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Stricker, S.H. ; Köferle, A.* ; Beck, S.*

From profiles to function in epigenomics.

Nat. Rev. Genet. 18, 51-66 (2017)
Verlagsversion Postprint Forschungsdaten DOI
Open Access Green
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.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Review
Schlagwörter Chromatin analysis; CRISPR-Cas systems; DNA methylation; Epigenetics; Epigenomics; Gene regulation; Genetic engineering; Histone post-translational modifications; Targeted Dna Methylation; De-novo Methylation; Epigenetic Regulation; Gene-expression; Transcriptional Regulation; Histone Deacetylase-1; Mammalian Development; Cell Differentiation; Early Embryogenesis; Lysine Methylation
Sprache englisch
Veröffentlichungsjahr 2017
Prepublished im Jahr 2016
HGF-Berichtsjahr 2016
ISSN (print) / ISBN 1471-0056
e-ISSN 1471-0064
Zeitschrift Nature Reviews - Genetics
Quellenangaben Band: 18, Heft: 1, Seiten: 51-66 Artikelnummer: , Supplement: ,
Verlag Nature Publishing Group
Verlagsort London
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Stem Cell Research (ISF)
POF Topic(s) 30204 - Cell Programming and Repair
Forschungsfeld(er) Stem Cell and Neuroscience
PSP-Element(e) G-500800-001
DOI 10.1038/nrg.2016.138
WOS ID WOS:000393268300009
Erfassungsdatum 2016-11-22
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