The effect of folic acid deficiency on FGF pathway via Brachyury regulation in neural tube defects. Issue 4 (28th December 2018)

• Record Type: Journal Article
• Authors: Chang, Shaoyan; Lu, Xiaolin; Wang, Shan; Wang, Zhigang; Huo, Junsheng; Huang, Jian; Shangguan, Shaofang; Li, Shen; Zou, Jizhen; Bao, Yihua; Guo, Jin; Wang, Fang; Niu, Bo; Zhang, Ting; Qiu, Zhiyong; Wu, Jianxin; Wang, Li
• Is Part Of: FASEB journal. Volume 33:Issue 4(2019)
• Page Start: 4688
• Page End: 4702
• Publication Date: 2018-12-28
• Subjects: T‐box transcription factor -- encephalocele -- mouse model -- neural development -- methylation modification; Biology -- Periodicals; Biology, Experimental -- Periodicals; 570
• DOI: 10.1096/fj.201801536R
• Languages: English
• ISSNs: 0892-6638

Abstract

ABSTRACT: Folate deficiency in early development leads to disturbance in multiple processes, including neurogenesis during which fibroblast growth factor (FGF) pathway is one of the crucial pathways. Whether folic acid (FA) directly affects FGF pathways to influence neurodevelopment and the possible mechanism remains unclear. In this study, we presented evidence that in human FA‐insufficient encephalocele, the FGF pathway was interfered. Furthermore, in Brachyury knockout mice devoid of such T‐box transcription factors regulating embryonic neuromesodermal bipotency and a key component of FGF pathway, change in expression of Brachyury downstream targets, activator Fgf8 and suppressor dual specificity phosphatase 6 was detected, along with the reduction in expression of other key FGF pathway genes. By using a FA‐deficient cell model, we further demonstrated that decrease in Brachyury expression was through alteration in hypermethylation at the Brachyury promoter region under FA deficiency conditions, and suppression of Brachyury promoted the inactivation of the FGF pathway. Correspondingly, FA supplementation partially reverses the effects seen in FA‐deficient embryoid bodies. Lastly, in mice with maternal folate‐deficient diets, aberrant FGF pathway activity was found in fetal brain dysplasia. Taken together, our findings highlight the effect of FA on FGF pathways during neurogenesis, and the mechanism may be due to the low expression of Brachyury gene via hypermethylation under FA‐insufficient conditions.—Chang, S., Lu, X., Wang, S., Wang, Z., Huo, J., Huang, J., Shangguan, S., Li, S., Zou, J., Bao, Y., Guo, J., Wang, F., Niu, B., Zhang, T., Qiu, Z., Wu, J., Wang, L. The effect of folic acid deficiency on FGF pathway via Brachyury regulation in neural tube defects. FASEB J. 33, 4688–4702 (2019). www.fasebj.org