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小鼠精原细胞中的下调通过/发挥作用。

Downregulation in Mouse Spermatogonia Functions through /.

作者信息

Gao Hongmei, Zhang Mingrui, Guo Jiankang, Liu Zhiguo, Guo Fei, Wang Bingyuan, Mu Yulian

机构信息

Institute of Animal Sciences, Chinese Academy of Agricultural Sciences, Beijing 100193, China.

College of Animal Science and Technology, China Agricultural University, Beijing 100193, China.

出版信息

Life (Basel). 2022 Aug 5;12(8):1194. doi: 10.3390/life12081194.

Abstract

Protein arginine methyltransferases 7 () is expressed in male germ cells, including primordial germ cells, gonocytes, and spermatogonia. Our previous study demonstrated that downregulation reduced the proliferation of GC-1 cells (a cell line of mouse immortalized spermatogonia). However, how regulates spermatogonial proliferation through miRNA and the target gene remains elusive. Here, we experimentally reduced the expression in the GC-1 cells and subjected them to miRNA sequencing to explore the miRNA profile and its -responsive members. In total, 48 differentially expressed miRNAs (DEmiRNAs), including 36 upregulated and 12 downregulated miRNAs, were identified. After verifying the validity of sequencing results through qRT-PCR assays in randomly selected DEmiRNAs, we predicted the target genes of these DEmiRNAs. Next, we combined DEmiRNA target genes and previously identified differentially expressed genes between knockdown and control groups of GC-1 cells, which resulted in seven miRNA/target gene pairs. Among these miRNA/target gene pairs, we further detected the expression of (collagen type VI alpha 3) as the target gene of . The results suggested that downregulation in mouse spermatogonia might function through /. Overall, these findings provide new insights into the role of in male germ cell development through miRNA and target genes.

摘要

蛋白质精氨酸甲基转移酶7(PRMT7)在雄性生殖细胞中表达,包括原始生殖细胞、生殖母细胞和精原细胞。我们之前的研究表明,PRMT7下调会降低GC-1细胞(一种小鼠永生化精原细胞系)的增殖。然而,PRMT7如何通过miRNA和靶基因调节精原细胞增殖仍不清楚。在这里,我们通过实验降低了GC-1细胞中PRMT7的表达,并对其进行miRNA测序,以探索miRNA谱及其PRMT7反应性成员。总共鉴定出48个差异表达的miRNA(DEmiRNA),包括36个上调的和12个下调的miRNA。在通过对随机选择的DEmiRNA进行qRT-PCR分析验证测序结果的有效性后,我们预测了这些DEmiRNA的靶基因。接下来,我们将DEmiRNA靶基因与先前鉴定的GC-1细胞PRMT7敲低组和对照组之间差异表达的基因相结合,得到了7个miRNA/靶基因对。在这些miRNA/靶基因对中,我们进一步检测了作为miR-145-5p靶基因的Col6a3(VI型胶原蛋白α3)的表达。结果表明,小鼠精原细胞中PRMT7下调可能通过miR-145-5p/Col6a3发挥作用。总体而言,这些发现为PRMT7通过miRNA和靶基因在雄性生殖细胞发育中的作用提供了新的见解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/59ee/9410080/47eefad8ccc0/life-12-01194-g001.jpg

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