SOX19b regulates the premature neuronal differentiation of neural stem cells through EZH2-mediated histone methylation in neural tube development of zebrafish

• Published in: Stem cell research & therapy Vol. 10; no. 1; p. 389
• Main Authors: Li, Xian, Zhou, Wenjuan, Li, Xinyue, Gao, Ming, Ji, Shufang, Tian, Wenyu, Ji, Guangyu, Du, Jingyi, Hao, Aijun
• Format: Journal Article
• Language: English
• Published: England BioMed Central Ltd 16.12.2019; BioMed Central; BMC
• Subjects: Analysis; Antisense oligonucleotides; ASCL1 protein; Binding sites; Birth defects; Brain; Cell cycle; Cell differentiation; Cell division; Central nervous system; Chromatin; Congenital defects; Criminal investigation; Cyclin-dependent kinase; Danio rerio; Embryo cells; Embryogenesis; Embryos; Epigenetic inheritance; Epigenetics; Forebrain; Gene expression; Genes; Hybridization; Immunoglobulins; Immunoprecipitation; Islet-1 protein; Methylation; Neural stem cells; Neural tube defects; Neurons; Pathogenesis; Phenotypes; Sox19b; Stem cells; Studies; Zebrafish; Beijing China; China; Neural stem cells; Zebrafish; Sox19b; Neural tube defects
• ISSN: 1757-6512; 1757-6512
• DOI: 10.1186/s13287-019-1495-3

Neural tube defects (NTDs) are the most serious and common birth defects in the clinic. The SRY-related HMG box B1 (SoxB1) gene family has been implicated in different processes of early embryogenesis. Sox19b is a maternally expressed gene in the SoxB1 family that is found in the region of the presumptive central nervous system (CNS), but its role and mechanism in embryonic neural stem cells (NSCs) during neural tube development have not yet been explored. Considering that Sox19b is specific to bony fish, we intended to investigate the role and mechanism of Sox19b in neural tube development in zebrafish embryos. Morpholino (MO) antisense oligonucleotides were used to construct a Sox19b loss-of-function zebrafish model. The phenotype and the expression of related genes were analysed by in situ hybridization and immunolabelling. Epigenetic modifications were detected by western blot and chromatin immunoprecipitation. In this study, we found that zebrafish embryos exhibited a reduced or even deleted forebrain phenotype after the expression of the Sox19b gene was inhibited. Moreover, we found for the first time that knockdown of Sox19b reduced the proliferation of NSCs; increased the transcription levels of Ngn1, Ascl1, HuC, Islet1, and cyclin-dependent kinase (CDK) inhibitors; and led to premature differentiation of NSCs. Finally, we found that knockdown of Sox19b decreased the levels of EZH2/H3K27me3 and decreased the level of H3K27me3 at the promoters of Ngn1 and ascl1a. Together, our data demonstrate that Sox19b plays an essential role in early NSC proliferation and differentiation through EZH2-mediated histone methylation in neural tube development. This study established the role of transcription factor Sox19b and epigenetic factor EZH2 regulatory network on NSC development, which provides new clues and theoretical guidance for the clinical treatment of neural tube defects.