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Jun 介导的长非编码 RNA-IMS 通过 gga-miR-31-5p/stra8 促进鸡精原干细胞的减数分裂。

Jun-mediated lncRNA-IMS promotes the meiosis of chicken spermatogonial stem cells via gga-miR-31-5p/stra8.

机构信息

College of Biotechnology, Jiangsu University of Science and Technology, Zhenjiang, Jiangsu Province, People's Republic of China.

Jiangsu Province Key Laboratory of Animal Breeding and Molecular Design, College of Animal Science and Technology, Yangzhou University, Yangzhou Province, People's Republic of China.

出版信息

Mol Reprod Dev. 2023 May;90(5):275-286. doi: 10.1002/mrd.23682. Epub 2023 Mar 26.

Abstract

Meiosis, a key step in spermatogenesis, is affected by many factors. Current studies have shown that long noncoding RNAs (lncRNAs) are potential factors regulating meiosis, and their regulatory mechanisms have received much attention. However, little research has been done on its regulatory mechanism in the spermatogenesis of roosters. Here, we found that lncRNA involved in meiosis and spermatogenesis (lncRNA-IMS) was involved in the regulation of Stra8 by gga-miR-31-5p and hindered the inhibition of Stra8 by gga-miR-31-5p. The acquisition and loss of function experiments demonstrated that lncRNA-IMS was involved in meiosis and spermatogenesis. In addition, we predicted and determined the core promoter region of lncRNA-IMS. Prediction of transcription factors, deletion/overexpression of binding sites, knockdown/overexpression of Jun, and dual-luciferase reporter analysis confirmed that Jun positively activated transcription of lncRNA-IMS. Our findings further enrich the TF-lncRNA-miRNA-mRNA regulatory network during male meiosis and provide new ideas for studying the molecular mechanism of meiosis and spermatogenesis in chicken spermatogonial stem cells.

摘要

减数分裂是精子发生的关键步骤,受许多因素的影响。目前的研究表明,长链非编码 RNA(lncRNA)是调节减数分裂的潜在因素,其调节机制受到了广泛关注。然而,关于其在公鸡精子发生中的调节机制的研究甚少。在这里,我们发现参与减数分裂和精子发生的 lncRNA(lncRNA-IMS)参与了gga-miR-31-5p 对 Stra8 的调节,并阻碍了 gga-miR-31-5p 对 Stra8 的抑制。获得和丧失功能实验表明 lncRNA-IMS 参与了减数分裂和精子发生。此外,我们预测并确定了 lncRNA-IMS 的核心启动子区域。转录因子的预测、结合位点的缺失/过表达、Jun 的敲低/过表达以及双荧光素酶报告分析证实了 Jun 对 lncRNA-IMS 的转录具有正激活作用。我们的研究结果进一步丰富了男性减数分裂过程中 TF-lncRNA-miRNA-mRNA 调控网络,为研究鸡精原干细胞减数分裂和精子发生的分子机制提供了新的思路。

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