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SRX19210622: GSM7008932: HCK Input; Brassica rapa var. parachinensis; ChIP-Seq
1 ILLUMINA (Illumina NovaSeq 6000) run: 23.1M spots, 6.9G bases, 2.1Gb downloads

External Id: GSM7008932_r1
Submitted by: Beijing Academy of Agricultural and Forestry Sciences
Study: ChIP-seq using BrJMJ18-OX Par plants under NC and HS conditions
show Abstracthide Abstract
Using genome-wide pattern analysis and quantitative-trait-locus (QTL) mapping, we identified that a natural allele of BrJMJ18, BrJMJ18Par, encoding a novel H3K36me3/2 Jumonji demethylase, confers thermotolerance by delayed flowering and stimulated vegetative growth on B. rapa.To assess the downstream genes of BrJMJ18, we conducted a chromatin immunoprecipitation (ChIP) seq experiment using a polyclonal antibody recognizing BrJMJ18 in Par plants under normal conditon (LD, 21?) and high temperature condiation (LD, 28?), respectively. Overall design: Chromatin immunoprecipitation DNA-sequencing (ChIP-seq) for BrJMJ18-GFP in BrJMJ18 overexpresing Par plants. Par plants overexpressing tow allels of BrJMJ18, BrJMJ18WT (H1) and BrJMJ18Par (H2) were grown under low temperature (L, 21?) for 5 weeks or low temperature (L, 21?) for 4 weeks following with 1 week under high temperature (H, 28?), respectively. And wildtype Par plant was used as control (CK). The young and health leaves were collected for ChIP-seq. Two biological replicates were performed for each sample.
Sample: HCK Input
SAMN32954046 • SRS16617948 • All experiments • All runs
Library:
Name: GSM7008932
Instrument: Illumina NovaSeq 6000
Strategy: ChIP-Seq
Source: GENOMIC
Selection: ChIP
Layout: PAIRED
Construction protocol: 1.5 g samples were washed twice in cold phosphate-buffered saline (PBS), cross-linked with 1% formaldehyde for 10 minutes at room temperature, and then quenched by the addition of glycine (125 mmol/L final concentration). Afterwards, samples were lysed and chromatin was obtained on ice. Chromatin was sonicated to get soluble sheared chromatin (average DNA length of 200–500 bp). ChIP-seq libraries were prepared using the KAPA HTP Library Preparation Kit complemented with NEXTflex DNA Barcodes from Bioo Scientific. 10 ng of DNA was used as starting material for input and ip samples. Libraries were amplified using 13 cycles on the thermocycler. Post amplification libraries were size selected at 250-450bp in length using Agencourt AMPure XP beads from Beckman Coulter. Libraries were validated using the Agilent High Sensitivity DNA Kit.
Runs: 1 run, 23.1M spots, 6.9G bases, 2.1Gb
Run# of Spots# of BasesSizePublished
SRR2326643823,061,6546.9G2.1Gb2024-01-31

ID:
26413315

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