Non-CG DNA methylation in animal genomes

IF 29 1区 生物学 Q1 GENETICS & HEREDITY
Thirsa Brethouwer, Alex de Mendoza, Ozren Bogdanovic
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引用次数: 0

Abstract

Cytosine DNA methylation is widespread in animal genomes and occurs predominantly at CG dinucleotides (mCG). While the roles of mCG, such as in genomic imprinting and genome stability, are well established, non-CG DNA methylation (mCH) remains poorly understood. In most vertebrate tissues, roughly 80% of CGs are methylated, whereas mCH levels are generally low, typically ranging from 1% to 3%. In vertebrates, mCH is most prevalent in neural tissue, oocytes and embryonic stem cells and has been linked to neurodevelopmental disorders. Moreover, mCH appears to have a conserved role in regulating vertebrate neural genomes, and recent studies suggest that it has functions in the embryogenesis of teleost fish. Overall, mCH represents an intriguing emerging aspect of gene regulation with potential implications for cellular identity, repeat silencing and neural function. In this Review, we provide a critical overview of the patterning, mechanisms and functional implications of mCH in animals.

Abstract Image

动物基因组中的非cg DNA甲基化
胞嘧啶DNA甲基化在动物基因组中广泛存在,主要发生在CG二核苷酸(mCG)上。虽然mCG在基因组印迹和基因组稳定性等方面的作用已经得到了很好的证实,但对非cg DNA甲基化(mCH)的了解仍然很少。在大多数脊椎动物组织中,大约80%的CGs被甲基化,而mCH水平普遍较低,通常在1%至3%之间。在脊椎动物中,多氯甲烷在神经组织、卵母细胞和胚胎干细胞中最为普遍,并与神经发育障碍有关。此外,mCH似乎在调节脊椎动物神经基因组中具有保守作用,最近的研究表明它在硬骨鱼的胚胎发生中具有功能。总的来说,mCH代表了基因调控的一个有趣的新兴方面,对细胞身份、重复沉默和神经功能有潜在的影响。在这篇综述中,我们对动物中mCH的模式、机制和功能意义进行了综述。
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来源期刊
Nature genetics
Nature genetics 生物-遗传学
CiteScore
43.00
自引率
2.60%
发文量
241
审稿时长
3 months
期刊介绍: Nature Genetics publishes the very highest quality research in genetics. It encompasses genetic and functional genomic studies on human and plant traits and on other model organisms. Current emphasis is on the genetic basis for common and complex diseases and on the functional mechanism, architecture and evolution of gene networks, studied by experimental perturbation. Integrative genetic topics comprise, but are not limited to: -Genes in the pathology of human disease -Molecular analysis of simple and complex genetic traits -Cancer genetics -Agricultural genomics -Developmental genetics -Regulatory variation in gene expression -Strategies and technologies for extracting function from genomic data -Pharmacological genomics -Genome evolution
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