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In Vivo ChIP-Seq of nuclear receptors: A rough guide to transform frozen tissues into high-confidence genome-wide binding profiles.
In: Nuclear Receptors. Berlin [u.a.]: Springer, 2019. 39-70 (Methods Mol. Biol. ; 1966)
Chromatin immunoprecipitation coupled to next generation sequencing (ChIP-seq) is a powerful tool to map context-dependent genome-wide binding of nuclear hormone receptors and their coregulators. This information can provide important mechanistic insight into where, when and how DNA–protein interactions are linked to target gene regulation. Here we describe a simple, yet reliable ChIP-seq method, including nuclear isolation from frozen tissue samples, cross-linking DNA–protein complexes, chromatin shearing, immunoprecipitation, and purification of ChIP DNA. We also include a standard ChIP-seq data analysis pipeline to elaborate and analyze raw single-end or paired-end sequencing data, including quality control steps, peak calling, annotation, and motif enrichment.
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Anmerkungen
Besondere Publikation
Auf Hompepage verbergern
Publikationstyp
Artikel: Sammelbandbeitrag/Buchkapitel
Schlagwörter
Chip-seq ; Chromatin Immunoprecipitation ; Data Analysis ; In Vivo ; Nuclear Receptors
Sprache
englisch
Veröffentlichungsjahr
2019
HGF-Berichtsjahr
2019
ISSN (print) / ISBN
1064-3745
e-ISSN
1940-6029
Bandtitel
Nuclear Receptors
Zeitschrift
Methods in Molecular Biology
Quellenangaben
Band: 1966,
Seiten: 39-70
Verlag
Springer
Verlagsort
Berlin [u.a.]
Begutachtungsstatus
Peer reviewed
Institut(e)
Institute of Diabetes and Cancer (IDC)
POF Topic(s)
90000 - German Center for Diabetes Research
Forschungsfeld(er)
Helmholtz Diabetes Center
PSP-Element(e)
G-501900-227
Scopus ID
85065419332
PubMed ID
31041738
Erfassungsdatum
2019-05-13