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小鼠胚胎干细胞中DRP1抑制后对卵裂期胚胎基因的调控

Regulation of cleavage embryo genes upon DRP1 inhibition in mouse embryonic stem cells.

作者信息

Guo Shi-Meng, Zhang Yi-Ran, Ma Bing-Xin, Zhou Li-Quan, Yin Ying

机构信息

Institute of Reproductive Health, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

Reproductive Medicine Center, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.

出版信息

Front Cell Dev Biol. 2023 May 15;11:1191797. doi: 10.3389/fcell.2023.1191797. eCollection 2023.

Abstract

Dynamic-related protein 1 (DRP1) is a key protein of mitochondrial fission. In this study, we found that inhibition of activity of DRP1 led to increased levels of cleavage embryo genes in mouse embryonic stem cells (mESCs), which might reflect a transient totipotency status derived from pluripotency. This result indicates that DRP1 inhibition in mESCs leads to a tendency to obtain a new expression profile similar to that of the 2C-like state. Meanwhile, we also noticed that the glycolysis/gluconeogenesis pathway and its related enzymes were significantly downregulated, and the key glycolytic enzymes were also downregulated in various 2C-like cells. Moreover, when DRP1 activity was inhibited from the late zygote when cleavage embryo genes started to express, development of early embryos was inhibited, and these cleavage embryo genes failed to be efficiently silenced at the late 2-cell (2C) stage. Taken together, our result shows that DRP1 plays an important role in silencing cleavage embryo genes for totipotency-to-pluripotency transition.

摘要

动力相关蛋白1(DRP1)是线粒体分裂的关键蛋白。在本研究中,我们发现抑制DRP1的活性会导致小鼠胚胎干细胞(mESCs)中卵裂胚胎基因水平升高,这可能反映了源自多能性的短暂全能状态。该结果表明,抑制mESCs中的DRP1会导致获得类似于2C样状态的新表达谱的趋势。同时,我们还注意到糖酵解/糖异生途径及其相关酶显著下调,并且关键糖酵解酶在各种2C样细胞中也下调。此外,当从卵裂胚胎基因开始表达的晚期合子抑制DRP1活性时,早期胚胎的发育受到抑制,并且这些卵裂胚胎基因在晚期2细胞(2C)阶段未能有效沉默。综上所述,我们的结果表明DRP1在沉默卵裂胚胎基因以实现全能性向多能性转变中起重要作用。

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