Linc1548 Promotes the Transition of Epiblast Stem Cells Into Neural Progenitors by Engaging OCT6 and SOX2

Author:

Bai Mingliang1,Li Guoping1,Jiapaer Zeyidan12,Guo Xudong13,Xi Jiajie1,Wang Guiying1,Ye Dan1,Chen Wen1,Duan Baoyu4,Kang Jiuhong1ORCID

Affiliation:

1. Clinical and Translational Research Center of Shanghai First Maternity and Infant Hospital, Shanghai Key Laboratory of Maternal Fetal Medicine, Shanghai Key Laboratory of Signaling and Disease Research, Frontier Science Center for Stem Cell Research, National Stem Cell Translational Resource Center, School of Life Sciences and Technology, Tongji University, Shanghai, People’s Republic of China

2. Xinjiang Key Laboratory of Biology Resources and Genetic Engineering, College of Life Science and Technology, Xinjiang University, Urumqi, People’s Republic of China

3. Institute for Advanced Study, School of Life Sciences and Technology, Tongji University, Shanghai, People’s Republic of China

4. Department of Biochemistry, College of Medical Technology, Shanghai University of Medical and Health Sciences, Shanghai, People’s Republic of China

Abstract

Abstract The transition of embryonic stem cells from the epiblast stem cells (EpiSCs) to neural progenitor cells (NPCs), called the neural induction process, is crucial for cell fate determination of neural differentiation. However, the mechanism of this transition is unclear. Here, we identified a long non-coding RNA (linc1548) as a critical regulator of neural differentiation of mouse embryonic stem cells (mESCs). Knockout of linc1548 did not affect the conversion of mESCs to EpiSCs, but delayed the transition from EpiSCs to NPCs. Moreover, linc1548 interacts with the transcription factors OCT6 and SOX2 forming an RNA-protein complex to regulate the transition from EpiSCs to NPCs. Finally, we showed that Zfp521 is an important target gene of this RNA-protein complex regulating neural differentiation. Our findings prove how the intrinsic transcription complex is mediated by a lncRNA linc1548 and can better understand the intrinsic mechanism of neural fate determination.

Funder

Ministry of Science and Technology

National Natural Science Foundation of China

Shanghai Rising-Star Program

Fundamental Research Funds for the Central Universities

Matching Project Foundation of Shanghai University of Medicine and Health Sciences

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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