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基因组印记、发育及疾病中的DNA甲基化

DNA methylation in genomic imprinting, development, and disease.

作者信息

Paulsen M, Ferguson-Smith A C

机构信息

University of Cambridge, Department of Anatomy, Cambridge CB2 3DY, UK.

出版信息

J Pathol. 2001 Sep;195(1):97-110. doi: 10.1002/path.890.

Abstract

Changes in DNA methylation profiles are common features of development and in a number of human diseases, such as cancer and imprinting disorders like Beckwith-Wiedemann and Prader-Willi/Angelman syndromes. This suggests that DNA methylation is required for proper gene regulation during development and in differentiated tissues and has clinical relevance. DNA methylation is also involved in X-chromosome inactivation and the allele-specific silencing of imprinted genes. This review describes possible mechanisms by which DNA methylation can regulate gene expression, using imprinted genes as examples. The molecular basis of methylation-mediated gene regulation is related to changes in chromatin structure and appears to be similar for both imprinted and biallelically expressed genes.

摘要

DNA甲基化谱的变化是发育过程以及许多人类疾病(如癌症和诸如贝克威思-维德曼综合征和普拉德-威利/安吉尔曼综合征等印记障碍)的共同特征。这表明DNA甲基化在发育过程中和分化组织中对于适当的基因调控是必需的,并且具有临床相关性。DNA甲基化还参与X染色体失活和印记基因的等位基因特异性沉默。本综述以印记基因为例,描述了DNA甲基化调控基因表达的可能机制。甲基化介导的基因调控的分子基础与染色质结构的变化有关,并且对于印记基因和双等位基因表达的基因似乎是相似的。

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