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SRX26293530: GSM8556093: PHILO, Arabidopsis, H3K9ac, 12cyc, rep1; Arabidopsis thaliana; ChIP-Seq
4 ILLUMINA (NextSeq 500) runs: 4.6M spots, 350.5M bases, 123.6Mb downloads

External Id: GSM8556093_r1
Submitted by: Rutgers State University of New Jersey
Study: High-throughput capture of transcription factor-driven chromatin dynamics using PHILO ChIP-seq [ChIP-seq 4]
show Abstracthide Abstract
Assessing the dynamics of chromatin and transcription factor (TF) DNA binding in plants remains a significant challenge, primarily due to the lack of efficient tools for capturing these features on a larger scale. Here, we present PHILO (Plant HIgh-throughput LOw input) ChIP-seq, a high-throughput ChIP-seq platform that enables the cost-effective and extensive capture of TF DNA binding and the genome-wide distribution of histone modifications. Through the application of H3K9ac PHILO ChIP-seq to eight jasmonic acid pathway mutants, involving the parallel processing of over 100 samples, we not only substantially corroborate the previously described interplay among chromatin regulators at the target genes of the JA master TF MYC2 but also unveil previously unknown histone acetylation patterns in the regulatory regions of MYC2 target genes. Overall, our PHILO ChIP-seq platform proves to be a highly effective approach for simultaneously examining chromatin on an unprecedented scale opening the door to conducting large-scale epigenome studies in plants. Overall design: ChIP-seq and PHILO ChIP-seq for histone modifications H3K9c, H3K4me3, H3K27me3, H3K36me3, transcription factor MYC2 and Pol II in Arabidopsis wildtype Col-0 seedlings and various jasmonic acid pathway mutants.
Sample: PHILO, Arabidopsis, H3K9ac, 12cyc, rep1
SAMN44064650 • SRS22822344 • All experiments • All runs
Library:
Name: GSM8556093
Instrument: NextSeq 500
Strategy: ChIP-Seq
Source: GENOMIC
Selection: ChIP
Layout: SINGLE
Construction protocol: Tissues were crosslinked with 1% formaldehyde solution for 2 x 10 min. After quenching, samples were shock-frozen, ground and chromatin was subsequently extracted. Chromatin was sonicated with a Diagenode Bioruptor. Libraries were prepared as follows. End repair (5 μl of End Repair Reaction Buffer + 2.5 μl of End Repair Enzyme Mix from the NEBNext End Repair Module (New England Biolabs)), A-tailing (2.5 µl NEBnext dA-Tailing Reaction Buffer + 1.5 µl Klenow Fragment (3'->5' exo-) (New England Biolabs)), adapter ligation (1 µl TruSeq DNA Unique Dual Indexes (UDIs) v2 (Illumina), 2.5 µl T4 DNA Ligase Reaction Buffer + 1.25 µl T4 DNA Ligase (New England Biolabs)), and PCR enrichment (12.5 µl NEBNext High-Fidelity 2X PCR Master Mix (New England Biolabs).
Runs: 4 runs, 4.6M spots, 350.5M bases, 123.6Mb
Run# of Spots# of BasesSizePublished
SRR308895281,160,39887.6M30.8Mb2024-12-02
SRR308895291,160,20787.6M30.9Mb2024-12-02
SRR308895301,162,82887.8M30.9Mb2024-12-02
SRR308895311,160,47787.6M31Mb2024-12-02

ID:
35501372

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