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长链非编码 RNA-Gm2044 可被 A-MYB 转录激活,并作为 miR-335-3p 的海绵调节 Sycp1 的表达,在小鼠精母细胞源性 GC-2spd(ts) 细胞中发挥作用。

LncRNA-Gm2044 is transcriptionally activated by A-MYB and regulates Sycp1 expression as a miR-335-3p sponge in mouse spermatocyte-derived GC-2spd(ts) cells.

机构信息

School of Life Science, Bengbu Medical College, Bengbu, Anhui, People's Republic of China.

School of Life Science, Bengbu Medical College, Bengbu, Anhui, People's Republic of China.

出版信息

Differentiation. 2020 Jul-Aug;114:49-57. doi: 10.1016/j.diff.2020.05.004. Epub 2020 May 19.

Abstract

Long noncoding RNAs (lncRNAs) have been shown to execute key roles in spermatogenesis. However, little is known about how lncRNAs gene expression is itself regulated in the germ cells of testis. We previously demonstrated that high expression of lncRNA-Gm2044 exists in spermatocytes and can regulate male germ cell proliferation. Here, the transcriptional regulation of lnRNA-Gm2044 expression in spermatocytes and the downstream signaling were further explored. A bioinformatics assessment predicted two potential binding-sites for the spermatocyte-specific transcription factor A-MYB in the promoter region of lncRNA-Gm2044. Our results proved that the transcription factor A-MYB promotes the expression of lncRNA-Gm2044 in mouse spermatocyte-derived GC-2spd(ts) cells. ChIP and luciferase assays verified that A-MYB mainly binds to the distal promoter region (-819 bp relative to the transcription start site) of lncRNA-Gm2044 and regulates lncRNA-Gm2044 expression through the -819 bp binding-site. In addition, we confirmed that lncRNA-Gm2044 functions as a miR-335-3p sponge to enhance the levels of miR-335-3p's direct target protein, Sycp1. Furthermore, A-MYB can up-regulate Sycp1 expression and down-regulate GC-2spd(ts) cell proliferation by activating its target, lncRNA-Gm2044. Overexpression of lncRNA-Gm2044 or knockdown of miR-335-3p can, at least partially, rescue the effects of A-MYB on Sycp1 expression and GC-2spd(ts) cell proliferation.Taken together, our results provide new information on the mechanistic roles of lncRNA-miRNA in transcription factor A-MYB regulation of spermatocyte function.

摘要

长链非编码 RNA(lncRNAs)在精子发生中发挥关键作用已得到证实。然而,lncRNAs 基因表达本身在睾丸生殖细胞中是如何被调控的还知之甚少。我们之前的研究表明,lncRNA-Gm2044 在精母细胞中高表达,并能调节雄性生殖细胞的增殖。在这里,我们进一步探讨了 lncRNA-Gm2044 在精母细胞中的转录调控及其下游信号通路。生物信息学评估预测,lncRNA-Gm2044 启动子区存在两个潜在的与精母细胞特异性转录因子 A-MYB 结合的位点。我们的结果证明,转录因子 A-MYB 促进了小鼠精母细胞源性 GC-2spd(ts)细胞中 lncRNA-Gm2044 的表达。ChIP 和荧光素酶报告基因检测证实,A-MYB 主要结合于 lncRNA-Gm2044 启动子的远端(相对于转录起始位点-819bp),并通过-819bp 结合位点调节 lncRNA-Gm2044 的表达。此外,我们证实 lncRNA-Gm2044 作为 miR-335-3p 的海绵体,增强了 miR-335-3p 的直接靶蛋白 Sycp1 的水平。此外,A-MYB 可以通过激活其靶基因 lncRNA-Gm2044,上调 Sycp1 表达并下调 GC-2spd(ts)细胞增殖。lncRNA-Gm2044 的过表达或 miR-335-3p 的敲低至少可以部分挽救 A-MYB 对 Sycp1 表达和 GC-2spd(ts)细胞增殖的影响。综上所述,我们的研究结果为 lncRNA-miRNA 在转录因子 A-MYB 调控精母细胞功能中的作用机制提供了新的信息。

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