From profiles to function in epigenomics

被引:189
作者
Stricker, Stefan H. [1 ,2 ]
Koferle, Anna [3 ]
Beck, Stephan [3 ]
机构
[1] German Res Ctr Environm Hlth, Inst Stem Cell Res, Ingolstadter Landstr 1, D-85764 Neuherberg, Germany
[2] Ludwig Maximilians Univ Munchen, Biomed Ctr, Grosshaderner Str 9, D-82152 Planegg Martinsried, Germany
[3] UCL, Inst Canc, Paul OGorman Bldg,72 Huntley St, London WC1E 6BT, England
关键词
DE-NOVO METHYLATION; DNA METHYLATION; EPIGENETIC REGULATION; GENE-EXPRESSION; HISTONE DEACETYLASE-1; TRANSCRIPTION FACTORS; LYSINE METHYLATION; CELL DEVELOPMENT; GENOME; MOUSE;
D O I
10.1038/nrg.2016.138
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Myriads of epigenomic features have been comprehensively profiled in health and disease across cell types, tissues and individuals. Although current epigenomic approaches can infer function for chromatin marks through correlation, it remains challenging to establish which marks actually have causative roles in gene regulation and other processes. After revisiting how classical approaches have addressed this question in the past, we discuss the current state of epigenomic profiling and how functional information can be indirectly inferred. We also present new approaches that promise definitive functional answers, which are collectively referred to as `epigenome editing'. In particular, we explore CRISPR-based technologies for single-locus and multi-locus manipulation. Finally, we discuss which level of function can be achieved with each approach and introduce emerging strategies for high-throughput progression from profiles to function.
引用
收藏
页码:51 / 66
页数:16
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