Wang Xiaorong, Sang Mengmeng, Gong Shengnan, Chen Zhichuan, Zhao Xi, Wang Guishuan, Li Zhiran, Huang Yingying, Chen Shitao, Xie Gangcai, Duan Enkui, Sun Fei
Institute of Reproductive Medicine, School of Medicine, Nantong University, Nantong, Jiangsu 226001, PR China.
International Peace Maternity and Child Health Hospital, Shanghai Key Laboratory for Reproductive Medicine, School of Medicine, Shanghai Jiaotong University, Shanghai 200030, PR China.
Genes Dis. 2021 Jan 9;9(4):1062-1073. doi: 10.1016/j.gendis.2020.12.012. eCollection 2022 Jul.
As a BET bromodomain inhibitor, JQ1 has been proven have efficacy against a number of different cancers. In terms of male reproduction, JQ1 may be used as a new type of contraceptive, since JQ1 treatment in male mice could lead to germ cell defects and a decrease of sperm motility, moreover, this effect is reversible. However, the mechanism of JQ1 acting on gene regulation in spermatogenesis remains unclear. Here, we performed single-cell RNA sequencing (scRNA-seq) on mouse testes treated with JQ1 or vehicle control to determine the transcriptional regulatory function of JQ1 in spermatogenesis at the single cell resolution. We confirmed that JQ1 treatment could increase the numbers of somatic cells and spermatocytes and decrease the numbers of spermatid cells. Gene Ontology (GO) analysis demonstrated that differentially expressed genes which were down-regulated after JQ1 injection were mainly enriched in "DNA conformation change" biological process in early developmental germ cells and "spermatid development" biological process in spermatid cells. ATAC-seq data further confirmed that JQ1 injection could change the open state of chromatin. In addition, JQ1 could change the numbers of accessible meiotic DNA double-stranded break sites and the types of transcription factor motif that functioned in pachytene spermatocytes and round spermatids. The multi-omics analysis revealed that JQ1 had the ability to regulate gene transcription by changing chromatin conformation in mouse spermatogenesis, which would potentiate the availability of JQ1 in male contraceptive.
作为一种BET溴结构域抑制剂,JQ1已被证明对多种不同癌症有效。在男性生殖方面,JQ1可用作新型避孕药,因为对雄性小鼠进行JQ1处理会导致生殖细胞缺陷和精子活力下降,而且这种影响是可逆的。然而,JQ1在精子发生过程中作用于基因调控的机制仍不清楚。在此,我们对用JQ1或载体对照处理的小鼠睾丸进行了单细胞RNA测序(scRNA-seq),以在单细胞分辨率下确定JQ1在精子发生中的转录调控功能。我们证实,JQ1处理可增加体细胞和精母细胞数量,并减少精子细胞数量。基因本体论(GO)分析表明,JQ1注射后下调的差异表达基因主要富集于早期发育生殖细胞中的“DNA构象变化”生物学过程和精子细胞中的“精子细胞发育”生物学过程。ATAC-seq数据进一步证实,JQ1注射可改变染色质的开放状态。此外,JQ1可改变减数分裂期DNA双链断裂位点的可及性数量以及在粗线期精母细胞和圆形精子细胞中起作用的转录因子基序类型。多组学分析表明,JQ1在小鼠精子发生过程中具有通过改变染色质构象来调节基因转录的能力,这将提高JQ1在男性避孕方面的可用性。