Department of Physiology, Anatomy and Microbiology, School of Life Sciences, La Trobe University, Bundoora, Victoria, Australia.
Bioinformatics and Expression Analysis core facility, Department of Biosciences and Nutrition, Karolinska Institutet, Stockholm, Sweden.
Dev Dyn. 2020 Dec;249(12):1500-1513. doi: 10.1002/dvdy.254. Epub 2020 Oct 6.
The transcription factor pleomorphic adenoma gene 1 (PLAG1) is required for male fertility. Mice deficient in PLAG1 exhibit decreased sperm motility and abnormal epididymal tubule elongation and coiling, indicating impaired sperm maturation during epididymal transit. However, the downstream transcriptomic profile of the Plag1 knockout (KO; Plag1 ) murine epididymis is currently unknown.
In this study, the PLAG1-dependent epididymal transcriptome was characterised using RNA sequencing. Several genes important for the control of sperm maturation, motility, capacitation and the acrosome reaction were dysregulated in Plag1 mice. Surprisingly, several cell proliferation genes were upregulated, and Ki67 analysis indicated that cell proliferation is aberrantly upregulated in the cauda epididymis stroma of Plag1 mice. Gene ontology analysis showed an overall upregulation of genes encoding extracellular matrix components, and an overall downregulation of genes encoding metalloendopeptidases in the epididymides from Plag1 mice.
Together, these results suggest a defect in the epididymal extracellular matrix in Plag1 mice. These results imply that in addition to maintaining epididymal integrity directly, PLAG1 may also regulate several genes involved in the regulation of sperm maturation and capacitation. Moreover, PLAG1 may also be involved in regulating tissue homeostasis and ensuring proper structure and maintenance of the extracellular matrix in the epididymis.
转录因子多形性腺瘤基因 1(PLAG1)是雄性生育所必需的。PLAG1 缺失的小鼠表现出精子运动能力下降和附睾小管伸长和卷曲异常,表明附睾转运过程中精子成熟受损。然而,目前尚不清楚 Plag1 敲除(KO;Plag1 )小鼠附睾的下游转录组图谱。
在这项研究中,使用 RNA 测序对 PLAG1 依赖的附睾转录组进行了表征。在 Plag1 小鼠中,几个对精子成熟、运动、获能和顶体反应控制重要的基因失调。令人惊讶的是,几个细胞增殖基因上调,Ki67 分析表明 Plag1 小鼠附睾尾部间质的细胞增殖异常上调。基因本体分析显示,Plag1 小鼠附睾中编码细胞外基质成分的基因总体上调,编码金属内肽酶的基因总体下调。
总之,这些结果表明 Plag1 小鼠的附睾细胞外基质存在缺陷。这些结果表明,PLAG1 除了直接维持附睾完整性外,还可能调节几个参与精子成熟和获能调节的基因。此外,PLAG1 还可能参与调节组织稳态,并确保附睾细胞外基质的适当结构和维持。