Suppr超能文献

Dlk1-Dio3印记区域长链非编码RNA的表达模式及囊胚发育过程中Gtl2激活的潜在机制。

Expression patterns of long noncoding RNAs from Dlk1-Dio3 imprinted region and the potential mechanisms of Gtl2 activation during blastocyst development.

作者信息

Han Zhengbin, Yu Changwei, Tian Yijun, Zeng Tiebo, Cui Wei, Mager Jesse, Wu Qiong

机构信息

Harbin Institute of Technology, School of Life Science and Technology, State Key Laboratory of Urban Water Resources and Environment, Harbin 150080, China; University of Massachusetts, Veterinary and Animal Science Department, 661 North Pleasant Street, Amherst, MA 01003, USA.

Harbin Institute of Technology, School of Life Science and Technology, State Key Laboratory of Urban Water Resources and Environment, Harbin 150080, China.

出版信息

Biochem Biophys Res Commun. 2015 Jul 31;463(3):167-73. doi: 10.1016/j.bbrc.2015.04.126. Epub 2015 May 22.

Abstract

The function of long noncoding RNAs (lncRNAs) in cell differentiation and development have begun to be revealed in recent years. However, the expression pattern and mechanisms regulating lncRNAs are largely unknown during mammalian preimplantation development. LncRNAs expressed from Dlk1-Dio3 imprinted region have been linked to pluripotency of induced pluripotent cells (iPSCs). In this study we show that these lncRNAs (Gtl2, Rian and Mirg) are first expressed at the morula stage and gradually restricted to the inner cell mass (ICM) as the embryo differentiates into the blastocyst. Analysis of DNA methylation at IG-DMR and Gtl2-DMR showed no change during preimplantation while the presence of the activating histone modification H3K4me3 increased significantly from 8-cell to blastocyst stage, which may explain the expression activation. Additionally, knockdown of transcription factors (Oct4, Sox2 and Nanog) in blastocyst reduced the expression of Gtl2, indicating pluripotency factors regulate transcription of these lncRNAs. This study provides the spatiotemporal expression and dynamic changes of lncRNAs from Dlk1-Dio3 imprinted region in mouse preimplantation stage embryos and offers insight into the potential mechanisms responsible for Gtl2 activation.

摘要

近年来,长链非编码RNA(lncRNA)在细胞分化和发育中的功能已开始被揭示。然而,在哺乳动物着床前发育过程中,lncRNA的表达模式和调控机制仍 largely未知。从Dlk1-Dio3印记区域表达的lncRNA已与诱导多能干细胞(iPSC)的多能性相关联。在本研究中,我们表明这些lncRNA(Gtl2、Rian和Mirg)首先在桑椹胚阶段表达,并随着胚胎分化为囊胚而逐渐局限于内细胞团(ICM)。对IG-DMR和Gtl2-DMR处DNA甲基化的分析表明,在着床前阶段没有变化,而激活组蛋白修饰H3K4me3的存在从8细胞期到囊胚期显著增加,这可能解释了表达激活。此外,在囊胚中敲低转录因子(Oct4、Sox2和Nanog)会降低Gtl2的表达,表明多能性因子调节这些lncRNA的转录。本研究提供了小鼠着床前阶段胚胎中来自Dlk1-Dio3印记区域的lncRNA的时空表达和动态变化,并深入了解了负责Gtl2激活的潜在机制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验