theologia Sarafidou, Maria-Anna Kyrgiafini, Katerina Moutou, Maria Markantoni, Themistoklis Giannoulis, Achilleas Papatheodorou, Chara Oraiopoulou, Glykeria Samolada, Nikos Christoforidis, Zissis Mamuris
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引用次数: 0

摘要

目的研究特发性非梗阻性无精子症(iNOA)是否有自己的转录组特征:设计:对 26 名经同意诊断为特发性非梗阻性无精子症(iNOA)的患者的睾丸组织活检样本进行检索、处理并准备提取 RNA。根据睾丸精子的存在情况将样本分为四个池:两个 "无精子存在 "池(Null-spz-1 和 Null-spz-2 池)、一个 "高精子存在 "池(High-spz 池)和一个 "罕见精子存在 "池(Rare-spz 池)。第二组复制池(CF-1 和 CF-2)来自梗阻性无精子症(OA)患者,作为对照。进行了 RNA 测序(RNA-seq)和比较转录组学分析(CTA),然后只对蛋白编码基因进行了差异基因表达分析(DGE)。使用基因本体(GO)、STRING和京都基因组百科全书(KEGG)生物信息平台进一步分析了专门上调或下调的差异表达基因(DEGs):受试者:确诊为 iNOA 的男性。暴露:确诊为 iNOA 的男性的睾丸活检组织:主要结果指标:蛋白质编码差异表达基因(DEGs):结果:在患有 iNOA 的男性的睾丸组织中,蛋白质编码基因的转录组概况发生了明显改变。共有 3858 个基因表现出表达失调,其中 1994 个基因完全下调,1734 个基因上调。下调的 DEGs 显著富集了雄性配子生成(GO:0048232)和减数分裂周期(GO:0051321)等生物过程(BPs),而上调的 DEGs 则富集了细胞死亡调控(GO:0010941)、细胞粘附调控(GO:0030155)和防御反应(GO:0006952)等生物过程(BPs)。互作组分析确定了下调 DEGs 中的枢纽基因,包括 PCNA、PLK1、MCM4、CDK1、CCNB1、AURKA、CCNA2 和 CDC6,以及上调 DEGs 中的枢纽基因,包括表皮生长因子受体、RELA、CTNNB1、MYC、JUN、SMAD3、STAT3 NFKB1、TGFB1 和 ACTB。此外,KEGG分析表明,下调基因主要影响细胞周期(hsa04110)和卵母细胞减数分裂(hsa04114)等通路,而上调基因主要影响病灶粘附(hsa04510)和PI3-Akt信号通路(hsa04151)等通路:结论:在患有 iNOA 的男性睾丸组织中发现了独特的 mRNA 表达谱和转录组活性的改变。
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Unraveling the genetic basis of azoospermia: transcriptome profiling analyses in a Greek population.

Objective: To investigate whether idiopathic nonobstructive azoospermia (iNOA) has its own transcriptomic signature.

Design: Testicular tissue biopsies were retrieved, processed, and prepared for ribonucleic acid (RNA) extraction from 26 consented patients diagnosed with iNOA. Samples were grouped into four pools based on the presence of testicular spermatozoa: two replicate pools for "No presence" (Null-spz-1 and Null-spz-2 pools), one for "High presence" (High-spz pool), and one for "Rare presence" (Rare-spz pool). A second set of replicate pools (CF-1 and CF-2) were used from patients with obstructive azoospermia (OA) and served as controls. RNA sequencing (RNA-seq) and comparative transcriptomics analysis were performed, followed by differential gene expression analysis focused on protein-coding genes only. Differentially expressed genes (DEGs) exclusively upregulated or downregulated were further analyzed using the Gene Ontology (GO), STRING, and Kyoto Encyclopedia of Genes and Genome bioinformatic platforms.

Setting: Private Fertility Clinic and Public University.

Patients: Males in whom iNOA was diagnosed.

Exposure: Testicular biopsies from men in whom iNOA was diagnosed.

Main outcome measures: Protein-coding DEGs.

Results: A significantly altered transcriptomic profile of protein-coding genes was identified in the testicular tissues from men with iNOA. A total of 3,858 genes exhibited dysregulated expression, with 1,994 genes being exclusively downregulated and 1,734 upregulated. Biological processes such as male gamete generation (GO:0048232) and meiotic cycle (GO:0051321) were significantly enriched by the downregulated DEGs whereas the upregulated DEGs enriched BPs such as regulation of cell death (GO:0010941), regulation of cell adhesion (GO:0030155), and defense response (GO:0006952). Interactome analysis identified hub genes among the downregulated DEGs, including PCNA, PLK1, MCM4, CDK1, CCNB1, AURKA, CCNA2, and CDC6, and among the upregulated DEGs, including EGFR, RELA, CTNNB1, MYC, JUN, SMAD3, STAT3 NFKB1, TGFB1, and ACTB. In addition, Kyoto Encyclopedia of Genes and Genome analysis demonstrated that pathways such as cell cycle (hsa04110) and oocyte meiosis (hsa04114) are primarily affected by the downregulated genes, whereas the upregulated genes mainly affected pathways such as the focal adhesion (hsa04510) and the PI3-Akt signaling pathway (hsa04151).

Conclusion: A distinct messenger RNA expression profile and altered transcriptomic activity were identified in the testicular tissues of men with iNOA.

Clinical trial registration number: University of Thessaly 1, 15.04.2016 and the Greek National Authority 701/15.9.2017.

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来源期刊
F&S science
F&S science Endocrinology, Diabetes and Metabolism, Obstetrics, Gynecology and Women's Health, Urology
CiteScore
2.00
自引率
0.00%
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0
审稿时长
51 days
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