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Status |
Public on Nov 15, 2017 |
Title |
Chromatin immunoprecipitation for genome-wide mapping of endogenous G-quadruplex DNA structures |
Organism |
Homo sapiens |
Experiment type |
Genome binding/occupancy profiling by high throughput sequencing
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Summary |
G-rich DNA sequences can form four-stranded G-quadruplex (G4) secondary structures and are linked to fundamental biological processes such as transcription, replication and telomere maintenance. G4s are also implicated in promoting genome instability, cancer and other diseases. Here, we describe a detailed G4 ChIP-seq method that robustly enables the determination of G4 structure formation genome-wide in chromatin. This protocol adapts traditional ChIP-seq for the detection of DNA secondary structures through the use of a G4-structure-specific phage display antibody with refinements in chromatin immunoprecipitation followed by high-throughput sequencing. Beginning with chromatin isolation and antibody preparation the entire protocol can be completed in less than 1 week including computational analysis.
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Overall design |
One cell line analysed with G4 ChIP-seq to detect the presence of G-Quadruplexes. Experiment performed in triplicates.
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Contributor(s) |
Hänsel-Hertsch R, Spiegel J, Marsico G, Tannahill D, Balasubramanian S |
Citation missing |
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Submission date |
May 23, 2017 |
Last update date |
May 15, 2019 |
Contact name |
Giovanni Marsico |
E-mail(s) |
persego@gmail.com
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Organization name |
CRUK Cambridge Institute
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Street address |
Robinson Way
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City |
Cambridge |
ZIP/Postal code |
CB2 0RE |
Country |
United Kingdom |
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Platforms (1) |
GPL18573 |
Illumina NextSeq 500 (Homo sapiens) |
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Samples (4)
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Relations |
BioProject |
PRJNA387558 |
SRA |
SRP107851 |