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智力迟钝的表观遗传机制。

Epigenetic mechanisms of mental retardation.

作者信息

Schaefer Anne, Tarakhovsky Alexander, Greengard Paul

机构信息

Laboratory of Molecular and Cellular Neuroscience, The Rockefeller University, 1230 York Avenue, New York, NY 10021, USA.

出版信息

Prog Drug Res. 2011;67:125-46. doi: 10.1007/978-3-7643-8989-5_7.

Abstract

Mental retardation is a common form of cognitive impairment affecting approximately 3% of the population in industrialized countries. The mental retardation syndrome incorporates a highly diverse group of mental disorders characterized by the combination of cognitive impairment and defective adaptive behavior. The genetic basis of the disease is strongly supported by identification of the genetic lesions associated with impaired cognition, learning, and social adaptation in many mental retardation syndromes. Several of the impaired genes encode epigenetic regulators of gene expression. These regulators exert their function through genome-wide posttranslational modification of histones or by mediating and/or recognizing DNA methylation. In this chapter, we review the most recent advances in the field of epigenetic mechanisms of mental retardation. In particular, we focus on animal models of the human diseases and the mechanism of transcriptional deregulation associated with changes in the cell epigenome.

摘要

智力迟钝是一种常见的认知障碍形式,在工业化国家约影响3%的人口。智力迟钝综合征包含一组高度多样化的精神障碍,其特征为认知障碍和适应性行为缺陷的结合。许多智力迟钝综合征中与认知、学习和社会适应受损相关的遗传病变的鉴定,有力地支持了该疾病的遗传基础。其中一些受损基因编码基因表达的表观遗传调节因子。这些调节因子通过全基因组组蛋白的翻译后修饰或通过介导和/或识别DNA甲基化来发挥其功能。在本章中,我们综述了智力迟钝表观遗传机制领域的最新进展。特别是,我们重点关注人类疾病的动物模型以及与细胞表观基因组变化相关的转录失调机制。

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