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DOI10.1126/science.aat6806
Dynamic DNA methylation: In the right place at the right time
Luo C.; Hajkova P.; Ecker J.R.
发表日期2018
ISSN0036-8075
起始页码1336
结束页码1340
卷号361期号:6409
英文摘要The classical model of cytosine DNA methylation (the presence of 5-methylcytosine, 5mC) regulation depicts this covalent modification as a stable repressive regulator of promoter activity. However, whole-genome analysis of 5mC reveals widespread tissue- and cell type–specific patterns and pervasive dynamics during mammalian development. Here we review recent findings that delineate 5mC functions in developmental stages and diverse genomic compartments as well as discuss the molecular mechanisms that connect transcriptional regulation and 5mC. Beyond the newly appreciated dynamics, regulatory roles for 5mC have been suggested in new biological contexts, such as learning and memory or aging. The use of new single-cell measurement techniques and precise editing tools will enable functional analyses of 5mC in gene expression, clarifying its role in various biological processes. © 2017 The Authors.
英文关键词5 methylcytosine; CRISPR associated endonuclease Cas9; cytosine; dioxygenase; DNA methyltransferase 3A; DNA methyltransferase 3B; histone H3; methyl CpG binding protein 2; RE1 silencing transcription factor; ten eleven translocation methylcytosine dioxygenase; transcription activator like effector; transcription factor; transcription factor CTCF; unclassified drug; zinc finger protein; 5 methylcytosine; transcription factor; biology; detection method; developmental biology; DNA; gene expression; genome; mammal; methylation; aging; developmental stage; DNA methylation; gene editing; gene expression; genetic transcription; genomics; human; hydroxymethylation; learning; memory; methylation; nonhuman; priority journal; Review; sequence analysis; single cell bisulfite sequencing; single cell reduced representation bisulfite sequencing; transcription regulation; animal; diseases; gene expression regulation; genetics; memory; metabolism; neoplasm; single cell analysis; Mammalia; 5-Methylcytosine; Aging; Animals; Disease; DNA Methylation; Gene Editing; Gene Expression Regulation, Developmental; Humans; Memory; Neoplasms; Single-Cell Analysis; Transcription Factors; Transcription, Genetic
语种英语
来源期刊Science
文献类型期刊论文
条目标识符http://gcip.llas.ac.cn/handle/2XKMVOVA/244597
作者单位Genomic Analysis Laboratory, Salk Institute for Biological Studies, San Diego, CA 92037, United States; Howard Hughes Medical Institute, Salk Institute for Biological Studies, San Diego, CA 92037, United States; MRC London Institute of Medical Sciences (LMS), Du Cane Road, London, W12 0NN, United Kingdom; Institute of Clinical Sciences (ICS), Faculty of Medicine, Imperial College London, Du Cane Road, London, W12 0NN, United Kingdom
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Luo C.,Hajkova P.,Ecker J.R.. Dynamic DNA methylation: In the right place at the right time[J],2018,361(6409).
APA Luo C.,Hajkova P.,&Ecker J.R..(2018).Dynamic DNA methylation: In the right place at the right time.Science,361(6409).
MLA Luo C.,et al."Dynamic DNA methylation: In the right place at the right time".Science 361.6409(2018).
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