Department of Comparative Medicine, King Faisal Specialist Hospital & Research Centre, P.O. Box 3354, Riyadh, 11211, Saudi Arabia.
College of Medicine, Alfaisal University, Riyadh, 11533, Saudi Arabia.
Sci Rep. 2022 Dec 12;12(1):21456. doi: 10.1038/s41598-022-25826-7.
During mammalian spermatogenesis, the ubiquitin proteasome system maintains protein homoeostasis (proteastasis) and spermatogenic cellular functions. DCAF17 is a substrate receptor in the ubiquitin CRL4 E3 Ligase complex, absence of which causes oligoasthenoteratozoospermia in mice resulting in male infertility. To determine the molecular phenomenon underlying the infertility phenotype caused by disrupting Dcaf17, we performed RNA-sequencing-based gene expression profiling of 3-weeks and 8-weeks old Dcaf17 wild type and Dcaf17 disrupted mutant mice testes. At three weeks, 44% and 56% differentially expressed genes (DEGs) were up- and down-regulated, respectively, with 32% and 68% DEGs were up- and down-regulated, respectively at 8 weeks. DEGs include protein coding genes and lncRNAs distributed across all autosomes and the X chromosome. Gene ontology analysis revealed major biological processes including proteolysis, regulation of transcription and chromatin remodelling are affected due to Dcaf17 disruption. We found that Dcaf17 disruption up-regulated several somatic genes, while germline-associated genes were down-regulated. Up to 10% of upregulated, and 12% of downregulated, genes were implicated in male reproductive phenotypes. Moreover, a large proportion of the up-regulated genes were highly expressed in spermatogonia and spermatocytes, while the majority of downregulated genes were predominantly expressed in round spermatids. Collectively, these data show that the Dcaf17 disruption affects directly or indirectly testicular proteastasis and transcriptional signature in mouse.
在哺乳动物精子发生过程中,泛素蛋白酶体系统维持蛋白质的同型平衡(蛋白质稳态)和精子发生的细胞功能。DCAF17 是泛素 CRL4 E3 连接酶复合物中的底物受体,其缺失会导致小鼠少精症、弱精症和畸形精子症,从而导致男性不育。为了确定破坏 Dcaf17 引起不育表型的分子现象,我们对 3 周和 8 周龄 Dcaf17 野生型和 Dcaf17 缺失突变型小鼠睾丸进行了基于 RNA-seq 的基因表达谱分析。在 3 周时,分别有 44%和 56%的差异表达基因(DEGs)上调和下调,而在 8 周时,分别有 32%和 68%的 DEGs 上调和下调。DEGs 包括分布在所有常染色体和 X 染色体上的蛋白质编码基因和 lncRNA。基因本体论分析显示,主要的生物学过程包括蛋白酶解、转录调控和染色质重塑受到 Dcaf17 缺失的影响。我们发现 Dcaf17 缺失会上调几个体细胞基因,而生殖细胞相关基因则下调。多达 10%的上调基因和 12%的下调基因与男性生殖表型有关。此外,上调基因中有很大一部分在精原细胞和精母细胞中高表达,而大多数下调基因主要在圆形精子细胞中表达。总之,这些数据表明,Dcaf17 缺失直接或间接影响小鼠睾丸的蛋白质稳态和转录特征。