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神经管缺陷中叶酸缺乏导致的异常甲基化。

Abnormal methylation caused by folic acid deficiency in neural tube defects.

作者信息

Cao Rui, Xie Jun, Zhang Li

机构信息

Department of Biochemistry and Molecular Biology, Shanxi Key Laboratory of Birth Defect and Cell Regeneration, Key Laboratory for Cellular Physiology of Ministry of Education, Shanxi Medical University, No. 56, Xinjian South Road, Yingze District, Taiyuan, Shanxi Province, China.

Shanxi Key Laboratory of Pharmaceutical Biotechnology, Shanxi Biological Research Institute Co., Ltd, Taiyuan, China.

出版信息

Open Life Sci. 2022 Dec 22;17(1):1679-1688. doi: 10.1515/biol-2022-0504. eCollection 2022.

Abstract

Neural tube closure disorders, including anencephaly, spina bifida, and encephalocele, cause neural tube defects (NTDs). This congenital disability remained not only a major contributor to the prevalence of stillbirths and neonatal deaths but also a significant cause of lifelong physical disability in surviving infants. NTDs are complex diseases caused by multiple etiologies, levels, and mechanisms. Currently, the pathogenesis of NTDs is considered to be associated with both genetic and environmental factors. Here, we aimed to review the research progress on the etiology and mechanism of NTDs induced by methylation modification caused by folic acid deficiency. Folic acid supplementation in the diet is reported to be beneficial in preventing NTDs. Methylation modification is one of the most important epigenetic modifications crucial for brain neurodevelopment. Disturbances in folic acid metabolism and decreased -adenosylmethionine levels lead to reduced methyl donors and methylation modification disorders. In this review, we summarized the relationship between NTDs, folic acid metabolism, and related methylation of DNA, imprinted genes, cytoskeletal protein, histone, RNA, and non-coding RNA, so as to clarify the role of folic acid and methylation in NTDs and to better understand the various pathogenesis mechanisms of NTDs and the effective prevention.

摘要

神经管闭合障碍,包括无脑儿、脊柱裂和脑膨出,会导致神经管缺陷(NTDs)。这种先天性残疾不仅仍然是死产和新生儿死亡流行率的主要促成因素,也是存活婴儿终身身体残疾的重要原因。NTDs是由多种病因、层面和机制引起的复杂疾病。目前,NTDs的发病机制被认为与遗传和环境因素都有关。在此,我们旨在综述叶酸缺乏引起的甲基化修饰导致NTDs的病因和机制的研究进展。据报道,饮食中补充叶酸有助于预防NTDs。甲基化修饰是对脑神经元发育至关重要的最重要的表观遗传修饰之一。叶酸代谢紊乱和S-腺苷甲硫氨酸水平降低会导致甲基供体减少和甲基化修饰紊乱。在本综述中,我们总结了NTDs、叶酸代谢以及DNA、印记基因、细胞骨架蛋白、组蛋白、RNA和非编码RNA相关甲基化之间的关系,以阐明叶酸和甲基化在NTDs中的作用,并更好地理解NTDs的各种发病机制及有效预防措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fbe4/9784971/c320a6c2a0ff/j_biol-2022-0504-fig001.jpg

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