He Haihong, Yu Fan, Shen Wang, Chen Keyan, Zhang Lijun, Lou Shuang, Zhang Qiaomin, Chen Siping, Yuan Xinhua, Jia Xingwang, Zhou Yiwen
Department of Emergency Laboratory, Clinical Laboratory Medical Center, Shenzhen Hospital, Southern Medical University, Shenzhen, China.
Department of Clinical Laboratory, Affiliated Jiangmen TCM Hospital of Ji'nan University, Jiangmen, China.
Front Genet. 2021 Feb 26;12:608629. doi: 10.3389/fgene.2021.608629. eCollection 2021.
Non-obstructive azoospermia (NOA) is one of the most important causes of male infertility. It is mainly characterized by the absence of sperm in semen repeatedly or the number of sperm is small and not fully developed. At present, its pathogenesis remains largely unknown. The goal of this study is to identify hub genes that might affect biomarkers related to spermatogenesis. Using the clinically significant transcriptome and single-cell sequencing data sets on the Gene Expression Omnibus (GEO) database, we identified candidate hub genes related to spermatogenesis. Based on them, we performed Gene Ontology (GO) functional enrichment analysis, Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment pathway analyses, protein-protein interaction (PPI) network analysis, principal component analysis (PCA), cell cluster analysis, and pseudo-chronological analysis. We identified a total of 430 differentially expressed genes, of which three have not been reported related to spermatogenesis (C22orf23, TSACC, and TTC25), and the expression of these three hub genes was different in each type of sperm cells. The results of the pseudo-chronological analysis of the three hub genes indicated that TTC25 was in a low expression state during the whole process of sperm development, while the expression of C22orf23 had two fluctuations in the differentiating spermatogonia and late primary spermatocyte stages, and TSACC showed an upward trend from the spermatogonial stem cell stage to the spermatogenesis stage. Our research found that the three hub genes were different in the trajectory of sperm development, indicating that they might play important roles in different sperm cells. This result is of great significance for revealing the pathogenic mechanism of NOA and further research.
非梗阻性无精子症(NOA)是男性不育的最重要原因之一。其主要特征是精液中反复无精子或精子数量少且发育不全。目前,其发病机制在很大程度上仍不清楚。本研究的目的是识别可能影响与精子发生相关生物标志物的枢纽基因。利用基因表达综合数据库(GEO)上具有临床意义的转录组和单细胞测序数据集,我们确定了与精子发生相关的候选枢纽基因。基于这些基因,我们进行了基因本体(GO)功能富集分析、京都基因与基因组百科全书(KEGG)富集通路分析、蛋白质-蛋白质相互作用(PPI)网络分析、主成分分析(PCA)、细胞聚类分析和拟时序分析。我们共鉴定出430个差异表达基因,其中三个与精子发生相关的基因尚未见报道(C22orf23、TSACC和TTC25),这三个枢纽基因在每种类型的精子细胞中的表达均不同。对这三个枢纽基因的拟时序分析结果表明,TTC25在精子发育全过程中处于低表达状态,而C22orf23在精原细胞分化期和初级精母细胞后期有两个表达波动,TSACC从精原干细胞阶段到精子发生阶段呈上升趋势。我们的研究发现,这三个枢纽基因在精子发育轨迹上存在差异,表明它们可能在不同的精子细胞中发挥重要作用。这一结果对于揭示NOA的发病机制及进一步研究具有重要意义。