Ozsait-Selcuk Bilge, Bulgurcuoglu-Kuran Sibel, Sever-Kaya Dilek, Coban Neslihan, Aktan Gulsen, Kadioglu Ates
Department of Genetics, Aziz Sancar Institute of Experimental Medicine, Istanbul University, Istanbul 34093, Türkiye.
Department of Medical Genetics, Istanbul Faculty of Medicine, Istanbul University, Istanbul 34093, Türkiye.
Asian J Androl. 2025 Jan 1;27(1):76-83. doi: 10.4103/aja202452. Epub 2024 Aug 27.
Spermatozoa have a highly complex RNA profile. Several of these transcripts are suggested as biomarkers for male infertility and contribute to early development. To analyze the differences between sperm RNA quantity and expression of protamine ( PRM1 and PRM2 ) and testis-specific histone 2B ( TH2B ) genes, spermatozoa from 33 patients who enrolled in assisted reproduction treatment (ART) program were analyzed. Sperm RNA of teratozoospermic (T), oligoteratozoospermic (OT), and normozoospermic (N) samples was extracted, and the differences in transcript levels among the study groups were analyzed by quantitative real-time polymerase chain reaction (qRT-PCR). The correlations of total RNA per spermatozoon and the expression of the transcripts were evaluated in relation to sperm characteristics and preimplantation embryo development. The mean (±standard deviation) RNA amount per spermatozoon was 28.48 (±23.03) femtogram in the overall group and was significantly higher in the OT group than that in N and T groups. Total sperm RNA and gene expression of PRM1 and PRM2 genes were related to preimplantation embryo development and developmental arrest. Specific sperm characteristics were correlated with the expressions of PRM1 , PRM2 , or TH2B genes. We conclude that the sperm RNA amount and composition are important factors and might influence early embryonic development and also differ in different cases of male infertility.
精子具有高度复杂的RNA图谱。其中一些转录本被认为是男性不育的生物标志物,并对早期发育有贡献。为了分析精子RNA数量与鱼精蛋白(PRM1和PRM2)及睾丸特异性组蛋白2B(TH2B)基因表达之间的差异,对33名参加辅助生殖治疗(ART)项目的患者的精子进行了分析。提取了畸形精子症(T)、轻度畸形精子症(OT)和正常精子症(N)样本的精子RNA,并通过定量实时聚合酶链反应(qRT-PCR)分析了研究组之间转录水平的差异。评估了每个精子的总RNA与转录本表达之间与精子特征和植入前胚胎发育的相关性。整个组中每个精子的平均(±标准差)RNA量为28.48(±23.03)飞克,OT组显著高于N组和T组。精子总RNA以及PRM1和PRM2基因的表达与植入前胚胎发育和发育停滞有关。特定的精子特征与PRM1、PRM2或TH2B基因的表达相关。我们得出结论,精子RNA的数量和组成是重要因素,可能影响早期胚胎发育,并且在不同的男性不育病例中也存在差异。