Impaired Generation of Mature Neurons Due to Extended Expression of Tlx by Repressing Sox2 Transcriptional Activity

Author:

Wang Yu12,Li Bin1,Dong Lianwei3,Duan Weibing45,Neuerburg Anna6,Zhang Han2,Jiang Xijuan1,Shao Rui4,Zhu Yan4,Bock Dagmar6,Liu Erwei2,Wang Hong1,Zhang Yunsha1,Dai Yifan78,Yang Haiyuan78,Wang Ying78ORCID

Affiliation:

1. School of Integrative Medicine  Tianjin University of Traditional Chinese Medicine, Tianjin, People's Republic of China

2. Laboratory of Pharmacology of TCM Formulae Co-Constructed by the Province-Ministry  Tianjin University of Traditional Chinese Medicine, Tianjin, People's Republic of China

3. Department of Cardiovascular Medicine  The People's Hospital of Ningxia Hui Autonomous Region, Yinchuan, People's Republic of China

4. Research and Development Center of TCM  Tianjin International Joint Academy of Biotechnology & Medicine, Tianjin, People's Republic of China

5. Jian Central People's Hospital, Jian, Jiangxi, People's Republic of China

6. Division of Molecular Biology of the Cell I  German Cancer Research Center (DKFZ), DKFZ-ZMBH Alliance, Heidelberg, Germany

7. Jiangsu Key Laboratory of Xenotransplantation  Nanjing Medical University, Nanjing, People's Republic of China

8. Key Laboratory of Targeted Intervention of Cardiovascular Disease, Collaborative Innovation Center for Cardiovascular Disease Translational Medicine  Nanjing Medical University, Nanjing, People's Republic of China

Abstract

Abstract As a master regulator of the dynamic process of adult neurogenesis, timely expression and regulation of the orphan nuclear receptor Tailless (Tlx) is essential. However, there is no study yet to directly investigate the essential role of precise spatiotemporal expressed Tlx. Here, we generated a conditional gain of Tlx expression transgenic mouse model, which allowed the extended Tlx expression in neural stem cells (NSCs) and their progeny by mating with a TlxCreERT2 mouse line. We demonstrate that extended expression of Tlx induced the impaired generation of mature neurons in adult subventricular zone and subgranular zone. Furthermore, we elucidated for the first time that this mutation decreased the endogenous expression of Sox2 by directly binding to its promoter. Restoration experiments further confirmed that Sox2 partially rescued these neuron maturation defects. Together, these findings not only highlight the importance of shutting-off Tlx on time in controlling NSC behavior, but also provide insights for further understanding adult neurogenesis and developing treatment strategies for neurological disorders.

Funder

The National Natural Science Foundation of China

The National Key R&D Program of China

The Program of International S&T Cooperation Project of China

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Developmental Biology,Molecular Medicine

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