雷特综合征
生物
表观遗传学
MECP2
遗传学
组蛋白
基因表达调控
基因
DNA甲基化
RNA聚合酶Ⅱ
基因表达
表型
发起人
作者
Christopher Wynder,Leanne Stalker,Martin L. Doughty
出处
期刊:Epigenomics
[Future Medicine]
日期:2010-06-01
卷期号:2 (3): 407-418
被引量:39
摘要
Significant neurological disorders can result from subtle perturbations of gene regulation that are often linked to epigenetic regulation. Proteins that regulate the methylation of lysine 4 of histone H3 (H3K4) and play a central role in epigenetic regulation, and mutations in genes encoding these enzymes have been identified in both autism and Rett syndrome. The H3K4 demethylases remove methyl groups from lysine 4 leading to loss of RNA polymerase binding and transcriptional repression. When these proteins are mutated, brain development is altered. Currently, little is known regarding how these gene regulators function at the genomic level. In this article, we will discuss findings that link H3K4 demethylases to neurodevelopment and neurological disease.
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