Shi Kesong, Wang Baoluri, Dou Le, Wang Shu, Fu Xinrui, Yu Haiquan
State Key Laboratory of Reproductive Regulation and Breeding of Grassland Livestock (RRBGL), Inner Mongolia University, Hohhot, China.
Front Physiol. 2022 Dec 8;13:949486. doi: 10.3389/fphys.2022.949486. eCollection 2022.
induction of spermatogonial stem cells (SSCs) from embryonic stem cells (ESCs) provides a promising tool for the treatment of male infertility. A variety of molecules are involved in this complex process, which needs to be further clarified. Undoubtedly, the increased knowledge of SSC formation will be beneficial to facilitate the currently complex induction process. Based on ATAC-seq, DNase-seq, RNA-seq, and microarray data from GEO datasets, chromatin property data (ATAC-seq, DNase-seq) and gene expression data (RNA-seq, microarray data) were combined to search for SSC-specific transcription factors (TFs) and hub SSC-specific genes by using the WGCNA method. Then, we applied RNA-seq and microarray data screening for key SSC-specific TFs and constructed key SSC-specific TF-mediated gene regulatory networks (GRNs) using ChIP-seq data. First, after analysis of the ATAC-seq and DNase-seq data of mouse ESCs, primordial germ cells (PGCs), and SSCs, 33 SSC-specific TFs and 958 targeting genes were obtained. RNA-seq and WGCNA revealed that the key modules (turquoise and red) were the most significantly related to 958 SSC-specific genes, and a total of 10 hub SSC-specific genes were identified. Next, when compared with the cell-specific TFs in human ESCs, PGCs, and SSCs, we obtained five overlapping SSC-specific TF motifs, including the NF1 family TF motifs (NFIA, NFIB, NFIC, and NFIX), GRE, Fox:Ebox, PGR, and ARE. Among these, and exhibited abnormally high expression levels relative to mouse ESCs and PGCs. Moreover, and were upregulated in the testis sample with impaired spermatogenesis when compared with the normal group. Finally, the ChIP-seq data results showed that NFIB most likely targeted the hub SSC-specific genes of the turquoise module (, , , , and ) and the red module ( and ). Our findings preliminarily revealed cell-specific TFs and cell-specific TF-mediated GRNs in the process of SSC formation. The hub SSC-specific genes and the key SSC-specific TFs were identified and suggested complex network regulation, which may play key roles in optimizing the induction efficiency of the differentiation of ESCs into SSCs .
从胚胎干细胞(ESC)诱导生成精原干细胞(SSC)为治疗男性不育提供了一种有前景的工具。多种分子参与了这一复杂过程,这一过程仍需进一步阐明。毫无疑问,对SSC形成的深入了解将有助于简化当前复杂的诱导过程。基于来自GEO数据集的ATAC-seq、DNase-seq、RNA-seq和微阵列数据,结合染色质特性数据(ATAC-seq、DNase-seq)和基因表达数据(RNA-seq、微阵列数据),使用WGCNA方法寻找SSC特异性转录因子(TF)和核心SSC特异性基因。然后,我们应用RNA-seq和微阵列数据筛选关键的SSC特异性TF,并利用ChIP-seq数据构建关键的SSC特异性TF介导的基因调控网络(GRN)。首先,在分析小鼠ESC、原始生殖细胞(PGC)和SSC的ATAC-seq和DNase-seq数据后,获得了33个SSC特异性TF和958个靶向基因。RNA-seq和WGCNA显示关键模块(绿松石色和红色)与958个SSC特异性基因的相关性最显著,共鉴定出10个核心SSC特异性基因。接下来,与人类ESC、PGC和SSC中的细胞特异性TF进行比较时,我们获得了五个重叠的SSC特异性TF基序,包括NF1家族TF基序(NFIA、NFIB、NFIC和NFIX)、GRE、Fox:Ebox、PGR和ARE。其中, 和 相对于小鼠ESC和PGC表现出异常高的表达水平。此外,与正常组相比, 和 在精子发生受损的睾丸样本中上调。最后,ChIP-seq数据结果表明,NFIB最有可能靶向绿松石色模块( 、 、 、 和 )和红色模块( 和 )的核心SSC特异性基因。我们的研究结果初步揭示了SSC形成过程中的细胞特异性TF和细胞特异性TF介导的GRN。鉴定出了核心SSC特异性基因和关键的SSC特异性TF,并提示了复杂的网络调控,这可能在优化ESC向SSC分化的诱导效率中起关键作用。